CA2174107C - Esters of substituted-hydroxyacetyl piperazine phenyl oxazolidinones - Google Patents
Esters of substituted-hydroxyacetyl piperazine phenyl oxazolidinones Download PDFInfo
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- CA2174107C CA2174107C CA002174107A CA2174107A CA2174107C CA 2174107 C CA2174107 C CA 2174107C CA 002174107 A CA002174107 A CA 002174107A CA 2174107 A CA2174107 A CA 2174107A CA 2174107 C CA2174107 C CA 2174107C
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- piperazinyl
- oxo
- methyl
- oxazolidinyl
- acetylamino
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/08—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D263/16—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D263/18—Oxygen atoms
- C07D263/20—Oxygen atoms attached in position 2
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6558—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
- C07F9/65583—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system each of the hetero rings containing nitrogen as ring hetero atom
Abstract
A compound of structural Formula (1) or pharmaceutically acceptable salts thereof wherein: R is -C(O)-R1, -PO3= or -P(O)(OH)2;
R1 is C1-6 alkyl, -N(R4)2, C1-6 alkyl-N(R4)2, -phenyl-N(R4)2, -phenyl-NHC(O)CH2NH2,-C2H4-morpholinyl, pyridinyl, C1-6 alkyl-OH, C1-6 alkyl-OCH3, C1-6 alkyl C(O)CH3, -O-C1-6 alkyl-OCH3, C0-3 alkyl-piperazinyl (optionally substituted with C1-3 alkyl), imidazolyl, C1-6 alkyl-COOH, -C(CH2OH)2CH3; R2 and R3 are independently selected from hydrogen or F except at least one of R2 or R3 is F; R4 are independently selected from hydrogen or C1-6 alkyl. The compounds are water soluble and are useful antimicrobial agents, effective against a number of human and veterinary pathogens, including multiply-resistant staphylococci, enterococci and streptococci, as well as anaerobic organisms such as bacteriodes and clostridia species, and acid-fast organisms such as Mycobacterium tuberculosis.
R1 is C1-6 alkyl, -N(R4)2, C1-6 alkyl-N(R4)2, -phenyl-N(R4)2, -phenyl-NHC(O)CH2NH2,-C2H4-morpholinyl, pyridinyl, C1-6 alkyl-OH, C1-6 alkyl-OCH3, C1-6 alkyl C(O)CH3, -O-C1-6 alkyl-OCH3, C0-3 alkyl-piperazinyl (optionally substituted with C1-3 alkyl), imidazolyl, C1-6 alkyl-COOH, -C(CH2OH)2CH3; R2 and R3 are independently selected from hydrogen or F except at least one of R2 or R3 is F; R4 are independently selected from hydrogen or C1-6 alkyl. The compounds are water soluble and are useful antimicrobial agents, effective against a number of human and veterinary pathogens, including multiply-resistant staphylococci, enterococci and streptococci, as well as anaerobic organisms such as bacteriodes and clostridia species, and acid-fast organisms such as Mycobacterium tuberculosis.
Description
4718.P CP
ESTERS OF SUBSTITUTED-HYDROXYACETYL PIPERAZINE PHENYL
Background of the Invention The subject invention discloses carboxylic and phosphate esters of substituted-hydroxyacetyl piperazine phenyl oxazolidinones. The compounds and their salts are water soluble which makes them particularly useful for IV and oral administration for the treatment of microbial infections. The compounds are effective against a number of human and veterinary pathogens, including multiply-resistant staphylococci, enterococci and streptococci, as well as anaerobic organisms such as bacteroides and clostridia species, and acid-fast organisms such as Mycobacterium tuberculosis. The compounds are particularly useful because they are effective against the latter organism which is known to be responsible for infection in persons with AIDS. Information Disclosure Statement US Patents 5,164,510 and related 5,225,565 and 5,182,403 discloses 5'indolinyl-513-amidomethyloxazolidinones, 3-(fused-ring substituted)phenyl-5B-amidomethyloxazolidinones, and 3-(nitrogen substituted)phenyl-5!3-amidomethyl-oxazolidinones which are useful as antibacterial agents.
WO 93/23384 discloses hydroxyacetyl diazene phenyl oxazolidinones similar to the subject compounds except that the subject compounds are substituted with carboxylic and phosphate esters (i.e., R is -C(O)-Ri, -P03' or -P(O)(OH)2) and are water soluble.
Other references disclosing various oxazolidinones include US Patent 4,801,600, 4,921,869, Gregory W. A., et al., J. Med. Chem., 32, 1673-81 ( 1989);
Gregory W. A., et al., J. Med. Chem., 33, 2569-78 (1990); Wang C., et al., Tetrahedron. 45, 1323-26 ( 1989); and Brittelli, et al., J. Med. Chem., 35, 1156 ( 1992).
European Patent Publication 352,781 discloses phenyl and pyridyl substituted phenyl oxazolidinones.
European Patent Publication 316,594 discloses 3-substituted styryl oxazolidinones.
European Patent Publication 312,000 discloses phenylmethyl and pyridinylmethyl substituted phenyl oxazolidinones.
. WO 95/14684 PCT/US94/10582 Summary of the Invention In one aspect, the subject invention is a compound of structural Formula I:
H
R-O' /C ~N ~ ~ N~ ~~N-,C-CH
or pharmaceutically acceptable salts thereof wherein:
R is -C(O)-Rl, -POs= or -P(O)(OH)2;
Rl is Cl_s alkyl, -N(R4)2, C1_s alkyl-N(R4)2, -Phenyl-N(R4)2, -phenyl-NHC(O)CH2NH2, -C2H4-morpholinyl, pyridinyl, C1_6 alkyl-OH, C1_s alkyl-OCHs, C1_ salkyl C(O)CH3~ -O-C1_s alkyl-OCHs, Co_3 alkyl-piperazinyl (optionally substituted with C1_~ alkyl), imidazolyl, C1_s alkyl-COOH, -C(CH20H)2CHs;
RZ and R3 are independently selected from hydrogen or F, except at least one of R2 or R3 is F;
R4 are independently selected from hydrogen or Cl_s alkyl.
Preferred compounds of the subject invention are where R is -C(O)-R1 and Rl is -CHs, -CH2N(CHs)2, -C2H4-morpholinyl or -CH20H. Even more preferred is where the compound is an optically pure enantiomer having the S- configuration at C5 of the oxazolidinone ring.
More preferable is where one of R2 and Rs is F and the other is hydrogen.
In another aspect, the subject invention is directed toward a method for treating microbial infections in warm blooded animals by administering to a warm blooded animal in need thereof an effective amount of a compound of Formula I
as described above. Preferably, the compound is administered in an amount of from about 0.1 to about 100 mglkg of body weight/day, more preferably, from about 3.0 to about 50 mg/kg of body weight/day.
Detailed Description of the Invention The present invention discloses carboxylic and phosphate esters of substituted-hyroxyacetyl piperazinyl phenyl oxazolidinones of structural Formula I
as defined above. The compounds are useful antimicrobial agents, effective against a number of human and veterinary pathogens, including multiply-resistant staphylococci, enterococci and streptococci, as well as anaerobic organisms such as __ , ~, R'O 95/14684 . ~ ~ f~ PCT/US94/10582 .
_3_ bacteroides and clostridia species, and acid-fast bacteria such as Mycobacterium tuberculosis. The compounds are designed to be aqueous soluble such that they can be administered by intravenous or oral means.
With respect to the above definition, C1_s alkyl is methyl, ethyl, propyl, butyl, pentyl, hexyl and isomeric forms thereof.
Pharmaceutically acceptable salts means salts useful for administering the compounds of this invention and include hydrochloride, hydrobromide, hydroiodide, sulfate, phosphate, acetate, propionate, lactate, mesylate, maleate, malate, succinate, tartxate, citric acid, 2-hydroxyethyl sulfonate, fumarate, sodium or potassium, ammonioum salt and the like. These salts may be in hydrated form.
The most preferred compounds of the series would be prepared as the optically pure enantiomers having the (S)-configuration at C5 of the oxazolidinone ring. More preferably the compounds have only one of either R2 and R3 as fluorine.
The compounds of this invention have an aqueous solubility of greater than 1 mg/ml, more preferably, greater than 4 mg/r :.
Optically pure material could be obtained either by one of a number of asymmetric syntheses or alternatively by resolution from a racemic mixture by selective crystallization of a salt from, for example, intermediate amine 12 (as described in Example 1) with an appropriate optically active acid such as dibenzoyl tartrate or 10-camphorsulfonic acid, followed by treatment with base to afford the optically pure amine.
Commercially available difluoronitrobenzene is treated with excess piperazine to afford a displacement product. Reduction of the vitro group with the ammonium formate-Pd/C reagent system or hydrogen-Pd/C affords an aniline derivative.
Protection of this aniline derivative affords a bis-(benzyloxy carbonyl) (CBZ) derivative which is treated with nBuLi in THF or ether at -78 to -15°C, then R-glycidyl butyrate is added, and the mixture stirred overnight at 20°C, to give optically active 5-(R)-hydroxy methyl oxazolidinone. Mesylation of 5-(R)-hydroxy methyl oxazolidinone under classical conditions affordes a mesylate which undergoes smooth displacement with sodium azide to form an azide. Reduction of the azide by hydrogenation over Pd/C gives an amine which can be acylated in situ with acetic anhydride and pyridine to afforded a CBZ-protected oxazolidinone intermediate, (S)-N-3-((3-fluoro-4-(4-(carbobenzyloxy)-1-piperazinyl)phenyl)-2-oxo-5-oxazolidinyl)methyl)acetamide. More preferred, the aminomethyloxazolidinone is prepared by displacement of the mesylate with potassium phthalimide to give a phthalimide. Treatment of this phthalimide with aqueous methylamine gives the WO 95/14684 ' , - , , PCT/US94/10582 amine.
Deprotection of the N-carbobenzyloxy with Pd/C and hydrogen afforded the key intermediate for analog preparation, (S)-N-3-((3-fluoro-4-(1-piperazinyl)phenyl)-2-oxo-5-oxazolidinyl)methyl)acetamide (22).
These compounds are useful for treatment of microbial infections in humans and other warm blooded animals, under both parenteral, topical and oral administration.
The pharmaceutical compositions of this invention may be prepared by combining the compounds of Formula I of this invention with a solid or liquid pharmaceutically acceptable carrier and, optionally, with pharmaceutically acceptable adjuvants and excipients employing standard and conventional techniques. Solid form compositions include powders, tablets, dispersible granules, capsules, cachets and suppositories. A solid carrier can be at least one substance which may also function as a diluent, flavoring agent, solubilizer, lubricant, suspending agent, binder, tablet disintegrating agent, and encapsulating agent.
Inert solid carriers include magnesium carbonate, magnesium stearate, talc, sugar, lactose, pectin, dextrin, starch, gelatin, cellulosic materials, low melting wax, cocoa butter, and the like. Liquid form compositions include solutions, suspensions and emulsions. For example, there may be provided solutions of the compounds of this invention dissolved in water and water-propylene glycol and water-polyethylene glycol systems, optionally containing suitable conventional coloring agents, flavoring agents, stabilizers and thickening agents.
Preferably, the pharmaceutical composition is provided employing conventional techniques in unit dosage form containing effective or appropriate amounts of the active component, that is, the compound of Formula I according to this invention.
The quantity of active component, that is the compound of Formula I
according to this invention, in the pharmaceutical composition and unit dosage form thereof may be varied or adjusted widely depending upon the particular application, the potency of the particular compound, the desired concentration. Generally, the quantity of active component will range between 0.5% to 90% by weight of the composition.
In therapeutic use for treating, or combatting, bacterial infections in warm-blooded animals, the compounds or pharmaceutical compositions thereof will be administered orally and/or parenterally at a dosage to obtain and maintain a concentration, that is, an amount, or blood-level of active component in the animal WO 95/14684. ~ ~ PCT/US94/10582 undergoing treatment which will be antibacterially effective. Generally, such antibacterially effective amount of dosage of active component will be in the range of about 0.1 to about 100, more preferably about 3.0 to about 50 mg/kg of body weightJday. It is to be understood that the dosages may vary depending upon the requirements of the patient, the severity of the bacterial infection being treated, and the particular compound being used. Also, it is to be understood that the initial dosage administered may be increased beyond the above upper level in order to rapidly achieve the desired blood-level or the initial dosage may be smaller than the optimum and the daily dosage may be progressively increased during the course of treatment depending on the particular situation. If desired, the daily dose may also be divided into multiple doses for administration, e.g., two to four times per day.
The compounds of Formula I according to this invention are administered parenterally, i.e., by injection, for example, by intravenous injection or by other parenteral routes of administration. Pharmaceutical compositions for parenteral administration will generally contain a pharmaceutically acceptable amount of the compound according to Formula I as a soluble salt (acid addition salt or base salt) dissolved i.n a pharmaceutically acceptable liquid carrier such as, for example, water-for-injection and a buffer to provide a suitably buffered isotonic solution, for example, having a pH of about 3-7. Suitable buffering agents include, for example, trisodium orthophosphate, sodium bicarbonate, sodium citrate, N-methylglucamine, L(+)-lysine and L(+)-arginine to name but a few representative buffering agents.
The compound according to Formula I generally will be dissolved in the carrier in an amount sufficient to provide a pharmaceutically acceptable injectable concentration in the range of about 1 mg/ml to about 400 mg/ml of solution. The resulting liquid pharmaceutical composition will be administered so as to obtain the above-mentioned antibacterially effective amount of dosage. The compounds of Formula I
according to this invention, due to their aqueous solubility, are advantageously administered orally in solid and liquid dosage forms.
Antimicrobial activity was tested in vivo using the Murine Assay procedure.
Groups of female mice (six mice of 18-20 grams each) were injected intraperitoneally with bacteria which were thawed just prior to use and suspended in brain heart infusion with 4% brewers yeast UC8213 (Staphylococcus aureus) or brain heart infusion (Streptococcus species). Antibiotic treatment at six dose levels per drug was administered one hour and five hours after infection by either oral intubation or subcutaneous ("subcut.") routes. Survival was observed daily for six days.
ED5o values based on mortality ratios were calculated using probit analysis. The subject ,.
. WO 95/14684 PCT/LTS94/10582 compounds were compared against a well-known antimicrobial (Vancomycin) as a control. The data are shown in Table 1.
i WO 95114684. ~ ~ t~ PCTlUS94/1o582 ' _7_ In Vivo Activity of Examples VANCOMYCIN EDso Example ED mg/kg mg/kg (subcut.) ROUTE
1 5/4 2 oral/subcut.
2 9/15 5 oral/subcut.
ESTERS OF SUBSTITUTED-HYDROXYACETYL PIPERAZINE PHENYL
Background of the Invention The subject invention discloses carboxylic and phosphate esters of substituted-hydroxyacetyl piperazine phenyl oxazolidinones. The compounds and their salts are water soluble which makes them particularly useful for IV and oral administration for the treatment of microbial infections. The compounds are effective against a number of human and veterinary pathogens, including multiply-resistant staphylococci, enterococci and streptococci, as well as anaerobic organisms such as bacteroides and clostridia species, and acid-fast organisms such as Mycobacterium tuberculosis. The compounds are particularly useful because they are effective against the latter organism which is known to be responsible for infection in persons with AIDS. Information Disclosure Statement US Patents 5,164,510 and related 5,225,565 and 5,182,403 discloses 5'indolinyl-513-amidomethyloxazolidinones, 3-(fused-ring substituted)phenyl-5B-amidomethyloxazolidinones, and 3-(nitrogen substituted)phenyl-5!3-amidomethyl-oxazolidinones which are useful as antibacterial agents.
WO 93/23384 discloses hydroxyacetyl diazene phenyl oxazolidinones similar to the subject compounds except that the subject compounds are substituted with carboxylic and phosphate esters (i.e., R is -C(O)-Ri, -P03' or -P(O)(OH)2) and are water soluble.
Other references disclosing various oxazolidinones include US Patent 4,801,600, 4,921,869, Gregory W. A., et al., J. Med. Chem., 32, 1673-81 ( 1989);
Gregory W. A., et al., J. Med. Chem., 33, 2569-78 (1990); Wang C., et al., Tetrahedron. 45, 1323-26 ( 1989); and Brittelli, et al., J. Med. Chem., 35, 1156 ( 1992).
European Patent Publication 352,781 discloses phenyl and pyridyl substituted phenyl oxazolidinones.
European Patent Publication 316,594 discloses 3-substituted styryl oxazolidinones.
European Patent Publication 312,000 discloses phenylmethyl and pyridinylmethyl substituted phenyl oxazolidinones.
. WO 95/14684 PCT/US94/10582 Summary of the Invention In one aspect, the subject invention is a compound of structural Formula I:
H
R-O' /C ~N ~ ~ N~ ~~N-,C-CH
or pharmaceutically acceptable salts thereof wherein:
R is -C(O)-Rl, -POs= or -P(O)(OH)2;
Rl is Cl_s alkyl, -N(R4)2, C1_s alkyl-N(R4)2, -Phenyl-N(R4)2, -phenyl-NHC(O)CH2NH2, -C2H4-morpholinyl, pyridinyl, C1_6 alkyl-OH, C1_s alkyl-OCHs, C1_ salkyl C(O)CH3~ -O-C1_s alkyl-OCHs, Co_3 alkyl-piperazinyl (optionally substituted with C1_~ alkyl), imidazolyl, C1_s alkyl-COOH, -C(CH20H)2CHs;
RZ and R3 are independently selected from hydrogen or F, except at least one of R2 or R3 is F;
R4 are independently selected from hydrogen or Cl_s alkyl.
Preferred compounds of the subject invention are where R is -C(O)-R1 and Rl is -CHs, -CH2N(CHs)2, -C2H4-morpholinyl or -CH20H. Even more preferred is where the compound is an optically pure enantiomer having the S- configuration at C5 of the oxazolidinone ring.
More preferable is where one of R2 and Rs is F and the other is hydrogen.
In another aspect, the subject invention is directed toward a method for treating microbial infections in warm blooded animals by administering to a warm blooded animal in need thereof an effective amount of a compound of Formula I
as described above. Preferably, the compound is administered in an amount of from about 0.1 to about 100 mglkg of body weight/day, more preferably, from about 3.0 to about 50 mg/kg of body weight/day.
Detailed Description of the Invention The present invention discloses carboxylic and phosphate esters of substituted-hyroxyacetyl piperazinyl phenyl oxazolidinones of structural Formula I
as defined above. The compounds are useful antimicrobial agents, effective against a number of human and veterinary pathogens, including multiply-resistant staphylococci, enterococci and streptococci, as well as anaerobic organisms such as __ , ~, R'O 95/14684 . ~ ~ f~ PCT/US94/10582 .
_3_ bacteroides and clostridia species, and acid-fast bacteria such as Mycobacterium tuberculosis. The compounds are designed to be aqueous soluble such that they can be administered by intravenous or oral means.
With respect to the above definition, C1_s alkyl is methyl, ethyl, propyl, butyl, pentyl, hexyl and isomeric forms thereof.
Pharmaceutically acceptable salts means salts useful for administering the compounds of this invention and include hydrochloride, hydrobromide, hydroiodide, sulfate, phosphate, acetate, propionate, lactate, mesylate, maleate, malate, succinate, tartxate, citric acid, 2-hydroxyethyl sulfonate, fumarate, sodium or potassium, ammonioum salt and the like. These salts may be in hydrated form.
The most preferred compounds of the series would be prepared as the optically pure enantiomers having the (S)-configuration at C5 of the oxazolidinone ring. More preferably the compounds have only one of either R2 and R3 as fluorine.
The compounds of this invention have an aqueous solubility of greater than 1 mg/ml, more preferably, greater than 4 mg/r :.
Optically pure material could be obtained either by one of a number of asymmetric syntheses or alternatively by resolution from a racemic mixture by selective crystallization of a salt from, for example, intermediate amine 12 (as described in Example 1) with an appropriate optically active acid such as dibenzoyl tartrate or 10-camphorsulfonic acid, followed by treatment with base to afford the optically pure amine.
Commercially available difluoronitrobenzene is treated with excess piperazine to afford a displacement product. Reduction of the vitro group with the ammonium formate-Pd/C reagent system or hydrogen-Pd/C affords an aniline derivative.
Protection of this aniline derivative affords a bis-(benzyloxy carbonyl) (CBZ) derivative which is treated with nBuLi in THF or ether at -78 to -15°C, then R-glycidyl butyrate is added, and the mixture stirred overnight at 20°C, to give optically active 5-(R)-hydroxy methyl oxazolidinone. Mesylation of 5-(R)-hydroxy methyl oxazolidinone under classical conditions affordes a mesylate which undergoes smooth displacement with sodium azide to form an azide. Reduction of the azide by hydrogenation over Pd/C gives an amine which can be acylated in situ with acetic anhydride and pyridine to afforded a CBZ-protected oxazolidinone intermediate, (S)-N-3-((3-fluoro-4-(4-(carbobenzyloxy)-1-piperazinyl)phenyl)-2-oxo-5-oxazolidinyl)methyl)acetamide. More preferred, the aminomethyloxazolidinone is prepared by displacement of the mesylate with potassium phthalimide to give a phthalimide. Treatment of this phthalimide with aqueous methylamine gives the WO 95/14684 ' , - , , PCT/US94/10582 amine.
Deprotection of the N-carbobenzyloxy with Pd/C and hydrogen afforded the key intermediate for analog preparation, (S)-N-3-((3-fluoro-4-(1-piperazinyl)phenyl)-2-oxo-5-oxazolidinyl)methyl)acetamide (22).
These compounds are useful for treatment of microbial infections in humans and other warm blooded animals, under both parenteral, topical and oral administration.
The pharmaceutical compositions of this invention may be prepared by combining the compounds of Formula I of this invention with a solid or liquid pharmaceutically acceptable carrier and, optionally, with pharmaceutically acceptable adjuvants and excipients employing standard and conventional techniques. Solid form compositions include powders, tablets, dispersible granules, capsules, cachets and suppositories. A solid carrier can be at least one substance which may also function as a diluent, flavoring agent, solubilizer, lubricant, suspending agent, binder, tablet disintegrating agent, and encapsulating agent.
Inert solid carriers include magnesium carbonate, magnesium stearate, talc, sugar, lactose, pectin, dextrin, starch, gelatin, cellulosic materials, low melting wax, cocoa butter, and the like. Liquid form compositions include solutions, suspensions and emulsions. For example, there may be provided solutions of the compounds of this invention dissolved in water and water-propylene glycol and water-polyethylene glycol systems, optionally containing suitable conventional coloring agents, flavoring agents, stabilizers and thickening agents.
Preferably, the pharmaceutical composition is provided employing conventional techniques in unit dosage form containing effective or appropriate amounts of the active component, that is, the compound of Formula I according to this invention.
The quantity of active component, that is the compound of Formula I
according to this invention, in the pharmaceutical composition and unit dosage form thereof may be varied or adjusted widely depending upon the particular application, the potency of the particular compound, the desired concentration. Generally, the quantity of active component will range between 0.5% to 90% by weight of the composition.
In therapeutic use for treating, or combatting, bacterial infections in warm-blooded animals, the compounds or pharmaceutical compositions thereof will be administered orally and/or parenterally at a dosage to obtain and maintain a concentration, that is, an amount, or blood-level of active component in the animal WO 95/14684. ~ ~ PCT/US94/10582 undergoing treatment which will be antibacterially effective. Generally, such antibacterially effective amount of dosage of active component will be in the range of about 0.1 to about 100, more preferably about 3.0 to about 50 mg/kg of body weightJday. It is to be understood that the dosages may vary depending upon the requirements of the patient, the severity of the bacterial infection being treated, and the particular compound being used. Also, it is to be understood that the initial dosage administered may be increased beyond the above upper level in order to rapidly achieve the desired blood-level or the initial dosage may be smaller than the optimum and the daily dosage may be progressively increased during the course of treatment depending on the particular situation. If desired, the daily dose may also be divided into multiple doses for administration, e.g., two to four times per day.
The compounds of Formula I according to this invention are administered parenterally, i.e., by injection, for example, by intravenous injection or by other parenteral routes of administration. Pharmaceutical compositions for parenteral administration will generally contain a pharmaceutically acceptable amount of the compound according to Formula I as a soluble salt (acid addition salt or base salt) dissolved i.n a pharmaceutically acceptable liquid carrier such as, for example, water-for-injection and a buffer to provide a suitably buffered isotonic solution, for example, having a pH of about 3-7. Suitable buffering agents include, for example, trisodium orthophosphate, sodium bicarbonate, sodium citrate, N-methylglucamine, L(+)-lysine and L(+)-arginine to name but a few representative buffering agents.
The compound according to Formula I generally will be dissolved in the carrier in an amount sufficient to provide a pharmaceutically acceptable injectable concentration in the range of about 1 mg/ml to about 400 mg/ml of solution. The resulting liquid pharmaceutical composition will be administered so as to obtain the above-mentioned antibacterially effective amount of dosage. The compounds of Formula I
according to this invention, due to their aqueous solubility, are advantageously administered orally in solid and liquid dosage forms.
Antimicrobial activity was tested in vivo using the Murine Assay procedure.
Groups of female mice (six mice of 18-20 grams each) were injected intraperitoneally with bacteria which were thawed just prior to use and suspended in brain heart infusion with 4% brewers yeast UC8213 (Staphylococcus aureus) or brain heart infusion (Streptococcus species). Antibiotic treatment at six dose levels per drug was administered one hour and five hours after infection by either oral intubation or subcutaneous ("subcut.") routes. Survival was observed daily for six days.
ED5o values based on mortality ratios were calculated using probit analysis. The subject ,.
. WO 95/14684 PCT/LTS94/10582 compounds were compared against a well-known antimicrobial (Vancomycin) as a control. The data are shown in Table 1.
i WO 95114684. ~ ~ t~ PCTlUS94/1o582 ' _7_ In Vivo Activity of Examples VANCOMYCIN EDso Example ED mg/kg mg/kg (subcut.) ROUTE
1 5/4 2 oral/subcut.
2 9/15 5 oral/subcut.
3 16/8 8 oral/subcut.
4 2/2 2 oral/subcut.
5 ?/5 5 oral/subcut.
6 2/2 2 oral/subcut.
7 >20/1 6 oral/subcut.
8 10/6 5 oral/subcut.
9 2/3 1 oral/subcut.
10 1/2 3 oral/subcut.
11 8/8 4 oral/subcut.
12 12/>20 5 oral/subcut 13 >20/>20 4 oral/subcut.
14 3 2 oral 16 4 2 oral 17 5/2 2/1 oral/subcut.
18 14/>20 10 oral/subcut.
20 6/4 6 oral/subcut.
21 8/13 3 oral/subcut.
22 >18/4 3 oral/subcut.
23 2/1 3 oral/subcut.
24 1 'y oral 25 8/15 6 oral/subcut.
' 26 6/3 2 oral/subcut.
27 6 5 oral 29 9 4 oral In Table 1 the compound structures of each of the Examples are shown in Table 2 as follows:
' L1' . WO 95/14684 . PCT/US94/10582 Example R, R2 Rs 1 C(O)-C H4-morpholinyl H F , 2 C(O)-3-pyridinyl H F
3 C(O)-3-pyridinyl F F r 4 C(O)-1-imidazolyl H F
5 C(O)-1-imidazolyl F F
6 C(O)OC H40CH H F
7 C(O)p-N(CH )2Ph H F
8 C(O)p-N(CH )2Ph F F
9 C(O)CH2N(CH )2 H F
10 C(O)CH N(CH )2 F F
11 C(O)(CH )2N(CH )2 H F
12 C(O)(CH2) N(CH )2 H F
13 C(O)CH2-4-methyl-1-piperazinyl H F
14 C(O)CH F F
18 14/>20 10 oral/subcut.
20 6/4 6 oral/subcut.
21 8/13 3 oral/subcut.
22 >18/4 3 oral/subcut.
23 2/1 3 oral/subcut.
24 1 'y oral 25 8/15 6 oral/subcut.
' 26 6/3 2 oral/subcut.
27 6 5 oral 29 9 4 oral In Table 1 the compound structures of each of the Examples are shown in Table 2 as follows:
' L1' . WO 95/14684 . PCT/US94/10582 Example R, R2 Rs 1 C(O)-C H4-morpholinyl H F , 2 C(O)-3-pyridinyl H F
3 C(O)-3-pyridinyl F F r 4 C(O)-1-imidazolyl H F
5 C(O)-1-imidazolyl F F
6 C(O)OC H40CH H F
7 C(O)p-N(CH )2Ph H F
8 C(O)p-N(CH )2Ph F F
9 C(O)CH2N(CH )2 H F
10 C(O)CH N(CH )2 F F
11 C(O)(CH )2N(CH )2 H F
12 C(O)(CH2) N(CH )2 H F
13 C(O)CH2-4-methyl-1-piperazinyl H F
14 C(O)CH F F
15 C(O)C2H4C(O)OH F F
16 C(O)C2H C(O)O-Na+ F F
17 C(O)C2H4C(O)OH H F
18 C(O)C2H4C(O)CH F F
19 C(O)C2H4C(O)CH H F
20 P(O)(OH)2 H F
21 C(O)p-NHZPh H F
22 C(O)C(CH )(CHZOH)2 H F
23 C(O)CH20H H F
24 C(O)CHZOH F F
25 C(O)CH20CH H F
r 26 C(O)CZH4-4-morpholinyl F F
r 26 C(O)CZH4-4-morpholinyl F F
27 C(O)CH -4-morpholinyl H F
28 C(O)p[NHC(O)CH2N(CH ) )Ph H F
29 C(O)p-NHC(O)CH2NH2 H F
30 C(O)CH3 H F
WO 95/14684 . PCT/fJS94/I0582 _9_ Example 1: 3-(4-Morpholinyl)propionic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-ogazolidinyl)-2-fluorophenyl)-1-piperazinyl)-2-osoethyl ester, (S) A 3 liter 3-neck flask fitted with a mechanical stirrer, thermometer and nitrogen inlet was charged with 45.789 g of (S)-N-[[3-fluoro-4-( 1-piperazinyl)phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide and 1.3 liters of CH2C1. The mixture was cooled in an ice bath and 38 ml of triethylamine was added under nitrogen, then 28 ml of benzyloxyacetyl chloride was added via an addition funnel over 35 minutes, and the ice bath removed. After 1.5 hours, 500 ml of water was added, the layers were separated, and the organic phase washed with 500 ml of water. The aqueous layers were extracted with methylene chloride and the combined organic layers dried and concentrated which caused the precipitation of product. This was collected, filtered and washed with methylene chloride to yield 57.48 g of pure (S)-N-[[3-fluoro-4-(4-(benzyloxyacetyl)-1-piperazinyl)phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide.
A 5 L flask was charged with 29.04 g of this product and 2 L of 33%
methylene chloride/methanol (v/v) and was evacuated and filled with nitrogen.
The 8.1 g of 10% palladium/carbon was added as a slurry in 50 ml of methylene chloride/methanol (1:2, v/v), and the flask evacuated and filled with nitrogen, then evacuated and filled with hydrogen via balloon. The reaction mixture was stirred over night, the flack evacuated and filled with nitrogen, and the mixture filtered over diatomaceous earth, and the filter pad washed with 33% methylene chloride/methanol (v/v) and concentrated to give a white solid. This solid was purified by column chromatography (silica gel packed in chloroform), and gradient eluted with 3-11% methanol/chloroform to give a white foamy solid. This solid was take up in 10% methanoUethyacetate, and concentrated to dryness several times to give an amorphous white solid, 20.448 g (86.5%) of (S)-N-[[[3-fluoro-4-(4-(hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide, mp 17 6-177 °C, (hereinafter, referred to as "Intermediate") The Intermediate, 421 mg ( 1.07 mmol) was dissolved in 21 mL of pyridine.
To this solution was added 13 mg of DMAP, 268 mg (2.14 mmol) of 3-morpholinepropionic acid and 411 mg (2.14 mmol) of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride. The reaction was allowed to stir at room temperature, under N2 for 15 hours. After this time, the reaction was complete and was concentrated in aacuo. The crude product was purified twice by silica gel chromatography (30 g of silica gel, eluted with 0.5-4% MeOH/CHC13).
fter concentration of pure fractions, 372 mg (65%) of the title compound was recovered as ,.
WO 95/14684 ~ ~ PCT1US94/10582 a glassy, white solid. mp: 87-90 °C. Aqueous solubility (pH 7, phosphate bufFer) was 36 mg/ml.
Example 2: Nicotinic acid, 2-[4-[4-[5-[(acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2-tluorophenyl)-1-piperazinyl)-2-oxoethyl ester, (S)-A mixture of 251 mg (0.637 mmol) of the Intermediate from Ex. 1, 258 mg (1.35 mmol) of 1-ethyl-3-(3-dimethylamino) propylcarbodiimide, 169 mg (1.37 mmol) nicotinic acid and a catalytic amount of 4-dimethylaminopyridine in 5.0 ml of pyridine was stirred for 24 hours at room temperature. After this time, the mixture was concentrated in vacuo and the obtained crude was taken up in methylene chloride and placed upon a 23.5 cm x 2.5 cm 40 - 63 a silica column. The column was eluted with ethylacetate, 5% methanol / ethylacetate, 10% methanol /
ethylacetate, and 20% methanol / ethylacetate (250 ml each). The appropriate fractions were pooled to provide 300 mg (94%) of the title compound as white foamy solid. The solid changed to a glassy oil at 80-85 °C then melted at 173-175 °C.
Aqueous solubility (pH 7, phosphate buffer) was 0.3 mg/ml but a salt version should have higher solubility.
Example 3: Nicotinic acid, 2-[4-[4-[5-[(acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2,6-ditluorophenyl)-1-piperazinyl)-2-oxoethyl ester, (S)-6 The subject compound was prepared from (S) N [[3-[3,5-difluoro-4-[4-(hydroxyacetyl)-1-piperazinyl)phenyl)-2-oxo-5-oxazolidinyl)methyl]acetamide (preparation described in Ex. 15) in 77% yield (mp = 213-214 °C) following the same procedure as for Example 2. Aqueous solubility (pH 7, phosphate buffer) was 0.05 mg/ml but salt version should have higher solubility.
Example 4: 1H-imidazole-1-carboxylic acid, 2-[4-[4-[5-[(acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2-tluorophenyl)-1-piperazinyl)-2-oxoethyl ester, (S)-A mixture of 246 mg (0.624 mmol) of the Intermediate from Ex. 1 and 304 mg (1.875 mmol) of carbonyl diimidazole in 10 ml of tetrahydrofuran was stirred over night. The resulting precipitate was filtered away from the solvent, washed and dried to provide 251 mg (82 % yield) of the subject compound; (mp = 188-189 °C).
Aqueous solubility (pH 7, phosphate buffer) was 1.4 mg/ml.
Example 5: 1H-imidazole-1-carboxylic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2,6-ditluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-The subject compound was prepared from (S) N [[3-[3,5-difluoro-4-[4 (hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide (preparation described in Ex. 15) in 82% yield (mp = 199-200°C) following the same procedure as for Example 4.
Example 6: Carbonic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester-2-methoxyethyl ester, (S) To a solution of 175 mg (0.444 mmol) of the Intermediate from Ex. 1 in 5.0 ml methylene chloride at 0 °C under nitrogen was added 0.25 ml ( 1.79 mmol) triethlyamine followed by 129 mg (0.931 mmol) 2-methoxyethyl chloroformate as a solution in 0.5 ml methylene chloride. The mixture was allowed to slowly warm to room temperature over night. After stirring over night, 5 ml of 1 N HCl was added and the resulting solvent layers were separated. The aqueous layer was extracted with methylene chloride (2 x 5 ml). The combined organic layers were washed with brine and dried (MgS04) then concentrated to an oil. The crude was placed upon a 24 cm x 2.5 cm 40 - 63 a silica column. The column was eluted with ethylacetate (300 ml), 5% methanol / ethylacetate, 10% methanol / ethylacetate, 15%
methanol /
ethylacetate, and 20% methanol / ethylacetate (250 ml each). The appropriate fractions were pooled to provide 170 mg (77% yield) of the subject compound as a foamy solid. Part of the solid was crystallized from boiling ethylacetate to provide 65 mg (65% recovery) of the subject compound as a crystalline solid (mp = 149-°C). Aqueous solubility (pH 7, phosphate buffer) was 2.9 mg/ml.
Example 7: 4-dimethylaminobenzoic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-ozazolidinyl]-2-tluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-A mixture of 251 mg (0.637 mmol) of the Intermediate from Ex. 1, 181 mg (0.944 mmol) of 1-ethyl-3-(3-dimethylamino) propylcarbodiimide, 181 mg ( 1.10 mmol) 4-dimethylaminobenzoic acid and a catalytic amount of 4-dimethylamino pyridine in 3.0 ml of pyridine was stirred over night at room temperature. After this time, another 151 mg (0.914 mmol) of 4-dimethylaminobenzoic acid was added and stirring continued over night. After this time another 89 mg (0.464 mmol) of 1-ethyl-3-(3-dimethylamino) propylcarbodiimide was added to the mixture. The mixture was stirred for 5 days at room temperature and then warmed in a 50 °C oil . WO 95/14684 PCT/ITS94/10582 bath for one hour. The incomplete reaction mixture was then concentrated in vacuo.
The obtained crude was taken up in methylene chloride and placed upon a 24 cm x 2.5 cm 40 - 63 a silica column. The column was eluted with ethylacetate (250 ml), 10% methanol / ethylacetate (500 ml), 15% methanol / ethylacetate (250 ml), and 20% methanol / ethylacetate (500 ml). The appropriate fractions were pooled to provide 95 mg (41%) of a white solid which was triturated in ethylacetate to provide 75 mg (32%) of the subject compound as a white solid (mp = 210-211 °C).
Aqueous solubility (pH 7, phosphate buffer) was 0.01 mg/ml but salt version should have higher solubility.
Example 8: 4-dimethylaminobenzoic acid, 2-[4-[4-[5-[(acetylamino)methyl)-2-oxo-3-oxazolidinyl]-2,8-ditluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-The subject compound was prepared from (S) N [[3-[3,5-difluoro-4-[4 (hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide (preparation described in Ex. 15) in 59 % yield (mp = 199-202 °C) following the procedure used for Example 7. Aqueous solubility (pH 7, phosphate buffer) was 0.01 mg/ml but salt version should have higher solubility.
Example 9: Glycine, N,N-dimethyl-, 2-[4-[4-[S-[(acetylamino)methyl]-2-oxo-oxazolidinyl]-2-tluorophenyl]-1-piperazanyl]-2-oxoethyl ester, (S)-The Intermediate from Ex. 1 (250mg, 0.634 mmol) was dissolved into 8 ml of dry pyridine and ethyl-3-(3-dimethylamino)propyl carbodiimide hydrochloride (243mg, 1.27mmo1), DMAP (l6mg, 0.127 mmol) and N,N-dimethylglycine (131mg, 1.27 mmol) was added. The mixture was stirred under N2 at ambient temperature for 18 hours. After this time the solvent was removed under reduced pressure to give a gummy residue. The residue was dissolved into CH2Cl2, washed with water and brine. The organic phase was separated and dried over anhydrous Na2S04.
The solution was filtered and concentrated to give a solid that was purified by recrystallization from CH2C12/Et20. Isolated 220 mg of the subject compound as a white solid. mp=158-159°C. Aqueous solubility (pH 7, phosphate buffer) was 150 mg/ml.
Example 10: Glycine, N,N-dimethyl-, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-S-oxazolidinyl]-2,6-ditluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-This material was prepared in the same manner as Example 9, but starting with (S) N [[3-[3,5-difluoro-4-[4-(hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-'s .: w y.
. WO 95/14684 PCTlUS94l10582 oxazolidinyl]methyl] acetamide (preparation described in Ex. 15), mp=171-172°C.
Aqueous solubility (pH 7, phosphate buffer) was 4.2 mg/ml.
Example 11: 3-(Dimethylamino)propanoic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-ogo-3-ozazolidinyl]-2-tluorophenyl]-1-piperazinyl]-2-osoethyl ester, (S)-Methyl 3-(dimethylamino)propionate (2.Og, 15.2 mmol) was hydrolyzed to the acid by treatment with aqueous NaOH ( 18.2 mmol, 1.0 N solution) at reflux for hours. The solution was cooled to 0°C via an ice-bath and treated with 1.0 N HCl ( 18.2 mmol). The solution was lyophilized to give a waxy solid that was used without any further purification.
The Intermediate from Ex. 1 (400mg, 1.02 mmol) was dissolved into 10 ml of dry pyridine and the solution was treated with 3-(dimethylamino)propanoic acid (crude material, 239mg, 2.04 mmol), ethyl-3-(3-dimethylamino)propyl carbodiimide hydrochloride (391mg, 2.04 mmol) and DMAP (25mg, 0.204 mmol). The mixture was stirred at ambient temperature under N2 for 2.5 days. After this time the reaction mixture was concentrated under reduced pressure to give a solid residue. The residue was slurried into CH2Cl2 followed by washing with water and brine. The clear organic phase was separated and dried over anhydrous Na2S04. The dried solution was filtered and concentrated to a gum that was purified by recrystallization from CH2C12/Et20. Isolated 296 mg of the desired product as a dull white solid. mp=136-137°C.
Ezample 12: 4~(Dimethylamino)butanoic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-ozo-3-ozazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-o$oethyl ester, (S)-The Intermediate from Ex. 1 (400mg, 1.01 mmol) was dissolved into 10 ml of dry pyridine and the solution was treated with 4-(dimethylamino)butyric acid hydrochloride (341mg, 2.03 mmol), ethyl-3-(3-dimethylamino)propyl carbodiimide (389mg, 2.03mmo1) and DMAP (248mg, 2.03 mmol). The mixture was stirred at ambient temperature under N2 for 40 hours. After this time the reaction mixture was concentrated under reduced pressure to give a gummy residue. The residue was dissolved into CH2C12 followed by washing with water and brine. The organic phase was separated and dried over anhydrous Na2S04. Filtered and concentrated to give a glassy residue that was purified by recrystallization from CH2C12/Et20.
Isolated 178mg o~ the desired product as a white solid. mp=69-71°C. A~~ueous solubility (p~I
. WO 95/14684 PCT/US94/10582 7, phosphate buffer) was '34.6 ~ng/ml. ' Ezample 13: (4-Methyl-1-piperazinyl)acetic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-ogo-3-oxazolidinyl]-2-tluorophenyl]-1-piperazinyl]-2a-ozoethyl ester, (S)-The Intermediate from Ex. 1 (400mg, 1.01 mmol) was dissolved into 12 ml of dry CH2C12 and the solution was cooled to 0°C via an ice-bath. Next dry pyridine (92mg, 1.16 mmol) was added followed by chloroacetyl chloride (131mg, 1.16 mmol) dropwise via syringe. After 30 minutes the mixture was heated to a gentle reflux for 1 hour. The reaction was cooled and poured into a separatory funnel along with additional CH2C12. The solution was washed with 1% aqueous HCl, water and brine., The organic phase was dried over anhydrous Na2S04. Filtered and concentrated to a foam that was purified by recrystallization from CH2C12/Et20.
Isolated 407mg of the intermediate chloroacetyl eater. mp=173-174°C.
This chloroacetyl ester intermediate (303mg, 0.643mmo1) was dissolved into 7 ml of dry CH3CN and the solution was cooled to 0°C via an ice-bath.
Next N
methylpiperazine (258mg, 2.57 mmol) was added and the mixture was stirred at 0°C
for 1 hour followed by warming to room temperature for 3 hours. After this time TLC showed starting material was consumed. The reaction mixture was poured into a separatory funnel along with CHZC12. The solution was washed with water and brine. The organic phase was dried over anhydrous Na2S04. Filtered and concentrated to a glassy residue that was purified by recrystallization from CH2C12/Et20. Isolated 198mg of the desired product as a white solid. mp=128-129°C. Aqueous solubility (pH 7, phosphate buffer) was 79.1 mg/ml.
Example 14: Acetic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-ogo-3 oxazolidinyl)-2,6-ditluorophenyl)-1-piperazinyl)-2-ozoethyl ester, (S) A solution of the trifluoroacetic acid salt of difluoropiperazine oxazolidinone (preparation in Ex. 15, below) (0.454 g, 0.969 mmol) and potassium carbonate (0.159 g, 2.27 mmol) in 3 ml of methylene chloride was cooled to 0°C under nitrogen atmosphere. Acetoxyacetyl chloride (0.125 ml, 1.16 mmol) was then added in a dropwise fashion over 3 min aid syringe. The solution was allowed to gradually warm to room temperature as it stirred for 48 hours. Residual starting material was present therefore more acetoxyacetyl chloride (0.1 ml, 0.93 mmol) was added and the reaction mixture was stirred for an additional 2.5 hrs. The reaction mixture was then filtered and evaporated to give 0.371 g of crude material which was . WO 95/14684 PCT/US94/10582 subsequently purified on a silica column (40-63 u, 2.5 x 24 cm, packed and eluted with 5% methanol/ethyl acetate, collected 15 ml fractions) to give 0.107 g (24%) of the desired material as a white solid, mp 193-195°C, along with 0.096 g (28%
recovery) of the difluoropiperazine oxazolidinone free base. Aqueous solubility (pH
7, phosphate buffer) was 1.6 mg/ml.
Example 15: Succinic acid, 2-(4-(4-(S-((acetylamino)metl~yl)-2-ozo-3-oxazolidinyl)-2,6-difluorophenyl)-1-piperazinyl)-2-ozoethyl m~noester, (S) Part 1 demonstrates the preparation steps for difluorointermediates of the invention.
Part 1: (a) 2,6-difluoro-4-nitrobenzene(trifluoromethane)sulfonate.
2,6-Difluoro-4-nitrophenol (31.55 g, 180.19 mmol) was combined with CH2C12 (300 mL) and pyridine (29.15 mL, 360.38 mmol). The resultant slurry was cooled to 0 °C in an ice bath and then treated dropwise with triflic anhydride (31.8 rnL, 189.2 mmol) over a period of 45 minutes. The reaction was allowed to stir at 0 "C
for two hours and then it was stored in the refrigerator (5 °C) overnight. The reaction was determined to be complete by TLC (15% EtOAc/hexane, W short wave). The reaction mixture was concentrated under reduced pressure, and then treated with both H20 (50 mL) and EtOAc (50 mL). This mixture was transferred to a separatory funnel with more EtOAc (100 mL) and washed with 1N HCl until the washings were acidic (2 x 100 mL). The aqueous phases were back-extracted with EtOAc (2 x 200 mL). The combined EtOAc extracts were combined and then washed again with 1N HCl (400 mL) and once with brine (400 mL). The organic phase was dried over anhydrous Na2S04, filtered and then concentrated to yield 54.092 g of a rec ~ld oil. Although the oil was pure by NMR, it was combined with crude products from two other runs and chromatographed over silica gel (550 g) packed with 5% EtOAc. Elution with 2 L each of -v% EtOAc and 10% EtOAc afforded a 95%
overall yield of the title compound as a pale yellow oil with HR,MS (M+) calcd for CqH2F5NOsS 306.9574, found 306.9590.
(b) 1-(tent-butoxycarbonyl)-4-(2.6-difluoro-4-nitrophenyl)piperazine.
A solution of 2,6-difluoro-4-~~fc,robenzene(trifluoromethane)sulfonate (55 g, mmol) in dry DMF (275 mL) was treated with 1-(tent-butoxycarbonyl)piperazine (45.71 g, 250 mmol). The resultant clear yellow solution turned orange upon the addition of N,N-diisopropylethylamine (47 mL, 269 mmol). The reaction was heated to reflux for 15 hours under N2. The reaction was determined to be complete by 4718.P CP
TLC (30% EtOAc/hexane, UV short wave). The reaction mixture was concentrated to dryness and combined with the crude product of another reaction for purification.
The crude material was dissolved in hot CH2C12 (420 mL; some solids unrelated to the product did not dissolve) and then chromatographed on three separate columns (2 columns with 750 g silica gel, packed with CH2C12, loaded with 180 mL
material, and eluted with 1 L each of 1-5% EtOAc/CH2C12; one column with 250 g silica gel, packed with CH2C12, loaded with 60 mL compound, and eluted with 2.5 and 5%
EtOAdCH2ClZ) to give an 8?% yield of the title compound as an orange solid with HR.MS (M+) calcd for ClbHisF2Ns04 343.1343, found 343.1358.
(c) 1-(tent-butoxycarbonyl)-4-[2,6-ditluoro-4-(benzyloxycarbonyl) aminophenyl]piperazine.
The 1-(tent-butoxycarbonyl)-4-(2,6-difluoro-4-nitrophenyl)piperazine (44.7 g, 130 mmol) was dissolved in 20% THF/MeOH (600 mL) in a 2 L flask. Ammonium formats (41 g, 651 mmol) was added portionwise, followed by 10% Pd-C ( 1.12 g, 2.5 weight %), with cooling in an ice bath. When the addition was completed the ice bath was removed. The flask became slightly warm, and the yellow color disappeared. The reaction was found to be complete by TLC (30% EtOAc/hexane, W short wave) in 1.5 hours. The reaction mixture was filtered through Celite"'~
(washing the filter cake with 500 mL MeOH). The filtrate was concentrated under reduced pressure to give a solid which was then treated with 1 L EtOAc and 500 mL
HzO. The layers were separated and then the organic layer was washed again with H20 (500 mL) and once with brine (500 mL). The aqueous portions were back-extracted with more EtOAc (2 x 300 mL). The combined organic extracts were dried over anhydrous NazS04, filtered and concentrated to yield a yellow solid (40.8 g) which was immediately dissolved in dry DMF (500 mL) and cooled to -20 °C
(icelMeOH bath) under N2. The solution was treated with N,N-dimethylaniline (20.6 mL, 163 mmol), followed by the dropwise addition of of benzyl chloroformate (21.5 mL, 143 mmol). The ice bath was allowed to dissipate overnight. The reaction was determined to be complete by TLC (30% EtOAc/hexane, W short wave). The mixture was concentrated down to a yellow oil, dissolved in 1 L of EtOAc, and washed with H20 (500 mL) and brine (500 mL). The aqueous portions were back-extracted with more EtOAc (2 x 300 mL). The combined organic extracts were dried over anhydrous NalSO~, filtered and concentrated to yield a yellow solid. The crude material was recrystallized from hot EtOAc/hexane to afford 39.11 g (67%) of the title compound as a pale yellow crystalline solid with mp 171-172 °C.
. WO 95/14684 ~ ~~ PCT/US94/10582 (d) [3-[3,5-difluoro-4-[4-(tent-butoxycarbonyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methanol.
The 1-(tent-butoxycarbonyl)-4-[2,6-difluoro-4-(benzyloxycarbonyl)aminophenyl]
piperazine (14.05 g, 31 mmol) was dissolved in dry THF (150 mL) and then cooled to -78 °C (dry ice/acetone). The reaction was next treated with with n-BuLi (21.6 mL, 35 mmol) dropwise over a 25 minute period. The reaction was allowed to stir at °C for 30 minutes and then (R)-(-)-glycidylbutyrate (4.89 mL, 35 mmol) was added dropwise over 7 minutes. The reaction was maintained at -78 °C for an additional minutes and then the bath was removed, allowing the reaction to slowly warm up 10 to room temperature overnight. The reaction was determined to be complete by TLC
(5% MeOH/CHC13, W short wave). The reaction mixture was diluted with 500 mL
CH2C12 and then washed with both H20 (3 x 300 mL) and brine (300 mL). The aqueous portions were back-extracted with more CH2C12 (3 x 400 mL). The combined organic extracts were dried over Na2S04, filtered and concentrated to give 15 a creamy yellow solid. The crude solid was purified by recrystallization from hot EtOAclhexane to give 11.063 g (85%) of the title compound as a white solid with mp 164-166 °C.
(e) [[3-[3,5-difluoro-4-[4-(tent-butoxycarbonyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl] p-toluenesulfonate.
The [3-[3,5-difluoro-4-[4-(tent-butoxycarbonyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methanol (24.2 g, 59 mmol) was dissolved in pyridine ( 110 mL) and then cooled to 0 °C (ice bath). Freshly recrystalized p-toluenesulfonyl chloride ( 13.4 g, 70 mmol) of was added and the reaction was allowed to stir at 0 °C
for 2.5 hours under N2. The flask was then stoppered and stored in the refrigerator (5 °C) overnight. The reaction mixture became a pale pink slurry. TLC revealed that some alcohol still remained. The reaction mixture was treated with additional p-toluenesulfonyl chloride (1.12 g, 5.85 mmol), catalytic 4-(dimethylamino) pyridine, and 20 mL of dry CH2C12 to facilitate stirring. After 4 hours at 0 °C, the reaction was found to be complete by TLC (5% MeOFi/CHZCIs, LTV short wave). The mixture was added to 750 mL ice water and the precipitated product isolated via suction filtration, washing it with both water ( 1 L) and ether (500 mL). After drying in vczcuo, 29.921 g (90%) of the title compound was obtained as white solid with mp 150.5-151.5 °C.
(f) [f3-[3,5-difluoro-4-[4-(tent-butoxycarbonyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]methanesulfonate.
The [3-[3,5-difluoro-4-[4-(tent-butoxycarbonyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methanol (3.831 g, 9.27 mmol) was dissolved in CH2C12 (40 mL), cooled to 0 °C, and treated with triethylamine ( 1.74 g, 2.4 mL, 17.22 mmol) under N2.
Methanesulfonyl chloride (1.48 g, 1 mL, 12.92 mmol) was slowly added over 1 min.
TLC analysis (20% acetone/CH2Cl2) after 0.5 h revealed the reaction to be complete.
The reaction mixture was diluted with CH2Cl2 (200 mL) and washed with water (3 x 50 mL) and brine (50 mL), dried over Na2S04, filtered and concentrated in vdcuo to furnish the title compound as an off white solid with HR,MS (M+) calcd for C~oH27F2N307S 491.1538, found 491.1543.
(g) [[3-[3,5-difluoro-4-[4-(tent-butoxycarbonyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]azide.
The [[3-[3,5-difluoro-4-[4-(tent-butoxycarbonyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl] p-toluenesulfonate (29.661 g, 52 mmol) was dissolved in dry DMF (125 mL) and then treated with solid NaN3 (10.19 g, 156 mmol) at room temperature. The reaction was heated to 60 °C for three hours and then allowed to cool to room temperature overnight under N2. The reaction was found to be complete by TLC (30% EtOAc/hexane, run twice, W short wave). The reaction mixture was concentrated in vacuo to give a cream colored solid. The crude product was dissolved in 600 mL EtOAc and then washed with both H20 (2 x 500 mL) and brine (500 mL). The aqueous portions were back-extracted with more EtOAc (2 x 400 mL). The combined organic extracts were dried over Na2S04, filtered and concentrated in vacuo to yield 22.41 g (91%) of the title compound as a pale yellow solid with mp 115-117 °C.
Employing essentially identical conditions, the corresponding mesylate was converted to the same azide.
(h) N-[[3-[3,5-difluoro-4-[4-(tent-butoxycarbonyl)-1-piperazinyl]phenyl]-2-oxo-oxazolidinyl]methyl)acetamide.
The [[3-[3,5-difluoro-4-[4-(tent-butoxycarbonyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]azide (22.4 g, 51 mmol) was dissolved in 1 L of EtOAc and then degassed three times with N2. Next, 10% Pd-C (4.48 g, 20% by weight) was added and the solution was degassed again three times (with N2) before replacing the atmosphere with H2 (balloon). After 3 hours, the reaction was determined to be WO 95114684 ~ PCT/US94110582 complete by TLC (20% MeOH/CHC13, W short wave). At this point, pyridine (8.26 mL, 102 mmol) was added, followed by treatment with acetic anhydride (9.64 mL, 102 mmol). The reaction mixture was allowed to stir overnight at room temperature. The reaction was found to be complete by TLC (20% MeOH/CHC13, UV short wave). The reaction mixture was filtered through celite (the filter cake was washed with 500 mL EtOAc), the filtrate concentrated down to approximately 600 mL, and washed with H20 (2 x 500 mL) and brine (500 mL). The aqueous portions were back-extracted with more EtOAc (2 x 500 mL). The combined organic extracts were dried over anhydrous Na2S04, filtered and concentrated to give a yellow solid. Recrystallization of the crude product from hot CHCls and hexane afforded 19.167 g (83%) of the difluoro title compound as a white solid with mp 177-179 °C.
Part 2: (S) N [[3,[3,5-difluoro-4-[4-(tent-butoxycarbonyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamid~e (7.1 g, 15.6 mmol) was dissolved in CH2C12 (20 mL) and then added to a cold solution of trifluoroacetic acid (24 mL). The reaction was allowed to stir at 0°C under N2 for 15 minutes, and then the ice bath was removed. After stirring at room temperature for 2 hours, the reaction was complete by TLC (10% MeOH/CHC13, UV short wave). The solvent was evaporated off in v~cuo t~ give a gummy brown solid. This solid was dissolved in 30% H20/acetone, and then treated with the portion wise addition of NaHC03 (7.87 g, 93.7 mmol). The reaction was stirred at room temperature for 20 minutes and then the trifluoroacetate salt was treated with benzyloxyacetyl chloride (3.70 mL, 23.4 mmol) added drop wise over 4 minutes. The reaction was allowed to stir overnight under N2 at room temperature. The reaction mixture was transferred to a separatory funnel with EtOAc (400 mL) and then washed with water ( 3 x 250 mL), saturated NaHC03 (250 mL), and brine (250 mL). The aqueous portions were back-extracted with both EtOAc and CH2Cl2. The organic layers were dried over anhydrous NaS04, filtered and concentrated to yield a yellow solid. The solid was adsorbed on silica gel (25 g) and then chromatographed (200 g SG), eluting with a gradient of 1-4% MeOH in 10% CHgCN/CHC13 to give 5.85 g (75%) of (S) N [[3-[3,5-difluoro-4-[4-(benzyloxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide as a white solid with a melting point of 172-173 °C.
Next, (S) N [[3-[3,5-difluoro-4-[4-(benzyloxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide (3.84 g, 7.6 mmol) was dissolved in hot 10%
EtOAc/MeOH ( 150 mL). After degassing the solution three times with N2, the Pearlman's catalyst (384 mg, 10% by weight) was added. The solution was degassed - ~ ---.-WO 95/14684 , PCT/US94/10582 again and then the atmosphere was replaced with H2. The reaction was stirred at room temperature for 4.5 hours. At this point, the reaction was found to be complete by TLC (10% MeOH/CHC13, ITV short wave). The solution was filtered through celite, washing the cake with EtOAc (250 mL). The filtrate was concentrated under reduced pressure to give a white solid. The material was chromatographed on silica gel (150 g), eluting with a gradient of 1-6, 10%
MeOH in 10% CH3CN/CHC13 to yield 3.078 g (98%) of (S) N [(3-[3,5-difluoro-4-[4-(hydroxyacetyl)-1-piperazi.nyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide as a white solid with a melting point of 160.5-162.5 °C.
The prepared product (0.247 g, 0.599 mmol), succinic anhydride (0.092 g, 0.919 mmol) and 4-dimethylaminopyridine (0.024 g, 0.196 mmol) were weighed into a flame dried flask. Pyridine (10 ml) was added and the solution was placed under nitrogen atmosphere. After stirring 24 hrs the reaction was not complete, therefore more succinic anhydride (0.096 g, 0.959 mmol) was added. The reaction mixture was stirred an additional 2 hours at room temperature then was heated at reflux for 35 min. The solvent was then removed via bulb to bulb distillation to give the crude product as a gummy oil. Water (35 ml) and methylene chloride (65 ml) were then added to the crude product, the phases were separated and the organic portion was extracted with sat. sodium bicarbonate (35 ml). This aqueous portion was then acidified with 3 M hydrochloric acid and was extracted with ethyl acetate 3 x 35 ml.
These organic portions were combined, dried with MgS04, and evaporated to give the desired product which was still slightly contaminated with succinic acid as a white solid (0.169 g). Because of the low recovery the aqueous portion was basified with sat. sodium bicarbonate and extracted with methylene chloride (30 ml).
The aqueous portion was again acidified with 3 M hydrochloric acid and was extracted with ethyl acetate (3 x 35 ml). The organics were then evaporated to give 0.161 g of white solid which contained the desired product and acetic and succinic acids.
The first batch of product was purified by recrystallization from methanol to give 0.120 g (39%) of white solid mp 143-144°C. The second batch was purified first by column chromatography (silica, 40 x 63 ~Z, 2 ml pipette, packed with 5%
methanol/ethyl acetate, eluted with ethyl acetate, 5% and 20% methanol/ethyl acetate, collected 2 ml fractions) then by recrystallization from methanol and chloroform to give an additional 0.078 g (25%) of the desired material as a white solid. Aqueous solubility (pH 7, phosphate buffer) was 12.3 mg/ml.
Eyample 16: Succinic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-osazolidinyl)-2,6-difluorophenyl)-1-piperazinyl)-2-ogoethyl monoester, sodium salt (S) The product from Ex. 15 was dissolved in 1 ml of 0.14 M sodium bicarbonate and 5 ml of water. This solution was then frozen and lyophilized to give 0.032 g (41%) of the desired material as a white gum.
l~xample 17: Succinic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-o~cazolidinyl)-2,6-ditluorophenyl)-1-piperazinyl)-2-o~oethyl monoester, (S) A pyridine solution (5 ml) of the Intermediate from Ex. 1 (0.267 g, 0.677 mmol), succinic anhydride (0.075 g, 0.749 mmol), and 4-dimethylaminopyridine was stirred for 6 days under nitrogen atm~~sphere. The reaction was then worked up even though there was still starting oxazolidinone present as indicated by tlc. The pyridine was evaporated on the high vacuum, and the residue was taken up in ethyl acetate (15 ml) and sat. sodium bicarbonate (35 ml). The phases were separated, the aqueous portion was acidified to pH 1 with 3 M hydrochloric acid and was extracted with a+hyl acetate (5 x 15 ml). These extractions were combined, cried with MgS04 an;.. ::vaporated to give 0.135 g of light pink solid. Because of the low recovery, the aqueous portion was extracted with more ethyl acetate (5 x 15 ml).
These extracts were dried with MgS04 and evaporated to give 0.177 g of white solid.
The solids were combined and subjected to another aqueous workup in order to upgrade the material. Thus, the solids were dissolved in 10 ml of sat. sodium bicarbonate and 15 ml of ethyl acetate. The phases were separated and the aqueous portion was acidified with 3 M hydrochloric acid, which was then extracted with ethyl acetate (5 x 10 ml). The organic portion was dried with MgS04, and evaporated to give the desired product (0.130 g, 39%) as a white solid, mp 67-70°C.
Aqueous solubility (pH 7, phosphate buffer) was 28 mg/ml.
Ezample 18: 4-Ozo-valeric acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-ogazolidinyl)-2,6-ditluorophenyl)-1-piperazinyl)-2-ozoethyl ester, (S) (S) N [[3-[3,5-difluoro-4 ~ -'..-(hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamidepreparation described in Ex. 15) (0.178 g, 0.432 mmol), ethyl-3-(3-dimethylamino)propyl carbodiimide hydrochloride (0.161 g, 0.839 mmol), and 4-dimethylaminopyridine (0.007 g, 0.057 mmol) were weighed into a flame dried flask. Pyridine (3 ml) was added and the system was placed under nitrogen atmosphere, the levulinic acid (0.07 ml, 0.683 mmol) was added. After ' -22 stirring for 5 days the pyridine was evaporated on the high vacuum to give the crude material as a yellow oil. The quality of the crude material was upgraded on a small.
column, (silica, 40 x 63 u, 2 ml pipette, packed with ethyl acetate, eluted with methylene chloride, ethyl acetate, and 5% methanol/ethyl acetate, collected 1 ml fractions). The quality was further improved on a second column (mp, silica, 40 x 63 u, 1.5 x 27 cm, packed with ethyl acetate, eluted with ethyl acetate and 5%
methanol/ethyl acetate, collected 20 ml fractions) to give white solid which was still slightly contaminated. This solid was recrystallized from ethyl acetate to give 0.152 g (69%) of the desired material as a white solid, mp 130-133°C. Aqueous solubility (pH 7, phosphate buffer) was 1.2 mg/ml.
Example 18: 4-Oxo-valeric acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-ozazolidinyl)-2-tluorophenyl)-1-piperazinyl)-2-ozoethyl monoester, (S) The Intermediate from Ex. 1 (0.100 g, 0.253 mmol), ethyl-3-(3-dimethylamino)propyl carbodiimide hydrochloride (0.091 g, 0.475 mmol), and 4-dimethylaminopyridine (0.005 g, 0.041 mmol) were weighed into a flame dried flask.
Pyridine (3 ml) and levulinic acid (0.04 ml, 0.391 mmol) were added and the system was placed under nitrogen atmosphere. After stirring for 2 days the pyridine was evaporated under high vacuum and the resulting residue was purified on a silica column (40 x 63 u. 1.5 x 25 cm, packed with ethyl acetate, loaded with methylene chloride and methanol, eluted with ethyl acetate and 5% methanol/ethyl acetate, collected 15 ml fractions) to give 0.136 g of desired product which was then recrystallized from ethyl acetate to give 0.074 g (59%) of the desired material as a white solid, mp 135.5-138°C. Aqueous solubility (pH 7, phosphate buffer) was 2.29 26 mg/ml.
Ezample 20: Phosphoric acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-ozazolidinyl)-2-tluorophenyl)-1-piperazinyl)-2-ozoethyl ester, (S) A solution of the Intermediate from Ex. 1 (200mg, 0.51mmo1) in dry acetonitrile (20mL) was cooled under nitrogen and treated with 1H-tetrazole (Aldrich) with stirring. In a separate flask, dibenzyl N,N-diethylphosphoramidite (483mg, 1.52mmo1) was dissolved in 7mL of dry acetonitrile and was transferred via cannula to the reaction mixture with stirring for 20 hours. The flask was cooled in an ice bath for 30 minutes, and the mixture treated with m-chloroperoxybenzoic acid. After 5 minutes, the ice bath was removed and the mixture stirred for 1.5 hours after which the mixture was cooled to 0°C and treated with a solution of l5mg w0 95114684 PCT/ITS94/10582 of sodium sulfite in lOmL of pH 7 buffer. The mixture was diluted with methylene chloride and extracted with water and saturated sodium sulfite solution. The organic layer was dried (Na2S04) and concentrated in vacuo to afford a colorless oil.
This material was subjected to radial chromatography eluting with a methylene chloride-methanol system to afford 250mg (75%) of the intermediate, phosphoric acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2-fluorophenyl)-1-piperazinyl)-2-oxoethyl ester, dibenylester, (S), as a white rigid foam. TLC:
Rf--0.51 (20:1 Methylene chloride-methanol). Exact Mass: calc'd for C32H3sFN40sP:
655.2333. Found:655.2347.
Next, a solution of the prepared intermediate, above, (350mg, 0.54mmol) was dissolved in 5mL of methanol resulting in a clear, colorless solution with a small amount of undissolved amorphous solid material. The solution was treated with 100mg of 10% palladium on carbon and hydrogen gas at atmosphere pressure for hours. The mixture was filtered through celite washing the filter pad with methanol and concentrated in vacuo to afford a rigid foam. This material was dissolved in water, filtered and lyophilized to afford a white solid, mp 119-122°C.
Aqueous solubility (pH 7, phosphate buffer) was 25.7 mg/ml.
Ezample 21: 4-aminobenzoic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oso-3-oxazolidinyl]-2-tluorophenyl]-1-piperazinyl]-2-osoethyl ester, (S)-To a mixture of 956 mg (2.426 mmol) the Intermediate from Ex. 1 and 0.7 ml (5.03 mmol) triethylamine in 20 ml of methylene chloride was added 553 mg (2.980 mmol) of 4-nitrobenzoyl chloride as a solid all at once. The mixture was stirred for 21.5 hours at room temperature. After this time, 10 ml of 1 N HCl was added to the mixture and the layers were separated. The aqueous layer was extracted with methylene chloride (4 x 10 ml). The combined organic layers were washed with brine and dried (MgS04) and concentrated in vacuo. The obtained foamy solids were taker; up in methylene chloride and placed upon a 24 cm x 2.5 em 40 - 63 a silica column and eluted off with ethyl acetate (250 ml), 10% methanol / ethylacetate (250 ml), 20% methanol / ethylacetate (250 ml), and 10% methanol / methylene chloride (250 ml). The appropriate fractions were pooled to provide 1.082 g of 4-nitrobenzoic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl eater, (S)-; as a yellow solid in 82 % yield (mp= 222 -224 °C).
Next, 845 mg (1.555 mmol) of this product and 460 mg of 10% palladium on carbon was stirred in 100 ml of methanol/methylene chloride (1:1) under hydrogen (from a balloon) for 2 hours. The mixture was then filtered over diatomaceous earth and the filter pad washed with 70. ml of methanol/methylene chloride (1:1).
The filtrate was concentrated in vaczio to provide 765 mg (96 % crude yield) of foamy solids. A 550 mg portion of the solids was taken up in methylene chloride and placed upon a 9 cm x 2.5 cm 70 - 230 mesh silica column. The column was eluted with 500 ml of 10 % methanol/ethylacetate. Upon partial concentration of the combined fractions product was seen to precipitate. The precipitate was collected by vacuum filtration to provide 352 mg of a white solid. A second crop (29 mg) of this compound was obtained upon concentrating the filtrate. And concentration of the final filtrate provide 165 mg of the title compound as a glassy solid. In all 546 mg of the title compound was obtained from the column (99% recovery). The white solids became a glassy solid between 110°C and 115°C and a free flowing liquid at >
215°C. Aqueous solubility (pH 7, phosphate buffer) was 0.03 mg/ml, although the salt version should be higher.
E$ample 22: 2,2-bis(hydroxymethyl)propionic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oso-3-ozazolidinyl]-2-tluorophenyl]-1-piperazinyl]-2-osoethyl ester, (S)-A solution of 183mg(0.46mmo1) of the Intermediate of Ex. 1 and 146mg(0.46mmo1) of 2,2-bis(benzyloxymethyl)propionic acid in 5mL of pyridine was treated with 98mg(0.51mmo1) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide and 57mg(0.46mmol) of dimethylaminopyridine with stirring under nitrogen. After 72h, the solvent was evaporated in v~cuo to afford a yellow oil which was chromatographed over silica gel eluting with a methylene chloride-methanol system.
These procedures afforded 82mg(26%) of a white rigid foam.
TLC: Rf--0.59 (20:1 methylene chloride-methanol).
A solution of this product 160mg (0.23mmo1) of in 7mL of methanol was treated under nitrogen with 50mg of 10% palladium on carbon and hydrogen gas at atmospheric pressure. After 16h, the mixture was filtered through celite and concentrated in vdcuo to afford a colorless oil. This material was subjected to radial chromatography eluting with a methylene chloride-methanol system to afford 99mg (85%) of the desired product as a white rigid foam.
TLC: Rf--0.26 (20:1 methylene chloride-methanol.
Aqueous solubility (pH 7, phosphate buffer) was 13 mg/ml.
Example 23: Hydroxyacetic acid, 2-[4-[4-[S-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-tluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S) To a mixture of 200 mg (0.508 mmol) of U-100592 (Ex. 1), 149 mg ( 1.47 mmol, 0.205 mL), and 5 mL methylene chloride at 0 °C, benzyloxyacetylchloride was added dropwise. The reaction was allowed to warm slowly up to room temperature.
After stirring for 5 hours, 5 mL of 1 N HCl was added, and the resulting layers were separated. The aqueous layer was extracted with methylene chloride (3 x 5 mL).
The combined organic layers were washed with brine and dried (MgS04) then filtered and concentrated to a white solid. The crude was dissolved in a small amount of methylene chloride :.-~:cl methanol and was placed on a 22 cm x 2.5 cm 40-63 a silica column. The column was eluted with ethyl acetate, 2% methanol /
ethylacetate, 4% methanol / ethyl acetate, 6% methanol / ethyl acetate, 8%
methanol / ethyl acetate, and 10% methanol / ethyl acetate (250 mL each). The appropriate fractions were pooled to provide 120 mg (44%) of benzyloxyacetic acid, 2-[4-[-[5-(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl] 1-piperazinyl]-2-oxoethyl eater, (S)-; as a white solid (mp = 146-148 °C).
A mixture of this product 170 mg (0.314 mmol), 15 mL methanol, 3 mL
methylene chloride, and 100 mg 10% palladium catalyst. The reaction flask was evacuated with hydrogen 3 times and was allowed to stir under hydrogen overnight.
The reaction was filtered by vacuum filtration with filter aid to remove the palladium c~.talyst and was concentrated to provide 130 mg (93% yield) of the title compound (mp = 105-107 °C). Aqueous solubility (pH 7, phosphate buffer) was 4.2 mg/ml.
Example 24: Hydroxyacetic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2,6-difluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S) N [[3-[3,5-difluoro-4-[4-(hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide (preparation described in Ex. 15) was used to prepare benzyloxyacetic acid, 2-[4-[4-[5-[(acetylamino)methyl}-2-oxo-3-oxazolidinyl]-2,6-difluorophenyl)-1-piperazinyl)-2-oxoethyl ester, (S)-, in a 62% yield (mp =
°C) following the same procedure as for Example 23.
The subject compound was prepared from benzyloxyacetic acid, 2-[4-[4-[5-[(acetylamino)methyl}-2-oxo-3-oxazolidinyl]-2,6-difluorophenyl]-1-piperazinyl]-oxoethyl ester, (S)-; in a 76% yield (mp = 106-108 °C) following the same procedure as for Ex. 23.
WO 95/14684 , PCT/US94/10582 Example 25: Methoxyacetic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2-tluorophenyl)-1-piperazinyl)-2-oxoethyl ester, (S) The (S) N [[3-[3-fluoro-4-[4-(hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide (263 mg, 0.67 mmol) was slurried in dry CH2C12 (10 mL) and cooled to 0 °C in an ice bath. The solution became homogeneous after the addition of the pyridine (0.216 mL, 2.67 mmol). Next, the methoxyacetyl chloride (0.064 mL, 0.69 mmol) was added drop wise. The reaction was stirred at 0 °C for 30 minutes and then the ice bath was removed. After one hour, the reaction was found to be complete by TLC (10% MeOH/CHC13, W short wave). The reaction mixture was diluted With CH2Cl2 (100 mL) and then washed with 1N HCI/brine (50 mL
each), saturated NaHC03/brine (50 mL each), and brine (100 mL). Each aqueous portion was back-extracted with more CHZC12 (2 x 25 mL). The organic layers were combined, dried over anhydrous NaS04, filtered, and concentrated under reduced pressure to give an orange solid. This solid was chromatographed on silica gel (35 g), eluting with a gradient of 1-5% MeOH in 10% CHgCN/CHC13 to give an orange solid. The latter solid was recrystallized by dissolving it in a minimal amount of CH2C12/MeOH and then triturating with ether to yield 158 mg (51%) of the title compound as an ofd white solid with a melting point of 147-148 °C.
Aqueous solubility (pH 7, phosphate buffer) was 6.4 mg/ml.
Example 26: 3-(N-morpholinyl)propionic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2,6-ditluorophenyl)-1-piperazinyl)-2-oxoethyl ester, (S) (S) N [[3-[3,5-difluoro-4-[4-(hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide (preparation described in Ex. 15), 250 mg (0.607 mmol) was dissolved in 10 mL of pyridine. To this solution was added 13 mg of DMAP, 192 mg ( 1.21 mmol) of 3-(N-morpholinyl)propionic acid and 232 mg ( 1.21 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride. The reaction was allowed to stir at room temperature, under NZ for 15 hours. After this time, the reaction was complete and was concentrated in vacuo. The crude product was purified by silica gel chromatography (10 g of silica gel, eluted with 1-4%
MeOH/CHC13). The recovered product (367 mg) contained a small amount of urea byproduct. A 250 mg protion of this material was further purified by radial chromatography (eluted with 1-66% MeOH/CHCI~). After concentration, 210 mg of analytically pure product was recovered as a glassy, white solid. The title product (92%) was recovered as a glassy, white solid. mp: 139-142 °C.
FTIR(mull): cni 1 3450(br), 1754, 1665, 1514, 1450, 1247, 1120, 1032, 836.
Anal: Calc'd for C2SH33F2Ns07 ' v3 H20: C, 53.66; H, 6.02; N, 12.52. Found:
C, 53.66; H, 6.01; N, 12.55. Aqueous solubility (pH 7, phosphate buffer) was 8.2 mg/ml.
MS(EI): m/z(rel. int.) 553[M+](1), 478(7), 229(19), 158(17), 100(66), 56(53), 43(100). [a] _ -7° (c = 9.67, CHC13).
Example 27: (4-morpholinyl)acetic acid, 2-(4-(4-(6-((acetylamino)-methyl)-2-ozo-3-ozazolidinyl)-2-tluorophenyl)-1-piperazinyl)-2-oxoethyl ester, (S) A solution of 140mg (0.272mmo1) of U-103676 in 3mL of dry acetonitrile was treated with 52mg (0.598mmo1) of morpholine with stirring for 18 hours. The mixture was diluted with methylene chloride and extracted with water to afford an ofd white solid. This material was subjected to silica gel chromatography eluting with a methanol-methylene chloride system to afford 115mg (81%) of the desired product as a white solid. TLC: Rf--0.33 (20:1 Methylene chloride-methanol).
Exact Mass: calc'd for C24H32F'' N50?' 521.286. Found: 521.2288. A~ .~eous solubility (pH
7, phosphate buffer) was 55.3 mg/ml.
Example 28: 4-N-(N,N-dimethylglycinyl)aminobenzoic acid, 2-[4-[4-[5-[(acetylamino) methyl]-2-ogo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-ozoethyl ester, (S)-A mixture of 204 mg (0.398 mmol) of the title compound from Ex. 21, catalytic amount (<10 mg) of 4-dimethylamino pyridine (DMAP), 156 mg (0.814 mmol) of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide and 147 mg ( 1.05 mmol) of N,N-dimethylglycine in 2.5 ml of pyridine was stirred over night at room temperature. The mixture was then concentrated in uacuo. The obtained crude was treated with 5 ml saturated aqueous sodium bicarbonate and 20 ml of water and extracted with methylene chloride (4 x 20 ml). The combined organic layers were washed with brine, dried (MgS04~ and purified on a 23 cm x 2.5 cm, 40 - 63 a silica gel column eluting with 5% methanol / methylene chloride (1 L) to provide 175 mg (74%) of the desired product as foamy solids. Trituration with 10 % methanol l ethylacetate of foamy solids from a different lot provided white solids with mp = 180 - 182 °C. Aqueous solubility (pH 7, phosphate buffer) was 0.09 mg/ml, although the salt version should be higher.
L
. WO 95J14684 PCT/US94/10582 Ezample 28: 4-N-(glycinyl)aminobenzoic acid, 2-[4-[4-[5-[(acetylamino)-methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-Step 1: A mixture of 100 mg (0.195 mmol) of the title compound from Ex. 21, 243 mg (1.27 mmol) of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide and 269 mg (1.29 mmol) of N-CBZ-glycine in 4.0 ml of pyridine with a catalytic amount (<10 mg) of 4-dimethylamino pyridine (DMAP), was stirred over night at room temperature.
The mixture was then concentrated in vacuo and the obtained crude was purified on a 23 cm x 2.5 cm, 40 - 63 lz silica gel column eluting with a methanol :
methylene chloride gradient (500 ml 2.5% MeOH/CH2Cl2, 500 ml 5% MeOH/CH2C12, 500 ml 10% MeOH/CHZC12) to provide 135 mg (99%) of 4-N-(N-carbobenzyl- oxyglycinyl) aminobenzoic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (s)- as white solids. Analysis Calc.: C, 59.65; H, 5.29; N, 11.93. Found: C, 59.37; H, 5.35; N, 11.54.
Sten 2: A mixture of this product 275 mg (0.391 mmol) and 170 mg of 10%
palladium on carbon in 75 ml methanol and 55 ml of methylene chloride was stirred over night under hydrogen (balloon). The mixture was then filtered over diatomaceous earth and the filtrate concentrated in vacuo. The obtained solids were triturated with methanol in a warm water bath then the mixture was cooled and the solids were collected by vacuum filtration to provide 211 mg (95% yield) of the desired product as ofI' white solids (mp 240°C decomposition). Aqueous solubility (pH 7, phosphate buffer) was 9.8 mg/ml.
Example 30: Acetic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3 oxazolidinyl]-2-tluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-A mixture of 519 mg of the Intermediate from Ex. 1 in 2.5 ml acetic anhydride and 10 ml pyridine was stirred at room temperature for 2 hr. The mixture was concentrated in vacuo to a white solid, and this was purified on a 24.5 cm x 2.5 cm, 40 - 63 a silica gel column, eluting with 500 ml of 10% methanol/
ethylacetate and 400 ml 15% methanol/ethylacetate (25 ml fractions). The appropriate fractions were pooled and concentrated in vacuo to provide 540 mg (94%) of the title compound as a foamy white solid. The solid was triturated with 15 , ml of 10% methanol/ethylacetate and the solids were collected by vacuum filtration and dried in a vacuum oven to provide 436 mg (76%) of the title compound as a fine white powder (mp= 199 - 201°C).
WO 95/14684 . PCT/fJS94/I0582 _9_ Example 1: 3-(4-Morpholinyl)propionic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-ogazolidinyl)-2-fluorophenyl)-1-piperazinyl)-2-osoethyl ester, (S) A 3 liter 3-neck flask fitted with a mechanical stirrer, thermometer and nitrogen inlet was charged with 45.789 g of (S)-N-[[3-fluoro-4-( 1-piperazinyl)phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide and 1.3 liters of CH2C1. The mixture was cooled in an ice bath and 38 ml of triethylamine was added under nitrogen, then 28 ml of benzyloxyacetyl chloride was added via an addition funnel over 35 minutes, and the ice bath removed. After 1.5 hours, 500 ml of water was added, the layers were separated, and the organic phase washed with 500 ml of water. The aqueous layers were extracted with methylene chloride and the combined organic layers dried and concentrated which caused the precipitation of product. This was collected, filtered and washed with methylene chloride to yield 57.48 g of pure (S)-N-[[3-fluoro-4-(4-(benzyloxyacetyl)-1-piperazinyl)phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide.
A 5 L flask was charged with 29.04 g of this product and 2 L of 33%
methylene chloride/methanol (v/v) and was evacuated and filled with nitrogen.
The 8.1 g of 10% palladium/carbon was added as a slurry in 50 ml of methylene chloride/methanol (1:2, v/v), and the flask evacuated and filled with nitrogen, then evacuated and filled with hydrogen via balloon. The reaction mixture was stirred over night, the flack evacuated and filled with nitrogen, and the mixture filtered over diatomaceous earth, and the filter pad washed with 33% methylene chloride/methanol (v/v) and concentrated to give a white solid. This solid was purified by column chromatography (silica gel packed in chloroform), and gradient eluted with 3-11% methanol/chloroform to give a white foamy solid. This solid was take up in 10% methanoUethyacetate, and concentrated to dryness several times to give an amorphous white solid, 20.448 g (86.5%) of (S)-N-[[[3-fluoro-4-(4-(hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide, mp 17 6-177 °C, (hereinafter, referred to as "Intermediate") The Intermediate, 421 mg ( 1.07 mmol) was dissolved in 21 mL of pyridine.
To this solution was added 13 mg of DMAP, 268 mg (2.14 mmol) of 3-morpholinepropionic acid and 411 mg (2.14 mmol) of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride. The reaction was allowed to stir at room temperature, under N2 for 15 hours. After this time, the reaction was complete and was concentrated in aacuo. The crude product was purified twice by silica gel chromatography (30 g of silica gel, eluted with 0.5-4% MeOH/CHC13).
fter concentration of pure fractions, 372 mg (65%) of the title compound was recovered as ,.
WO 95/14684 ~ ~ PCT1US94/10582 a glassy, white solid. mp: 87-90 °C. Aqueous solubility (pH 7, phosphate bufFer) was 36 mg/ml.
Example 2: Nicotinic acid, 2-[4-[4-[5-[(acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2-tluorophenyl)-1-piperazinyl)-2-oxoethyl ester, (S)-A mixture of 251 mg (0.637 mmol) of the Intermediate from Ex. 1, 258 mg (1.35 mmol) of 1-ethyl-3-(3-dimethylamino) propylcarbodiimide, 169 mg (1.37 mmol) nicotinic acid and a catalytic amount of 4-dimethylaminopyridine in 5.0 ml of pyridine was stirred for 24 hours at room temperature. After this time, the mixture was concentrated in vacuo and the obtained crude was taken up in methylene chloride and placed upon a 23.5 cm x 2.5 cm 40 - 63 a silica column. The column was eluted with ethylacetate, 5% methanol / ethylacetate, 10% methanol /
ethylacetate, and 20% methanol / ethylacetate (250 ml each). The appropriate fractions were pooled to provide 300 mg (94%) of the title compound as white foamy solid. The solid changed to a glassy oil at 80-85 °C then melted at 173-175 °C.
Aqueous solubility (pH 7, phosphate buffer) was 0.3 mg/ml but a salt version should have higher solubility.
Example 3: Nicotinic acid, 2-[4-[4-[5-[(acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2,6-ditluorophenyl)-1-piperazinyl)-2-oxoethyl ester, (S)-6 The subject compound was prepared from (S) N [[3-[3,5-difluoro-4-[4-(hydroxyacetyl)-1-piperazinyl)phenyl)-2-oxo-5-oxazolidinyl)methyl]acetamide (preparation described in Ex. 15) in 77% yield (mp = 213-214 °C) following the same procedure as for Example 2. Aqueous solubility (pH 7, phosphate buffer) was 0.05 mg/ml but salt version should have higher solubility.
Example 4: 1H-imidazole-1-carboxylic acid, 2-[4-[4-[5-[(acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2-tluorophenyl)-1-piperazinyl)-2-oxoethyl ester, (S)-A mixture of 246 mg (0.624 mmol) of the Intermediate from Ex. 1 and 304 mg (1.875 mmol) of carbonyl diimidazole in 10 ml of tetrahydrofuran was stirred over night. The resulting precipitate was filtered away from the solvent, washed and dried to provide 251 mg (82 % yield) of the subject compound; (mp = 188-189 °C).
Aqueous solubility (pH 7, phosphate buffer) was 1.4 mg/ml.
Example 5: 1H-imidazole-1-carboxylic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2,6-ditluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-The subject compound was prepared from (S) N [[3-[3,5-difluoro-4-[4 (hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide (preparation described in Ex. 15) in 82% yield (mp = 199-200°C) following the same procedure as for Example 4.
Example 6: Carbonic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester-2-methoxyethyl ester, (S) To a solution of 175 mg (0.444 mmol) of the Intermediate from Ex. 1 in 5.0 ml methylene chloride at 0 °C under nitrogen was added 0.25 ml ( 1.79 mmol) triethlyamine followed by 129 mg (0.931 mmol) 2-methoxyethyl chloroformate as a solution in 0.5 ml methylene chloride. The mixture was allowed to slowly warm to room temperature over night. After stirring over night, 5 ml of 1 N HCl was added and the resulting solvent layers were separated. The aqueous layer was extracted with methylene chloride (2 x 5 ml). The combined organic layers were washed with brine and dried (MgS04) then concentrated to an oil. The crude was placed upon a 24 cm x 2.5 cm 40 - 63 a silica column. The column was eluted with ethylacetate (300 ml), 5% methanol / ethylacetate, 10% methanol / ethylacetate, 15%
methanol /
ethylacetate, and 20% methanol / ethylacetate (250 ml each). The appropriate fractions were pooled to provide 170 mg (77% yield) of the subject compound as a foamy solid. Part of the solid was crystallized from boiling ethylacetate to provide 65 mg (65% recovery) of the subject compound as a crystalline solid (mp = 149-°C). Aqueous solubility (pH 7, phosphate buffer) was 2.9 mg/ml.
Example 7: 4-dimethylaminobenzoic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-ozazolidinyl]-2-tluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-A mixture of 251 mg (0.637 mmol) of the Intermediate from Ex. 1, 181 mg (0.944 mmol) of 1-ethyl-3-(3-dimethylamino) propylcarbodiimide, 181 mg ( 1.10 mmol) 4-dimethylaminobenzoic acid and a catalytic amount of 4-dimethylamino pyridine in 3.0 ml of pyridine was stirred over night at room temperature. After this time, another 151 mg (0.914 mmol) of 4-dimethylaminobenzoic acid was added and stirring continued over night. After this time another 89 mg (0.464 mmol) of 1-ethyl-3-(3-dimethylamino) propylcarbodiimide was added to the mixture. The mixture was stirred for 5 days at room temperature and then warmed in a 50 °C oil . WO 95/14684 PCT/ITS94/10582 bath for one hour. The incomplete reaction mixture was then concentrated in vacuo.
The obtained crude was taken up in methylene chloride and placed upon a 24 cm x 2.5 cm 40 - 63 a silica column. The column was eluted with ethylacetate (250 ml), 10% methanol / ethylacetate (500 ml), 15% methanol / ethylacetate (250 ml), and 20% methanol / ethylacetate (500 ml). The appropriate fractions were pooled to provide 95 mg (41%) of a white solid which was triturated in ethylacetate to provide 75 mg (32%) of the subject compound as a white solid (mp = 210-211 °C).
Aqueous solubility (pH 7, phosphate buffer) was 0.01 mg/ml but salt version should have higher solubility.
Example 8: 4-dimethylaminobenzoic acid, 2-[4-[4-[5-[(acetylamino)methyl)-2-oxo-3-oxazolidinyl]-2,8-ditluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-The subject compound was prepared from (S) N [[3-[3,5-difluoro-4-[4 (hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide (preparation described in Ex. 15) in 59 % yield (mp = 199-202 °C) following the procedure used for Example 7. Aqueous solubility (pH 7, phosphate buffer) was 0.01 mg/ml but salt version should have higher solubility.
Example 9: Glycine, N,N-dimethyl-, 2-[4-[4-[S-[(acetylamino)methyl]-2-oxo-oxazolidinyl]-2-tluorophenyl]-1-piperazanyl]-2-oxoethyl ester, (S)-The Intermediate from Ex. 1 (250mg, 0.634 mmol) was dissolved into 8 ml of dry pyridine and ethyl-3-(3-dimethylamino)propyl carbodiimide hydrochloride (243mg, 1.27mmo1), DMAP (l6mg, 0.127 mmol) and N,N-dimethylglycine (131mg, 1.27 mmol) was added. The mixture was stirred under N2 at ambient temperature for 18 hours. After this time the solvent was removed under reduced pressure to give a gummy residue. The residue was dissolved into CH2Cl2, washed with water and brine. The organic phase was separated and dried over anhydrous Na2S04.
The solution was filtered and concentrated to give a solid that was purified by recrystallization from CH2C12/Et20. Isolated 220 mg of the subject compound as a white solid. mp=158-159°C. Aqueous solubility (pH 7, phosphate buffer) was 150 mg/ml.
Example 10: Glycine, N,N-dimethyl-, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-S-oxazolidinyl]-2,6-ditluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-This material was prepared in the same manner as Example 9, but starting with (S) N [[3-[3,5-difluoro-4-[4-(hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-'s .: w y.
. WO 95/14684 PCTlUS94l10582 oxazolidinyl]methyl] acetamide (preparation described in Ex. 15), mp=171-172°C.
Aqueous solubility (pH 7, phosphate buffer) was 4.2 mg/ml.
Example 11: 3-(Dimethylamino)propanoic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-ogo-3-ozazolidinyl]-2-tluorophenyl]-1-piperazinyl]-2-osoethyl ester, (S)-Methyl 3-(dimethylamino)propionate (2.Og, 15.2 mmol) was hydrolyzed to the acid by treatment with aqueous NaOH ( 18.2 mmol, 1.0 N solution) at reflux for hours. The solution was cooled to 0°C via an ice-bath and treated with 1.0 N HCl ( 18.2 mmol). The solution was lyophilized to give a waxy solid that was used without any further purification.
The Intermediate from Ex. 1 (400mg, 1.02 mmol) was dissolved into 10 ml of dry pyridine and the solution was treated with 3-(dimethylamino)propanoic acid (crude material, 239mg, 2.04 mmol), ethyl-3-(3-dimethylamino)propyl carbodiimide hydrochloride (391mg, 2.04 mmol) and DMAP (25mg, 0.204 mmol). The mixture was stirred at ambient temperature under N2 for 2.5 days. After this time the reaction mixture was concentrated under reduced pressure to give a solid residue. The residue was slurried into CH2Cl2 followed by washing with water and brine. The clear organic phase was separated and dried over anhydrous Na2S04. The dried solution was filtered and concentrated to a gum that was purified by recrystallization from CH2C12/Et20. Isolated 296 mg of the desired product as a dull white solid. mp=136-137°C.
Ezample 12: 4~(Dimethylamino)butanoic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-ozo-3-ozazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-o$oethyl ester, (S)-The Intermediate from Ex. 1 (400mg, 1.01 mmol) was dissolved into 10 ml of dry pyridine and the solution was treated with 4-(dimethylamino)butyric acid hydrochloride (341mg, 2.03 mmol), ethyl-3-(3-dimethylamino)propyl carbodiimide (389mg, 2.03mmo1) and DMAP (248mg, 2.03 mmol). The mixture was stirred at ambient temperature under N2 for 40 hours. After this time the reaction mixture was concentrated under reduced pressure to give a gummy residue. The residue was dissolved into CH2C12 followed by washing with water and brine. The organic phase was separated and dried over anhydrous Na2S04. Filtered and concentrated to give a glassy residue that was purified by recrystallization from CH2C12/Et20.
Isolated 178mg o~ the desired product as a white solid. mp=69-71°C. A~~ueous solubility (p~I
. WO 95/14684 PCT/US94/10582 7, phosphate buffer) was '34.6 ~ng/ml. ' Ezample 13: (4-Methyl-1-piperazinyl)acetic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-ogo-3-oxazolidinyl]-2-tluorophenyl]-1-piperazinyl]-2a-ozoethyl ester, (S)-The Intermediate from Ex. 1 (400mg, 1.01 mmol) was dissolved into 12 ml of dry CH2C12 and the solution was cooled to 0°C via an ice-bath. Next dry pyridine (92mg, 1.16 mmol) was added followed by chloroacetyl chloride (131mg, 1.16 mmol) dropwise via syringe. After 30 minutes the mixture was heated to a gentle reflux for 1 hour. The reaction was cooled and poured into a separatory funnel along with additional CH2C12. The solution was washed with 1% aqueous HCl, water and brine., The organic phase was dried over anhydrous Na2S04. Filtered and concentrated to a foam that was purified by recrystallization from CH2C12/Et20.
Isolated 407mg of the intermediate chloroacetyl eater. mp=173-174°C.
This chloroacetyl ester intermediate (303mg, 0.643mmo1) was dissolved into 7 ml of dry CH3CN and the solution was cooled to 0°C via an ice-bath.
Next N
methylpiperazine (258mg, 2.57 mmol) was added and the mixture was stirred at 0°C
for 1 hour followed by warming to room temperature for 3 hours. After this time TLC showed starting material was consumed. The reaction mixture was poured into a separatory funnel along with CHZC12. The solution was washed with water and brine. The organic phase was dried over anhydrous Na2S04. Filtered and concentrated to a glassy residue that was purified by recrystallization from CH2C12/Et20. Isolated 198mg of the desired product as a white solid. mp=128-129°C. Aqueous solubility (pH 7, phosphate buffer) was 79.1 mg/ml.
Example 14: Acetic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-ogo-3 oxazolidinyl)-2,6-ditluorophenyl)-1-piperazinyl)-2-ozoethyl ester, (S) A solution of the trifluoroacetic acid salt of difluoropiperazine oxazolidinone (preparation in Ex. 15, below) (0.454 g, 0.969 mmol) and potassium carbonate (0.159 g, 2.27 mmol) in 3 ml of methylene chloride was cooled to 0°C under nitrogen atmosphere. Acetoxyacetyl chloride (0.125 ml, 1.16 mmol) was then added in a dropwise fashion over 3 min aid syringe. The solution was allowed to gradually warm to room temperature as it stirred for 48 hours. Residual starting material was present therefore more acetoxyacetyl chloride (0.1 ml, 0.93 mmol) was added and the reaction mixture was stirred for an additional 2.5 hrs. The reaction mixture was then filtered and evaporated to give 0.371 g of crude material which was . WO 95/14684 PCT/US94/10582 subsequently purified on a silica column (40-63 u, 2.5 x 24 cm, packed and eluted with 5% methanol/ethyl acetate, collected 15 ml fractions) to give 0.107 g (24%) of the desired material as a white solid, mp 193-195°C, along with 0.096 g (28%
recovery) of the difluoropiperazine oxazolidinone free base. Aqueous solubility (pH
7, phosphate buffer) was 1.6 mg/ml.
Example 15: Succinic acid, 2-(4-(4-(S-((acetylamino)metl~yl)-2-ozo-3-oxazolidinyl)-2,6-difluorophenyl)-1-piperazinyl)-2-ozoethyl m~noester, (S) Part 1 demonstrates the preparation steps for difluorointermediates of the invention.
Part 1: (a) 2,6-difluoro-4-nitrobenzene(trifluoromethane)sulfonate.
2,6-Difluoro-4-nitrophenol (31.55 g, 180.19 mmol) was combined with CH2C12 (300 mL) and pyridine (29.15 mL, 360.38 mmol). The resultant slurry was cooled to 0 °C in an ice bath and then treated dropwise with triflic anhydride (31.8 rnL, 189.2 mmol) over a period of 45 minutes. The reaction was allowed to stir at 0 "C
for two hours and then it was stored in the refrigerator (5 °C) overnight. The reaction was determined to be complete by TLC (15% EtOAc/hexane, W short wave). The reaction mixture was concentrated under reduced pressure, and then treated with both H20 (50 mL) and EtOAc (50 mL). This mixture was transferred to a separatory funnel with more EtOAc (100 mL) and washed with 1N HCl until the washings were acidic (2 x 100 mL). The aqueous phases were back-extracted with EtOAc (2 x 200 mL). The combined EtOAc extracts were combined and then washed again with 1N HCl (400 mL) and once with brine (400 mL). The organic phase was dried over anhydrous Na2S04, filtered and then concentrated to yield 54.092 g of a rec ~ld oil. Although the oil was pure by NMR, it was combined with crude products from two other runs and chromatographed over silica gel (550 g) packed with 5% EtOAc. Elution with 2 L each of -v% EtOAc and 10% EtOAc afforded a 95%
overall yield of the title compound as a pale yellow oil with HR,MS (M+) calcd for CqH2F5NOsS 306.9574, found 306.9590.
(b) 1-(tent-butoxycarbonyl)-4-(2.6-difluoro-4-nitrophenyl)piperazine.
A solution of 2,6-difluoro-4-~~fc,robenzene(trifluoromethane)sulfonate (55 g, mmol) in dry DMF (275 mL) was treated with 1-(tent-butoxycarbonyl)piperazine (45.71 g, 250 mmol). The resultant clear yellow solution turned orange upon the addition of N,N-diisopropylethylamine (47 mL, 269 mmol). The reaction was heated to reflux for 15 hours under N2. The reaction was determined to be complete by 4718.P CP
TLC (30% EtOAc/hexane, UV short wave). The reaction mixture was concentrated to dryness and combined with the crude product of another reaction for purification.
The crude material was dissolved in hot CH2C12 (420 mL; some solids unrelated to the product did not dissolve) and then chromatographed on three separate columns (2 columns with 750 g silica gel, packed with CH2C12, loaded with 180 mL
material, and eluted with 1 L each of 1-5% EtOAc/CH2C12; one column with 250 g silica gel, packed with CH2C12, loaded with 60 mL compound, and eluted with 2.5 and 5%
EtOAdCH2ClZ) to give an 8?% yield of the title compound as an orange solid with HR.MS (M+) calcd for ClbHisF2Ns04 343.1343, found 343.1358.
(c) 1-(tent-butoxycarbonyl)-4-[2,6-ditluoro-4-(benzyloxycarbonyl) aminophenyl]piperazine.
The 1-(tent-butoxycarbonyl)-4-(2,6-difluoro-4-nitrophenyl)piperazine (44.7 g, 130 mmol) was dissolved in 20% THF/MeOH (600 mL) in a 2 L flask. Ammonium formats (41 g, 651 mmol) was added portionwise, followed by 10% Pd-C ( 1.12 g, 2.5 weight %), with cooling in an ice bath. When the addition was completed the ice bath was removed. The flask became slightly warm, and the yellow color disappeared. The reaction was found to be complete by TLC (30% EtOAc/hexane, W short wave) in 1.5 hours. The reaction mixture was filtered through Celite"'~
(washing the filter cake with 500 mL MeOH). The filtrate was concentrated under reduced pressure to give a solid which was then treated with 1 L EtOAc and 500 mL
HzO. The layers were separated and then the organic layer was washed again with H20 (500 mL) and once with brine (500 mL). The aqueous portions were back-extracted with more EtOAc (2 x 300 mL). The combined organic extracts were dried over anhydrous NazS04, filtered and concentrated to yield a yellow solid (40.8 g) which was immediately dissolved in dry DMF (500 mL) and cooled to -20 °C
(icelMeOH bath) under N2. The solution was treated with N,N-dimethylaniline (20.6 mL, 163 mmol), followed by the dropwise addition of of benzyl chloroformate (21.5 mL, 143 mmol). The ice bath was allowed to dissipate overnight. The reaction was determined to be complete by TLC (30% EtOAc/hexane, W short wave). The mixture was concentrated down to a yellow oil, dissolved in 1 L of EtOAc, and washed with H20 (500 mL) and brine (500 mL). The aqueous portions were back-extracted with more EtOAc (2 x 300 mL). The combined organic extracts were dried over anhydrous NalSO~, filtered and concentrated to yield a yellow solid. The crude material was recrystallized from hot EtOAc/hexane to afford 39.11 g (67%) of the title compound as a pale yellow crystalline solid with mp 171-172 °C.
. WO 95/14684 ~ ~~ PCT/US94/10582 (d) [3-[3,5-difluoro-4-[4-(tent-butoxycarbonyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methanol.
The 1-(tent-butoxycarbonyl)-4-[2,6-difluoro-4-(benzyloxycarbonyl)aminophenyl]
piperazine (14.05 g, 31 mmol) was dissolved in dry THF (150 mL) and then cooled to -78 °C (dry ice/acetone). The reaction was next treated with with n-BuLi (21.6 mL, 35 mmol) dropwise over a 25 minute period. The reaction was allowed to stir at °C for 30 minutes and then (R)-(-)-glycidylbutyrate (4.89 mL, 35 mmol) was added dropwise over 7 minutes. The reaction was maintained at -78 °C for an additional minutes and then the bath was removed, allowing the reaction to slowly warm up 10 to room temperature overnight. The reaction was determined to be complete by TLC
(5% MeOH/CHC13, W short wave). The reaction mixture was diluted with 500 mL
CH2C12 and then washed with both H20 (3 x 300 mL) and brine (300 mL). The aqueous portions were back-extracted with more CH2C12 (3 x 400 mL). The combined organic extracts were dried over Na2S04, filtered and concentrated to give 15 a creamy yellow solid. The crude solid was purified by recrystallization from hot EtOAclhexane to give 11.063 g (85%) of the title compound as a white solid with mp 164-166 °C.
(e) [[3-[3,5-difluoro-4-[4-(tent-butoxycarbonyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl] p-toluenesulfonate.
The [3-[3,5-difluoro-4-[4-(tent-butoxycarbonyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methanol (24.2 g, 59 mmol) was dissolved in pyridine ( 110 mL) and then cooled to 0 °C (ice bath). Freshly recrystalized p-toluenesulfonyl chloride ( 13.4 g, 70 mmol) of was added and the reaction was allowed to stir at 0 °C
for 2.5 hours under N2. The flask was then stoppered and stored in the refrigerator (5 °C) overnight. The reaction mixture became a pale pink slurry. TLC revealed that some alcohol still remained. The reaction mixture was treated with additional p-toluenesulfonyl chloride (1.12 g, 5.85 mmol), catalytic 4-(dimethylamino) pyridine, and 20 mL of dry CH2C12 to facilitate stirring. After 4 hours at 0 °C, the reaction was found to be complete by TLC (5% MeOFi/CHZCIs, LTV short wave). The mixture was added to 750 mL ice water and the precipitated product isolated via suction filtration, washing it with both water ( 1 L) and ether (500 mL). After drying in vczcuo, 29.921 g (90%) of the title compound was obtained as white solid with mp 150.5-151.5 °C.
(f) [f3-[3,5-difluoro-4-[4-(tent-butoxycarbonyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]methanesulfonate.
The [3-[3,5-difluoro-4-[4-(tent-butoxycarbonyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methanol (3.831 g, 9.27 mmol) was dissolved in CH2C12 (40 mL), cooled to 0 °C, and treated with triethylamine ( 1.74 g, 2.4 mL, 17.22 mmol) under N2.
Methanesulfonyl chloride (1.48 g, 1 mL, 12.92 mmol) was slowly added over 1 min.
TLC analysis (20% acetone/CH2Cl2) after 0.5 h revealed the reaction to be complete.
The reaction mixture was diluted with CH2Cl2 (200 mL) and washed with water (3 x 50 mL) and brine (50 mL), dried over Na2S04, filtered and concentrated in vdcuo to furnish the title compound as an off white solid with HR,MS (M+) calcd for C~oH27F2N307S 491.1538, found 491.1543.
(g) [[3-[3,5-difluoro-4-[4-(tent-butoxycarbonyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]azide.
The [[3-[3,5-difluoro-4-[4-(tent-butoxycarbonyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl] p-toluenesulfonate (29.661 g, 52 mmol) was dissolved in dry DMF (125 mL) and then treated with solid NaN3 (10.19 g, 156 mmol) at room temperature. The reaction was heated to 60 °C for three hours and then allowed to cool to room temperature overnight under N2. The reaction was found to be complete by TLC (30% EtOAc/hexane, run twice, W short wave). The reaction mixture was concentrated in vacuo to give a cream colored solid. The crude product was dissolved in 600 mL EtOAc and then washed with both H20 (2 x 500 mL) and brine (500 mL). The aqueous portions were back-extracted with more EtOAc (2 x 400 mL). The combined organic extracts were dried over Na2S04, filtered and concentrated in vacuo to yield 22.41 g (91%) of the title compound as a pale yellow solid with mp 115-117 °C.
Employing essentially identical conditions, the corresponding mesylate was converted to the same azide.
(h) N-[[3-[3,5-difluoro-4-[4-(tent-butoxycarbonyl)-1-piperazinyl]phenyl]-2-oxo-oxazolidinyl]methyl)acetamide.
The [[3-[3,5-difluoro-4-[4-(tent-butoxycarbonyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]azide (22.4 g, 51 mmol) was dissolved in 1 L of EtOAc and then degassed three times with N2. Next, 10% Pd-C (4.48 g, 20% by weight) was added and the solution was degassed again three times (with N2) before replacing the atmosphere with H2 (balloon). After 3 hours, the reaction was determined to be WO 95114684 ~ PCT/US94110582 complete by TLC (20% MeOH/CHC13, W short wave). At this point, pyridine (8.26 mL, 102 mmol) was added, followed by treatment with acetic anhydride (9.64 mL, 102 mmol). The reaction mixture was allowed to stir overnight at room temperature. The reaction was found to be complete by TLC (20% MeOH/CHC13, UV short wave). The reaction mixture was filtered through celite (the filter cake was washed with 500 mL EtOAc), the filtrate concentrated down to approximately 600 mL, and washed with H20 (2 x 500 mL) and brine (500 mL). The aqueous portions were back-extracted with more EtOAc (2 x 500 mL). The combined organic extracts were dried over anhydrous Na2S04, filtered and concentrated to give a yellow solid. Recrystallization of the crude product from hot CHCls and hexane afforded 19.167 g (83%) of the difluoro title compound as a white solid with mp 177-179 °C.
Part 2: (S) N [[3,[3,5-difluoro-4-[4-(tent-butoxycarbonyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamid~e (7.1 g, 15.6 mmol) was dissolved in CH2C12 (20 mL) and then added to a cold solution of trifluoroacetic acid (24 mL). The reaction was allowed to stir at 0°C under N2 for 15 minutes, and then the ice bath was removed. After stirring at room temperature for 2 hours, the reaction was complete by TLC (10% MeOH/CHC13, UV short wave). The solvent was evaporated off in v~cuo t~ give a gummy brown solid. This solid was dissolved in 30% H20/acetone, and then treated with the portion wise addition of NaHC03 (7.87 g, 93.7 mmol). The reaction was stirred at room temperature for 20 minutes and then the trifluoroacetate salt was treated with benzyloxyacetyl chloride (3.70 mL, 23.4 mmol) added drop wise over 4 minutes. The reaction was allowed to stir overnight under N2 at room temperature. The reaction mixture was transferred to a separatory funnel with EtOAc (400 mL) and then washed with water ( 3 x 250 mL), saturated NaHC03 (250 mL), and brine (250 mL). The aqueous portions were back-extracted with both EtOAc and CH2Cl2. The organic layers were dried over anhydrous NaS04, filtered and concentrated to yield a yellow solid. The solid was adsorbed on silica gel (25 g) and then chromatographed (200 g SG), eluting with a gradient of 1-4% MeOH in 10% CHgCN/CHC13 to give 5.85 g (75%) of (S) N [[3-[3,5-difluoro-4-[4-(benzyloxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide as a white solid with a melting point of 172-173 °C.
Next, (S) N [[3-[3,5-difluoro-4-[4-(benzyloxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide (3.84 g, 7.6 mmol) was dissolved in hot 10%
EtOAc/MeOH ( 150 mL). After degassing the solution three times with N2, the Pearlman's catalyst (384 mg, 10% by weight) was added. The solution was degassed - ~ ---.-WO 95/14684 , PCT/US94/10582 again and then the atmosphere was replaced with H2. The reaction was stirred at room temperature for 4.5 hours. At this point, the reaction was found to be complete by TLC (10% MeOH/CHC13, ITV short wave). The solution was filtered through celite, washing the cake with EtOAc (250 mL). The filtrate was concentrated under reduced pressure to give a white solid. The material was chromatographed on silica gel (150 g), eluting with a gradient of 1-6, 10%
MeOH in 10% CH3CN/CHC13 to yield 3.078 g (98%) of (S) N [(3-[3,5-difluoro-4-[4-(hydroxyacetyl)-1-piperazi.nyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide as a white solid with a melting point of 160.5-162.5 °C.
The prepared product (0.247 g, 0.599 mmol), succinic anhydride (0.092 g, 0.919 mmol) and 4-dimethylaminopyridine (0.024 g, 0.196 mmol) were weighed into a flame dried flask. Pyridine (10 ml) was added and the solution was placed under nitrogen atmosphere. After stirring 24 hrs the reaction was not complete, therefore more succinic anhydride (0.096 g, 0.959 mmol) was added. The reaction mixture was stirred an additional 2 hours at room temperature then was heated at reflux for 35 min. The solvent was then removed via bulb to bulb distillation to give the crude product as a gummy oil. Water (35 ml) and methylene chloride (65 ml) were then added to the crude product, the phases were separated and the organic portion was extracted with sat. sodium bicarbonate (35 ml). This aqueous portion was then acidified with 3 M hydrochloric acid and was extracted with ethyl acetate 3 x 35 ml.
These organic portions were combined, dried with MgS04, and evaporated to give the desired product which was still slightly contaminated with succinic acid as a white solid (0.169 g). Because of the low recovery the aqueous portion was basified with sat. sodium bicarbonate and extracted with methylene chloride (30 ml).
The aqueous portion was again acidified with 3 M hydrochloric acid and was extracted with ethyl acetate (3 x 35 ml). The organics were then evaporated to give 0.161 g of white solid which contained the desired product and acetic and succinic acids.
The first batch of product was purified by recrystallization from methanol to give 0.120 g (39%) of white solid mp 143-144°C. The second batch was purified first by column chromatography (silica, 40 x 63 ~Z, 2 ml pipette, packed with 5%
methanol/ethyl acetate, eluted with ethyl acetate, 5% and 20% methanol/ethyl acetate, collected 2 ml fractions) then by recrystallization from methanol and chloroform to give an additional 0.078 g (25%) of the desired material as a white solid. Aqueous solubility (pH 7, phosphate buffer) was 12.3 mg/ml.
Eyample 16: Succinic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-osazolidinyl)-2,6-difluorophenyl)-1-piperazinyl)-2-ogoethyl monoester, sodium salt (S) The product from Ex. 15 was dissolved in 1 ml of 0.14 M sodium bicarbonate and 5 ml of water. This solution was then frozen and lyophilized to give 0.032 g (41%) of the desired material as a white gum.
l~xample 17: Succinic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-o~cazolidinyl)-2,6-ditluorophenyl)-1-piperazinyl)-2-o~oethyl monoester, (S) A pyridine solution (5 ml) of the Intermediate from Ex. 1 (0.267 g, 0.677 mmol), succinic anhydride (0.075 g, 0.749 mmol), and 4-dimethylaminopyridine was stirred for 6 days under nitrogen atm~~sphere. The reaction was then worked up even though there was still starting oxazolidinone present as indicated by tlc. The pyridine was evaporated on the high vacuum, and the residue was taken up in ethyl acetate (15 ml) and sat. sodium bicarbonate (35 ml). The phases were separated, the aqueous portion was acidified to pH 1 with 3 M hydrochloric acid and was extracted with a+hyl acetate (5 x 15 ml). These extractions were combined, cried with MgS04 an;.. ::vaporated to give 0.135 g of light pink solid. Because of the low recovery, the aqueous portion was extracted with more ethyl acetate (5 x 15 ml).
These extracts were dried with MgS04 and evaporated to give 0.177 g of white solid.
The solids were combined and subjected to another aqueous workup in order to upgrade the material. Thus, the solids were dissolved in 10 ml of sat. sodium bicarbonate and 15 ml of ethyl acetate. The phases were separated and the aqueous portion was acidified with 3 M hydrochloric acid, which was then extracted with ethyl acetate (5 x 10 ml). The organic portion was dried with MgS04, and evaporated to give the desired product (0.130 g, 39%) as a white solid, mp 67-70°C.
Aqueous solubility (pH 7, phosphate buffer) was 28 mg/ml.
Ezample 18: 4-Ozo-valeric acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-ogazolidinyl)-2,6-ditluorophenyl)-1-piperazinyl)-2-ozoethyl ester, (S) (S) N [[3-[3,5-difluoro-4 ~ -'..-(hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamidepreparation described in Ex. 15) (0.178 g, 0.432 mmol), ethyl-3-(3-dimethylamino)propyl carbodiimide hydrochloride (0.161 g, 0.839 mmol), and 4-dimethylaminopyridine (0.007 g, 0.057 mmol) were weighed into a flame dried flask. Pyridine (3 ml) was added and the system was placed under nitrogen atmosphere, the levulinic acid (0.07 ml, 0.683 mmol) was added. After ' -22 stirring for 5 days the pyridine was evaporated on the high vacuum to give the crude material as a yellow oil. The quality of the crude material was upgraded on a small.
column, (silica, 40 x 63 u, 2 ml pipette, packed with ethyl acetate, eluted with methylene chloride, ethyl acetate, and 5% methanol/ethyl acetate, collected 1 ml fractions). The quality was further improved on a second column (mp, silica, 40 x 63 u, 1.5 x 27 cm, packed with ethyl acetate, eluted with ethyl acetate and 5%
methanol/ethyl acetate, collected 20 ml fractions) to give white solid which was still slightly contaminated. This solid was recrystallized from ethyl acetate to give 0.152 g (69%) of the desired material as a white solid, mp 130-133°C. Aqueous solubility (pH 7, phosphate buffer) was 1.2 mg/ml.
Example 18: 4-Oxo-valeric acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-ozazolidinyl)-2-tluorophenyl)-1-piperazinyl)-2-ozoethyl monoester, (S) The Intermediate from Ex. 1 (0.100 g, 0.253 mmol), ethyl-3-(3-dimethylamino)propyl carbodiimide hydrochloride (0.091 g, 0.475 mmol), and 4-dimethylaminopyridine (0.005 g, 0.041 mmol) were weighed into a flame dried flask.
Pyridine (3 ml) and levulinic acid (0.04 ml, 0.391 mmol) were added and the system was placed under nitrogen atmosphere. After stirring for 2 days the pyridine was evaporated under high vacuum and the resulting residue was purified on a silica column (40 x 63 u. 1.5 x 25 cm, packed with ethyl acetate, loaded with methylene chloride and methanol, eluted with ethyl acetate and 5% methanol/ethyl acetate, collected 15 ml fractions) to give 0.136 g of desired product which was then recrystallized from ethyl acetate to give 0.074 g (59%) of the desired material as a white solid, mp 135.5-138°C. Aqueous solubility (pH 7, phosphate buffer) was 2.29 26 mg/ml.
Ezample 20: Phosphoric acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-ozazolidinyl)-2-tluorophenyl)-1-piperazinyl)-2-ozoethyl ester, (S) A solution of the Intermediate from Ex. 1 (200mg, 0.51mmo1) in dry acetonitrile (20mL) was cooled under nitrogen and treated with 1H-tetrazole (Aldrich) with stirring. In a separate flask, dibenzyl N,N-diethylphosphoramidite (483mg, 1.52mmo1) was dissolved in 7mL of dry acetonitrile and was transferred via cannula to the reaction mixture with stirring for 20 hours. The flask was cooled in an ice bath for 30 minutes, and the mixture treated with m-chloroperoxybenzoic acid. After 5 minutes, the ice bath was removed and the mixture stirred for 1.5 hours after which the mixture was cooled to 0°C and treated with a solution of l5mg w0 95114684 PCT/ITS94/10582 of sodium sulfite in lOmL of pH 7 buffer. The mixture was diluted with methylene chloride and extracted with water and saturated sodium sulfite solution. The organic layer was dried (Na2S04) and concentrated in vacuo to afford a colorless oil.
This material was subjected to radial chromatography eluting with a methylene chloride-methanol system to afford 250mg (75%) of the intermediate, phosphoric acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2-fluorophenyl)-1-piperazinyl)-2-oxoethyl ester, dibenylester, (S), as a white rigid foam. TLC:
Rf--0.51 (20:1 Methylene chloride-methanol). Exact Mass: calc'd for C32H3sFN40sP:
655.2333. Found:655.2347.
Next, a solution of the prepared intermediate, above, (350mg, 0.54mmol) was dissolved in 5mL of methanol resulting in a clear, colorless solution with a small amount of undissolved amorphous solid material. The solution was treated with 100mg of 10% palladium on carbon and hydrogen gas at atmosphere pressure for hours. The mixture was filtered through celite washing the filter pad with methanol and concentrated in vacuo to afford a rigid foam. This material was dissolved in water, filtered and lyophilized to afford a white solid, mp 119-122°C.
Aqueous solubility (pH 7, phosphate buffer) was 25.7 mg/ml.
Ezample 21: 4-aminobenzoic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oso-3-oxazolidinyl]-2-tluorophenyl]-1-piperazinyl]-2-osoethyl ester, (S)-To a mixture of 956 mg (2.426 mmol) the Intermediate from Ex. 1 and 0.7 ml (5.03 mmol) triethylamine in 20 ml of methylene chloride was added 553 mg (2.980 mmol) of 4-nitrobenzoyl chloride as a solid all at once. The mixture was stirred for 21.5 hours at room temperature. After this time, 10 ml of 1 N HCl was added to the mixture and the layers were separated. The aqueous layer was extracted with methylene chloride (4 x 10 ml). The combined organic layers were washed with brine and dried (MgS04) and concentrated in vacuo. The obtained foamy solids were taker; up in methylene chloride and placed upon a 24 cm x 2.5 em 40 - 63 a silica column and eluted off with ethyl acetate (250 ml), 10% methanol / ethylacetate (250 ml), 20% methanol / ethylacetate (250 ml), and 10% methanol / methylene chloride (250 ml). The appropriate fractions were pooled to provide 1.082 g of 4-nitrobenzoic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl eater, (S)-; as a yellow solid in 82 % yield (mp= 222 -224 °C).
Next, 845 mg (1.555 mmol) of this product and 460 mg of 10% palladium on carbon was stirred in 100 ml of methanol/methylene chloride (1:1) under hydrogen (from a balloon) for 2 hours. The mixture was then filtered over diatomaceous earth and the filter pad washed with 70. ml of methanol/methylene chloride (1:1).
The filtrate was concentrated in vaczio to provide 765 mg (96 % crude yield) of foamy solids. A 550 mg portion of the solids was taken up in methylene chloride and placed upon a 9 cm x 2.5 cm 70 - 230 mesh silica column. The column was eluted with 500 ml of 10 % methanol/ethylacetate. Upon partial concentration of the combined fractions product was seen to precipitate. The precipitate was collected by vacuum filtration to provide 352 mg of a white solid. A second crop (29 mg) of this compound was obtained upon concentrating the filtrate. And concentration of the final filtrate provide 165 mg of the title compound as a glassy solid. In all 546 mg of the title compound was obtained from the column (99% recovery). The white solids became a glassy solid between 110°C and 115°C and a free flowing liquid at >
215°C. Aqueous solubility (pH 7, phosphate buffer) was 0.03 mg/ml, although the salt version should be higher.
E$ample 22: 2,2-bis(hydroxymethyl)propionic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oso-3-ozazolidinyl]-2-tluorophenyl]-1-piperazinyl]-2-osoethyl ester, (S)-A solution of 183mg(0.46mmo1) of the Intermediate of Ex. 1 and 146mg(0.46mmo1) of 2,2-bis(benzyloxymethyl)propionic acid in 5mL of pyridine was treated with 98mg(0.51mmo1) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide and 57mg(0.46mmol) of dimethylaminopyridine with stirring under nitrogen. After 72h, the solvent was evaporated in v~cuo to afford a yellow oil which was chromatographed over silica gel eluting with a methylene chloride-methanol system.
These procedures afforded 82mg(26%) of a white rigid foam.
TLC: Rf--0.59 (20:1 methylene chloride-methanol).
A solution of this product 160mg (0.23mmo1) of in 7mL of methanol was treated under nitrogen with 50mg of 10% palladium on carbon and hydrogen gas at atmospheric pressure. After 16h, the mixture was filtered through celite and concentrated in vdcuo to afford a colorless oil. This material was subjected to radial chromatography eluting with a methylene chloride-methanol system to afford 99mg (85%) of the desired product as a white rigid foam.
TLC: Rf--0.26 (20:1 methylene chloride-methanol.
Aqueous solubility (pH 7, phosphate buffer) was 13 mg/ml.
Example 23: Hydroxyacetic acid, 2-[4-[4-[S-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-tluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S) To a mixture of 200 mg (0.508 mmol) of U-100592 (Ex. 1), 149 mg ( 1.47 mmol, 0.205 mL), and 5 mL methylene chloride at 0 °C, benzyloxyacetylchloride was added dropwise. The reaction was allowed to warm slowly up to room temperature.
After stirring for 5 hours, 5 mL of 1 N HCl was added, and the resulting layers were separated. The aqueous layer was extracted with methylene chloride (3 x 5 mL).
The combined organic layers were washed with brine and dried (MgS04) then filtered and concentrated to a white solid. The crude was dissolved in a small amount of methylene chloride :.-~:cl methanol and was placed on a 22 cm x 2.5 cm 40-63 a silica column. The column was eluted with ethyl acetate, 2% methanol /
ethylacetate, 4% methanol / ethyl acetate, 6% methanol / ethyl acetate, 8%
methanol / ethyl acetate, and 10% methanol / ethyl acetate (250 mL each). The appropriate fractions were pooled to provide 120 mg (44%) of benzyloxyacetic acid, 2-[4-[-[5-(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl] 1-piperazinyl]-2-oxoethyl eater, (S)-; as a white solid (mp = 146-148 °C).
A mixture of this product 170 mg (0.314 mmol), 15 mL methanol, 3 mL
methylene chloride, and 100 mg 10% palladium catalyst. The reaction flask was evacuated with hydrogen 3 times and was allowed to stir under hydrogen overnight.
The reaction was filtered by vacuum filtration with filter aid to remove the palladium c~.talyst and was concentrated to provide 130 mg (93% yield) of the title compound (mp = 105-107 °C). Aqueous solubility (pH 7, phosphate buffer) was 4.2 mg/ml.
Example 24: Hydroxyacetic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2,6-difluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S) N [[3-[3,5-difluoro-4-[4-(hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide (preparation described in Ex. 15) was used to prepare benzyloxyacetic acid, 2-[4-[4-[5-[(acetylamino)methyl}-2-oxo-3-oxazolidinyl]-2,6-difluorophenyl)-1-piperazinyl)-2-oxoethyl ester, (S)-, in a 62% yield (mp =
°C) following the same procedure as for Example 23.
The subject compound was prepared from benzyloxyacetic acid, 2-[4-[4-[5-[(acetylamino)methyl}-2-oxo-3-oxazolidinyl]-2,6-difluorophenyl]-1-piperazinyl]-oxoethyl ester, (S)-; in a 76% yield (mp = 106-108 °C) following the same procedure as for Ex. 23.
WO 95/14684 , PCT/US94/10582 Example 25: Methoxyacetic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2-tluorophenyl)-1-piperazinyl)-2-oxoethyl ester, (S) The (S) N [[3-[3-fluoro-4-[4-(hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide (263 mg, 0.67 mmol) was slurried in dry CH2C12 (10 mL) and cooled to 0 °C in an ice bath. The solution became homogeneous after the addition of the pyridine (0.216 mL, 2.67 mmol). Next, the methoxyacetyl chloride (0.064 mL, 0.69 mmol) was added drop wise. The reaction was stirred at 0 °C for 30 minutes and then the ice bath was removed. After one hour, the reaction was found to be complete by TLC (10% MeOH/CHC13, W short wave). The reaction mixture was diluted With CH2Cl2 (100 mL) and then washed with 1N HCI/brine (50 mL
each), saturated NaHC03/brine (50 mL each), and brine (100 mL). Each aqueous portion was back-extracted with more CHZC12 (2 x 25 mL). The organic layers were combined, dried over anhydrous NaS04, filtered, and concentrated under reduced pressure to give an orange solid. This solid was chromatographed on silica gel (35 g), eluting with a gradient of 1-5% MeOH in 10% CHgCN/CHC13 to give an orange solid. The latter solid was recrystallized by dissolving it in a minimal amount of CH2C12/MeOH and then triturating with ether to yield 158 mg (51%) of the title compound as an ofd white solid with a melting point of 147-148 °C.
Aqueous solubility (pH 7, phosphate buffer) was 6.4 mg/ml.
Example 26: 3-(N-morpholinyl)propionic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2,6-ditluorophenyl)-1-piperazinyl)-2-oxoethyl ester, (S) (S) N [[3-[3,5-difluoro-4-[4-(hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide (preparation described in Ex. 15), 250 mg (0.607 mmol) was dissolved in 10 mL of pyridine. To this solution was added 13 mg of DMAP, 192 mg ( 1.21 mmol) of 3-(N-morpholinyl)propionic acid and 232 mg ( 1.21 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride. The reaction was allowed to stir at room temperature, under NZ for 15 hours. After this time, the reaction was complete and was concentrated in vacuo. The crude product was purified by silica gel chromatography (10 g of silica gel, eluted with 1-4%
MeOH/CHC13). The recovered product (367 mg) contained a small amount of urea byproduct. A 250 mg protion of this material was further purified by radial chromatography (eluted with 1-66% MeOH/CHCI~). After concentration, 210 mg of analytically pure product was recovered as a glassy, white solid. The title product (92%) was recovered as a glassy, white solid. mp: 139-142 °C.
FTIR(mull): cni 1 3450(br), 1754, 1665, 1514, 1450, 1247, 1120, 1032, 836.
Anal: Calc'd for C2SH33F2Ns07 ' v3 H20: C, 53.66; H, 6.02; N, 12.52. Found:
C, 53.66; H, 6.01; N, 12.55. Aqueous solubility (pH 7, phosphate buffer) was 8.2 mg/ml.
MS(EI): m/z(rel. int.) 553[M+](1), 478(7), 229(19), 158(17), 100(66), 56(53), 43(100). [a] _ -7° (c = 9.67, CHC13).
Example 27: (4-morpholinyl)acetic acid, 2-(4-(4-(6-((acetylamino)-methyl)-2-ozo-3-ozazolidinyl)-2-tluorophenyl)-1-piperazinyl)-2-oxoethyl ester, (S) A solution of 140mg (0.272mmo1) of U-103676 in 3mL of dry acetonitrile was treated with 52mg (0.598mmo1) of morpholine with stirring for 18 hours. The mixture was diluted with methylene chloride and extracted with water to afford an ofd white solid. This material was subjected to silica gel chromatography eluting with a methanol-methylene chloride system to afford 115mg (81%) of the desired product as a white solid. TLC: Rf--0.33 (20:1 Methylene chloride-methanol).
Exact Mass: calc'd for C24H32F'' N50?' 521.286. Found: 521.2288. A~ .~eous solubility (pH
7, phosphate buffer) was 55.3 mg/ml.
Example 28: 4-N-(N,N-dimethylglycinyl)aminobenzoic acid, 2-[4-[4-[5-[(acetylamino) methyl]-2-ogo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-ozoethyl ester, (S)-A mixture of 204 mg (0.398 mmol) of the title compound from Ex. 21, catalytic amount (<10 mg) of 4-dimethylamino pyridine (DMAP), 156 mg (0.814 mmol) of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide and 147 mg ( 1.05 mmol) of N,N-dimethylglycine in 2.5 ml of pyridine was stirred over night at room temperature. The mixture was then concentrated in uacuo. The obtained crude was treated with 5 ml saturated aqueous sodium bicarbonate and 20 ml of water and extracted with methylene chloride (4 x 20 ml). The combined organic layers were washed with brine, dried (MgS04~ and purified on a 23 cm x 2.5 cm, 40 - 63 a silica gel column eluting with 5% methanol / methylene chloride (1 L) to provide 175 mg (74%) of the desired product as foamy solids. Trituration with 10 % methanol l ethylacetate of foamy solids from a different lot provided white solids with mp = 180 - 182 °C. Aqueous solubility (pH 7, phosphate buffer) was 0.09 mg/ml, although the salt version should be higher.
L
. WO 95J14684 PCT/US94/10582 Ezample 28: 4-N-(glycinyl)aminobenzoic acid, 2-[4-[4-[5-[(acetylamino)-methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-Step 1: A mixture of 100 mg (0.195 mmol) of the title compound from Ex. 21, 243 mg (1.27 mmol) of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide and 269 mg (1.29 mmol) of N-CBZ-glycine in 4.0 ml of pyridine with a catalytic amount (<10 mg) of 4-dimethylamino pyridine (DMAP), was stirred over night at room temperature.
The mixture was then concentrated in vacuo and the obtained crude was purified on a 23 cm x 2.5 cm, 40 - 63 lz silica gel column eluting with a methanol :
methylene chloride gradient (500 ml 2.5% MeOH/CH2Cl2, 500 ml 5% MeOH/CH2C12, 500 ml 10% MeOH/CHZC12) to provide 135 mg (99%) of 4-N-(N-carbobenzyl- oxyglycinyl) aminobenzoic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (s)- as white solids. Analysis Calc.: C, 59.65; H, 5.29; N, 11.93. Found: C, 59.37; H, 5.35; N, 11.54.
Sten 2: A mixture of this product 275 mg (0.391 mmol) and 170 mg of 10%
palladium on carbon in 75 ml methanol and 55 ml of methylene chloride was stirred over night under hydrogen (balloon). The mixture was then filtered over diatomaceous earth and the filtrate concentrated in vacuo. The obtained solids were triturated with methanol in a warm water bath then the mixture was cooled and the solids were collected by vacuum filtration to provide 211 mg (95% yield) of the desired product as ofI' white solids (mp 240°C decomposition). Aqueous solubility (pH 7, phosphate buffer) was 9.8 mg/ml.
Example 30: Acetic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3 oxazolidinyl]-2-tluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-A mixture of 519 mg of the Intermediate from Ex. 1 in 2.5 ml acetic anhydride and 10 ml pyridine was stirred at room temperature for 2 hr. The mixture was concentrated in vacuo to a white solid, and this was purified on a 24.5 cm x 2.5 cm, 40 - 63 a silica gel column, eluting with 500 ml of 10% methanol/
ethylacetate and 400 ml 15% methanol/ethylacetate (25 ml fractions). The appropriate fractions were pooled and concentrated in vacuo to provide 540 mg (94%) of the title compound as a foamy white solid. The solid was triturated with 15 , ml of 10% methanol/ethylacetate and the solids were collected by vacuum filtration and dried in a vacuum oven to provide 436 mg (76%) of the title compound as a fine white powder (mp= 199 - 201°C).
Claims (10)
1. A compound of structural Formula I:
or pharmaceutically acceptable salts thereof wherein:
R is -C(O)-R1, -PO3~ or -P(O)(OH)2;
R1 is C1-6 alkyl, -N(R4)2, C1-6 alkyl-N(R4)2, -phenyl-N(R4)2, -phenyl-NHC(O)CH2NH2, -C2H4-morpholinyl, pyridinyl, C1-6 alkyl-OH, C1-6 alkyl-OCH3, C1-6alkyl C(O)CH3, -O-C1-6 alkyl-OCH3, C0-3 alkyl-piperazinyl (optionally substituted with C1-3 alkyl), imidazolyl, C1-6 alkyl-COOH, or -C(CH2OH)2CH3;
R2 and R3 are independently selected from hydrogen and F except at least one of R2 and R3 is F;
R4 is independently selected from hydrogen and C1-6 alkyl.
or pharmaceutically acceptable salts thereof wherein:
R is -C(O)-R1, -PO3~ or -P(O)(OH)2;
R1 is C1-6 alkyl, -N(R4)2, C1-6 alkyl-N(R4)2, -phenyl-N(R4)2, -phenyl-NHC(O)CH2NH2, -C2H4-morpholinyl, pyridinyl, C1-6 alkyl-OH, C1-6 alkyl-OCH3, C1-6alkyl C(O)CH3, -O-C1-6 alkyl-OCH3, C0-3 alkyl-piperazinyl (optionally substituted with C1-3 alkyl), imidazolyl, C1-6 alkyl-COOH, or -C(CH2OH)2CH3;
R2 and R3 are independently selected from hydrogen and F except at least one of R2 and R3 is F;
R4 is independently selected from hydrogen and C1-6 alkyl.
2. The compound of Claim 1 wherein R is -C(O)-R1.
3. The compound of Claim 2 wherein R1 is -CH3, -CH2N(CH3)2, -C2H4-morpholinyl or -CH2OH.
4. The compound of Claim 1 wherein R is -P(O)(OH)2.
5. The compound of Claim 1 wherein R is -PO3~.
6. The compound of Claim 1 wherein one of R2 and R3 is F and the other is hydrogen.
7. The compound of Claim 1 which is:
1) 3-(4-Morpholinyl)propionic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)2-fluorphenyl)-1-piperazinyl)-2-oxoethyl eater, (S);
2) Nicotinic acid, 2-(4-[4-[5-((acetylamino)methyl]-2-oxo-3-oxazolidinyl)-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-;
3) Nicotinic acid, 2-(4-[4-(5-((acetylamino)methyl]-2-oxo-3-oxazolidinyl)-2,6-difluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-;
4) 1H-imidazole-1-carboxylic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl)-2-oxoethyl ester, (S)-;
5) 1H-imidazole-1-carboxylic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2,6-difluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-;
6) Carbonic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester-2-methoxyethyl ester, (S);
7) 4-dimethylaminobenzoic acid, 2-[4-[4-[5-[(acetylamino)methyl)-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-;
8) 4-dimethylaminobenzoic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2,6-difluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-;
9) Glycine, N,N-dimethyl-, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-;
10) Glycine, N,N-dimethyl-, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2,6-difluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-;
11) 3-(Dimethylamino)propanoic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl eater, (S)-;
12) 4-(Dimethylamino)butanoic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-;
13) (4-Methyl-1-piperazinyl)acetic acid, 2-[4-[4-[5-[(acetylamino)methyl)-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-;
14) Acetic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2,6-difluorophenyl)-1-piperazinyl)-2-oxoethyl ester, (S);
15) Succinic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2,6-difluorophenyl)-1-piperazinyl)-2-oxoethyl monoester, (S);
16) Succinic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2,6-difluorophenyl)-1-piperazinyl)-2-oxoethyl monoester, sodium salt (S);
17) Succinic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2,6-difluorophenyl)-1-piperazinyl)-2-oxoethyl monoester, (S);~
18) 4-Oxo-valeric acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2,6-difluorophenyl)-1-piperazinyl)-2-oxoethyl ester, (S);
19) 4-Oxo-valeric acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2-fluorophenyl)-1-piperazinyl)-2-oxoethyl monoester, (S);
20) Phosphoric acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2-fluorophenyl)-1-piperazinyl)-2-oxoethyl eater, (S);
21) 4-aminobenzoic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-;
22) 2,2-bis(hydroxymethyl)propionic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-;
23) Hydroxyacetic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S);
24) Hydroxyacetic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2,6-difluorophenyl]-1-piperazinyl]-2-oxoethyl ester,(S)-;
25) Methoxyacetic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2-fluorophenyl)-1-piperazinyl)-2-oxoethyl ester, (S);
26) 3-(N-morpholinyl)propionic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2,6-difluorophenyl)-1-piperazinyl)-2-oxoethyl ester, (S);
27) 4-N-(glycinyl)aminobenzoic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl)-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-; or 28) Acetic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-.
1) 3-(4-Morpholinyl)propionic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)2-fluorphenyl)-1-piperazinyl)-2-oxoethyl eater, (S);
2) Nicotinic acid, 2-(4-[4-[5-((acetylamino)methyl]-2-oxo-3-oxazolidinyl)-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-;
3) Nicotinic acid, 2-(4-[4-(5-((acetylamino)methyl]-2-oxo-3-oxazolidinyl)-2,6-difluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-;
4) 1H-imidazole-1-carboxylic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl)-2-oxoethyl ester, (S)-;
5) 1H-imidazole-1-carboxylic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2,6-difluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-;
6) Carbonic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester-2-methoxyethyl ester, (S);
7) 4-dimethylaminobenzoic acid, 2-[4-[4-[5-[(acetylamino)methyl)-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-;
8) 4-dimethylaminobenzoic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2,6-difluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-;
9) Glycine, N,N-dimethyl-, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-;
10) Glycine, N,N-dimethyl-, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2,6-difluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-;
11) 3-(Dimethylamino)propanoic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl eater, (S)-;
12) 4-(Dimethylamino)butanoic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-;
13) (4-Methyl-1-piperazinyl)acetic acid, 2-[4-[4-[5-[(acetylamino)methyl)-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-;
14) Acetic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2,6-difluorophenyl)-1-piperazinyl)-2-oxoethyl ester, (S);
15) Succinic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2,6-difluorophenyl)-1-piperazinyl)-2-oxoethyl monoester, (S);
16) Succinic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2,6-difluorophenyl)-1-piperazinyl)-2-oxoethyl monoester, sodium salt (S);
17) Succinic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2,6-difluorophenyl)-1-piperazinyl)-2-oxoethyl monoester, (S);~
18) 4-Oxo-valeric acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2,6-difluorophenyl)-1-piperazinyl)-2-oxoethyl ester, (S);
19) 4-Oxo-valeric acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2-fluorophenyl)-1-piperazinyl)-2-oxoethyl monoester, (S);
20) Phosphoric acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2-fluorophenyl)-1-piperazinyl)-2-oxoethyl eater, (S);
21) 4-aminobenzoic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-;
22) 2,2-bis(hydroxymethyl)propionic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-;
23) Hydroxyacetic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S);
24) Hydroxyacetic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2,6-difluorophenyl]-1-piperazinyl]-2-oxoethyl ester,(S)-;
25) Methoxyacetic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2-fluorophenyl)-1-piperazinyl)-2-oxoethyl ester, (S);
26) 3-(N-morpholinyl)propionic acid, 2-(4-(4-(5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2,6-difluorophenyl)-1-piperazinyl)-2-oxoethyl ester, (S);
27) 4-N-(glycinyl)aminobenzoic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl)-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-; or 28) Acetic acid, 2-[4-[4-[5-[(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-.
8. Use of an amount of a compound of Formula I as defined in Claim 1 to treat microbial infections in warm blooded animals.
9. The use of Claim 8 wherein the amount of a compound of Formula I is about 0.1 to about 100 mg/kg of body weight/day.
10. The use of Claim 8 wherein the amount of a compound of Formula I is about 3.0 to about 50 mg/kg of body weight/day.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15598893A | 1993-11-22 | 1993-11-22 | |
| US155,988 | 1993-11-22 | ||
| PCT/US1994/010582 WO1995014684A1 (en) | 1993-11-22 | 1994-09-27 | Esters of substituted-hydroxyacetyl piperazine phenyl oxazolidinones |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2174107A1 CA2174107A1 (en) | 1995-06-01 |
| CA2174107C true CA2174107C (en) | 2005-04-12 |
Family
ID=22557606
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002174107A Expired - Fee Related CA2174107C (en) | 1993-11-22 | 1994-09-27 | Esters of substituted-hydroxyacetyl piperazine phenyl oxazolidinones |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US5652238A (en) |
| EP (1) | EP0730591B1 (en) |
| JP (1) | JP3698724B2 (en) |
| KR (1) | KR100312903B1 (en) |
| CN (1) | CN1046276C (en) |
| AT (1) | ATE182142T1 (en) |
| AU (1) | AU698699B2 (en) |
| CA (1) | CA2174107C (en) |
| CO (1) | CO4290433A1 (en) |
| DE (1) | DE69419523T2 (en) |
| DK (1) | DK0730591T3 (en) |
| ES (1) | ES2133588T3 (en) |
| GR (1) | GR3031420T3 (en) |
| IL (1) | IL111215A0 (en) |
| LV (1) | LV12538B (en) |
| NZ (1) | NZ274966A (en) |
| PE (1) | PE22896A1 (en) |
| TW (1) | TW427987B (en) |
| WO (1) | WO1995014684A1 (en) |
| ZA (1) | ZA947885B (en) |
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| GB9717804D0 (en) | 1997-08-22 | 1997-10-29 | Zeneca Ltd | Chemical compounds |
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| US4948801A (en) * | 1988-07-29 | 1990-08-14 | E. I. Du Pont De Nemours And Company | Aminomethyloxooxazolidinyl arylbenzene derivatives useful as antibacterial agents |
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-
1994
- 1994-09-27 AU AU80103/94A patent/AU698699B2/en not_active Ceased
- 1994-09-27 KR KR1019960702714A patent/KR100312903B1/en not_active IP Right Cessation
- 1994-09-27 DK DK94931278T patent/DK0730591T3/en active
- 1994-09-27 EP EP94931278A patent/EP0730591B1/en not_active Expired - Lifetime
- 1994-09-27 US US08/640,899 patent/US5652238A/en not_active Expired - Fee Related
- 1994-09-27 CA CA002174107A patent/CA2174107C/en not_active Expired - Fee Related
- 1994-09-27 CN CN94194241A patent/CN1046276C/en not_active Expired - Fee Related
- 1994-09-27 ES ES94931278T patent/ES2133588T3/en not_active Expired - Lifetime
- 1994-09-27 AT AT94931278T patent/ATE182142T1/en not_active IP Right Cessation
- 1994-09-27 NZ NZ274966A patent/NZ274966A/en unknown
- 1994-09-27 WO PCT/US1994/010582 patent/WO1995014684A1/en active IP Right Grant
- 1994-09-27 DE DE69419523T patent/DE69419523T2/en not_active Expired - Fee Related
- 1994-09-27 JP JP51504895A patent/JP3698724B2/en not_active Expired - Fee Related
- 1994-10-07 ZA ZA947885A patent/ZA947885B/en unknown
- 1994-10-10 IL IL11121594A patent/IL111215A0/en unknown
- 1994-10-13 TW TW083109509A patent/TW427987B/en not_active IP Right Cessation
- 1994-11-17 CO CO94052446A patent/CO4290433A1/en unknown
- 1994-11-17 PE PE1994254930A patent/PE22896A1/en not_active Application Discontinuation
-
1999
- 1999-10-07 GR GR990402509T patent/GR3031420T3/en unknown
-
2000
- 2000-07-14 LV LVP-00-91A patent/LV12538B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP0730591A1 (en) | 1996-09-11 |
| WO1995014684A1 (en) | 1995-06-01 |
| TW427987B (en) | 2001-04-01 |
| ES2133588T3 (en) | 1999-09-16 |
| NZ274966A (en) | 1998-01-26 |
| JPH09505582A (en) | 1997-06-03 |
| US5652238A (en) | 1997-07-29 |
| PE22896A1 (en) | 1996-06-07 |
| CO4290433A1 (en) | 1996-04-17 |
| GR3031420T3 (en) | 2000-01-31 |
| DE69419523D1 (en) | 1999-08-19 |
| CA2174107A1 (en) | 1995-06-01 |
| EP0730591B1 (en) | 1999-07-14 |
| ZA947885B (en) | 1996-04-09 |
| JP3698724B2 (en) | 2005-09-21 |
| IL111215A0 (en) | 1994-12-29 |
| AU8010394A (en) | 1995-06-13 |
| ATE182142T1 (en) | 1999-07-15 |
| CN1046276C (en) | 1999-11-10 |
| KR100312903B1 (en) | 2002-02-28 |
| LV12538B (en) | 2000-12-20 |
| AU698699B2 (en) | 1998-11-05 |
| CN1135752A (en) | 1996-11-13 |
| DE69419523T2 (en) | 1999-11-25 |
| DK0730591T3 (en) | 2000-01-31 |
| LV12538A (en) | 2000-10-20 |
| KR960705818A (en) | 1996-11-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| MKLA | Lapsed |