Background to the invention Antibiotic resistance is a serious concern globally as it would result in strains against which currently available antibacterial agents will be ineffective. In general, bacterial pathogens may be classified as either Gram-positive or Gram-negative pathogens.

Antibiotic compounds with effective activity against both Gram-positive and Gram- negative pathogens are generally regarded as having a broad spectrum of activity. The compounds of the present invention though being primarily effective against Gram- positive pathogens are also effective against certain Gram-negative pathogens.

Gram-positive pathogens, for example Staphylococci, Enterococci, Streptococci and Mycobacteria, are particularly important because of the development of resistant strains which are both difficult to treat and difficult to eradicate from the hospital environment once established. Examples of such strains are methicillin resistant staphylococcus (MRSA), methicillin resistant coagulase negative

staphylococci (MRCNS), penicillin resistant Streptococcus pneumoniae and multiply resistant Enterococcusfaecium and so on.

Antibacterial agents containing an oxazolidinone ring have been described in J. Med.

Chem. 1992,35, 2569-78 (Gregory W. A. et. al) and J Med. Chem. 1992,35, 1156-65 (Chung-Ho Park et. al). Also, US 4705799 and 5523403 and EP0316594 disclose substituted phenyl-2-oxazolidinones. US 4948801,5254577 & 5130316 discloses arylbenzene oxazolidinyl compounds including substituted or unsubstituted phenyl and pyridyl groups. Heteroaryl-oxazolidinones having one to three atoms selected from the group consisting of oxygen, sulfur, nitrogen and oxygen are described in EP 0697412, 0694544,0694543 & 0693491. Further, oxazolidinone derivatives useful as antibacterial agents are described in W00218354, W00218353, WO 0215980, WO 0220515, WO 0206278, WO 0181350, WO 0032599, WO 9807708, WO 9730981, WO 9721708, WO 9710235, WO 9709328, WO 9719089, WO 9710223, WO 9615130, WO 9613502, WO 9514684, WO 9507271, WO 9413649, W09323384, WO 9309103, WO 9002744, US 5700799, US 4801600, US 4921869, EP 0353781, EP 0316594, EP312000 etc.

Due to increase in antibiotic resistance there is a continuous need to develop more effective medicines suitable against such pathogenic organisms.

Summary of the invention The present invention describes a group of novel compounds useful as antibacterial agents. The novel compounds are defined by the general formula (I) below: The compounds of the present invention are useful in the treatment of the human or animal body, as preventives and therapeutics for infectious diseases. The compounds of this invention have excellent antimicrobial action against various human and veterinary pathogens including but not limited to multiply-resistant staphylococci and streptococci, as well as anaerobic organisms including those of the bacteroides and clostridia species, and acid-fast Mycobacterium tuberculosis and Mycobacterium avium with better efficacy, potency and minimum toxic effects.

Objects of the invention: The main objective of the present invention thus is to provide novel compounds of general formula (I), their analogs, their derivatives, their stereoisomers, their tautomeric forms, novel intermediates involved in their synthesis, their pharmaceutically acceptable salts, their pharmaceutically acceptable solvates and pharmaceutical compositions containing them or their mixtures suitable in the treatment of infectious diseases.

Another objective of the present invention is to provide a process for the preparation of novel compounds of general formula (I), their analogs, their derivatives, their stereoisomers, their polymorphs, their tautomeric forms, novel intermediates involved in their synthesis pharmaceutically acceptable salts, pharmaceutically acceptable solvates and pharmaceutical compositions containing them.

Yet another objective of the present invention is to provide pharmaceutical compositions containing compounds of general formula (I), their analogs, their derivatives, their stereoisomers, their polymorphs, their tautomeric forms, their pharmaceutically acceptable salts, solvates and their mixtures having pharmaceutically acceptable carriers, solvents, diluents, excipients and other media normally employed in their manufacture.

Still another objective of the present invention is to provide a method of treatment of antibiotic resistant pathogens, by administering a therapeutically effective amount of the compound of formula (I) or their pharmaceutically acceptable compositions to the mammals.

Detailed Description of the description The novel compounds of the present invention are defined by the general formula (I) below:

Where Ar represents an optionally substituted phenyl ring, five or six membered hetero aromatic ring which may be substituted or unsubstituted; Ri & Ra may be same or different and represent hydrogen, halogen, substituted or unsubstituted groups selected from alkyl, aralkyl, alkoxy, thio, amino, aminoalkyl, nitro, cyano, formyl, thioalkoxy, cycloalkyl, haloalkyl, haloalkoxy, groups; Y represents the groups Gl, G2 or G3 : where R3 & R4 may be same or different and represent H, Ci-C6 substituted or unsubstituted linear or branched alkyl group, halogen, hydroxy, cyano, haloalkyl, haloalkoxy, perhaloalkoxy, thio, substituted or unsubstituted groups selected from cycloalkyl, (Cl-Cl2) alkoxy, cyclo (C3-C7) alkoxy, aryl, aryloxy, aralkyl, ar (Cl-Cl2) alkoxy, acyl, acyloxy, carboxylic acid and its derivatives such as esters and amides, hydroxyalkyl, aminoalkyl, mono-substituted or di-substituted aminoalkyl, alkoxyalkyl, aryloxyalkyl, aralkoxyalkyl, (C1-C12)alkylthio, thio (Cl-Cl2) alkyl & arylthio X represents O, S or NRs where Rs represents H or (un) substituted alkyl or aryl groups; A represents a (un) substituted, saturated or unsaturated or partially saturated single or fused ring moiety, optionally containing one or more heteroatoms selected from N, S, O ; Z represents H, Cl-C6 substituted or unsubstituted alkyl group, cyano, haloalkyl, haloalkoxy, perhaloalkoxy, substituted or unsubstituted groups selected from cycloalkyl, bicycloalkyl, (Cl-C12) alkoxy, cyclo (C3-C7) alkoxy, aryl, aryloxy, aralkyl, ar (Cl- C12) alkoxy, heterocyclyl, heteroaryl, heterocyclyl (Cl-Cl2) alkyl, heteroar (Cl-C12) alkyl, heteroaryloxy, heteroar (Cl-Cl2) alkoxy, heterocycloxy, heterocyclylalkyloxy, acyl, acyloxy, acylamino, carboxylic acid and its derivatives such as esters and amides, hydroxyalkyl, aminoalkyl, mono-substituted or di-substituted aminoalkyl, alkoxyalkyl, aryloxyalkyl, aralkoxyalkyl, (Cl-Ci2) alkylthio, thio (Ci-Ci2) alkyl, arylthio, SOR6 and SO2R6, where R6 represents amino, optionally substituted groups selected from alkyl,

aryl, heteroaryl, heterocyclyl groups; the dotted line'------'represents either a bond or a no bond.

W represents OH, N3, NH2, NCS, OSO2CH3 O-heterocyclyloxy or a moiety of general formula Wherein R7 may be H, substituted or unsubstituted groups selected from amino, alkylamino, dialkylamino, aralkylamino, Cl-C6alkoxy, Cl-Cl2alkyl, aralkyl, C3- Cl2cycloalkyl, Cl-C6thioalkyl, Cl-C6haloalkyl, thioalkoxy, and X is selected from O, S, - NRs where Rs represents H, or substituted or unsubstituted alkyl group or aryl groups.

Suitable rings representing A may be selected from but are not limited to 5-6 membered ring systems which may be single or fused and examples of ring moieties in G, may be cyclohexanone, cyclopentanone, a-tetralone, indanone, 6-methoxy-a-tetralone, 5- methoxy tetralone, indole, 5-methoxy indanone, dihydrobenzothiophenone and the like.

Suitable substituents on groups A & Z may be selected from cyano, nitro, halo, perhaloalkyl, carboxyl, hydrazino, azido, formyl, amino, thio, hydroxy, sulfonyl, or substituted or unsubstituted groups selected from alkyl which may be linear or branched; cycloalkyl, alkenyl, cycloalkenyl, alkynyl, hydrazinoalkyl, alkylhydrazido, hydroxylamino, acyl, acyloxy, acylamino, carboxyalkyl, haloalkyl, aminoalkyl, haloalkoxy, hydroxyalkyl, alkoxyalkyl, thioalkyl, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylaminoalkyl, arylamino, alkylamino, aralkylamino, aralkoxy, haloaralkyl, alkenyl, aryl, aralkyl, aryloxy, alkoxy, alkylcarbonyl, alkoxycarbonyl, aryloxycarbonyl, aralkoxycarbonyl, alkylcarbonylalkyl, alkoxycarbonylalkyl, 1-alkoxycarbonyloxy-alkyl, 1-cycloalkyloxycarbonyloxy-alkyl, carboxamidoalkyl, cyanoamidino, cyanoalkyl, aminocarbonylalkyl, N-aminocarbonylalkyl, N-arylaminocarbonyl, N-alkyl-N- arylaminocarbonyl, carboxyalkylaminocarboxy, N-alkylamino, N, N-dialkylamino, N- arylamino, N-aralkylamino, N-alkyl-N-aralkylamino, N-alkyl-N-arylamino, N- alkylaminoalkyl, N, N-dialkylaminoalkyl, N-arylaminoalkyl, N-aralkylaminoalkyl, N- alkyl-N-aralkylaminoalkyl, N-aralkyl-N-alkylaminoalkyl, N-alkyl-N-arylaminoalkyl, N, N-dialkylaminocarbonyl, N-alkyl-N-arylaminocarbonyl, N-alkyl-N-

hydroxyaminocarbonyl, N-alkyl-N-hydroxyaminocarbonylalkyl, alkoxyalkyl, aryloxyalkyl, aralkoxyalkyl, arylthio, aralkylthio, alkoxycarbonyl, aminocarbonyl, alkoxycarbonylamino, cycloalkyl, bicycloalkyl, cycloalkoxy, bicycloalkenyl, heterocyclyl, heterocyclylalkyl, heteroaryl, heteroaralkyl, heteroaryloxy, heteroaralkoxy, heterocyclylalkyloxy, heterocycloalkoxycarbonyl, heteroaryloxycarbonyl, heteroaralkoxycarbonyl, RS02NH-and RSO2O-groups wherein R represents alkyl, aryl, heteroaryl, aralkyl, heteroaralkyl, heterocyclyl, heterocyclylalkyl groups.

The term"alkyl"used herein, either alone or in combination with other radicals, denotes a linear or branched radical containing one to twelve carbons, such as methyl, ethyl, n- propyl, iso-propyl, n-butyl, sec-butyl, tert-butyl, amyl, t-amyl, n-pentyl, n-hexyl, iso- hexyl, heptyl, octyl and the like.

The term"alkenyl"used herein, either alone or in combination with other radicals, denotes a linear or branched radical containing one to twelve carbons; such as vinyl, allyl, 2-butenyl, 3-butenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 2-hexenyl, 3-hexenyl, 4- hexenyl, 5-hexenyl, 2-heptenyl, 3-heptenyl, 4-heptenyl, 5-heptenyl, 6-heptenyl and the like. The term"alkenyl"includes dienes and trienes of straight and branched chains.

The term"alkynyl"used herein, either alone or in combination with other radicals, denotes a linear or branched radical containing one to twelve carbons, such as ethynyl, 1- propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-pentynyl, 2-pentynyl, 3- pentynyl, 4-pentynyl, 1-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, and the like. The term"alkynyl"includes di-and tri-ynes.

The term"cyclo (C3-C7) alkyl" used herein, either alone or in combination with other radicals, denotes a radical containing three to seven carbons, such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and the like.

The term"cyclo (C3-C7) alkenyl" used herein, either alone or in combination with other radicals, denotes a radical containing three to seven carbons, such as cyclopropenyl, 1- cyclobutenyl, 2-cylobutenyl, 1-cyclopentenyl, 2-cyclopentenyl, 3-cyclopentenyl, 1- cyclohexenyl, 2-cyclohexenyl, 3-cyclohexenyl, 1-cycloheptenyl, cycloheptadienyl, cycloheptatrienyl, and the like.

The term"alkoxy"used herein, either alone or in combination with other radicals, denotes a radical alkyl, as defined above, attached directly to an oxygen atom, such as methoxy, ethoxy, n-propoxy, iso-propoxy, n-butoxy, t-butoxy, iso-butoxy, pentyloxy, hexyloxy, and the like.

The term"alkenoxy"used herein, either alone or in combination with other radicals, denotes an alkenyl radical, as defined above, attached to an oxygen atom, such as vinyloxy, allyloxy, butenoxy, pentenoxy, hexenoxy, and the like.

The term"cyclo (C3-C7) alkoxy" used herein, either alone or in combination with other radicals, denotes a radical containing three to seven carbon atoms, such as cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, cyclohexyloxy, cycloheptyloxy and the like.

The term"halo"or"halogen"used herein, either alone or in combination with other radicals, such as"haloalkyl","perhaloalkyl"etc refers to a fluoro, chloro, bromo or iodo group. The term"haloallcyl"denotes a radical alkyl, as defined above, substituted with one or more halogens; such as perhaloalkyl, more preferably, perfluoro (Cl-C6) alkyl such as fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, difluoroethyl, trifluoroethyl, mono or polyhalo substituted methyl, ethyl, propyl, butyl, pentyl or hexyl groups. The term"haloalkoxy"denotes a haloalkyl, as defined above, directly attached to an oxygen atom, such as fluoromethoxy, chloromethoxy, fluoroethoxy chloroethoxy groups, and the like. The tenn"perhaloalkoxy"denotes a perhaloalkyl radical, as defined above, directly attached to an oxygen atom, trifluoromethoxy, trifluoroethoxy, and the like.

The term"aryl"or"aromatic"used herein, either alone or in combination with other radicals, denotes an aromatic system containing one, two or three rings wherein such rings may be attached together in a pendant manner or may be fused, such as phenyl, naphthyl, tetrahydronaphthyl, indane, biphenyl, and the like. The term'aralkyl"denotes an alkyl group, as defined above, attached to an aryl, such as benzyl, phenethyl, naphthylmethyl, and the like. The term"aryloxy"denotes an aryl radical, as defined above, attached to an alkoxy group, such as phenoxy, naphthyloxy and the like, which

may be substituted. The term"aralkoxy"denotes an arylalkyl moiety, as defined above, such as benzyloxy, phenethyloxy, naphthylmethyloxy, phenylpropyloxy, and the like, which may be substituted.

The term"heterocyclyl"or"heterocyclic"used herein, either alone or in combination with other radicals, denotes saturated, partially saturated and unsaturated ring-shaped radicals, the heteroatoms selected from nitrogen, sulfur and oxygen. Examples of saturated heterocyclic radicals include aziridinyl, azetidinyl, pyrrolidinyl, imidazolidinyl, piperidinyl, piperazinyl, 2-oxopiperidinyl, 4-oxopiperidinyl, 2-oxopiperazinyl, 3- oxopiperazinyl, morpholinyl, thiomorpholinyl, 2-oxomorpholinyl, azepinyl, diazepinyl, oxapinyl, thiazepinyl, oxazolidinyl, thiazolidinyl, and the like; examples of partially saturated heterocyclic radicals include dihydrothiophene, dihydropyran, dihydrofuran, dihydrothiazole, and the like.

The term"heteroaryl"or"heteroaromatic"used herein, either alone or in combination with other radicals, denotes unsaturated 5 to 6 membered heterocyclic radicals containing one or more hetero atoms selected from O, N or S, attached to an aryl group, such as pyridyl, thienyl, furyl, pyrrolyl, oxazolyl, thiazolyl, imidazolyl, isoxazolyl, oxadiazolyl, tetrazolyl, benzopyranyl, benzofuranyl, benzothienyl, indolinyl, indolyl, quinolinyl, pyrimidinyl, pyrazolyl, quinazolinyl, pyrimidonyl, benzoxazinyl, benzoxazinonyl, benzothiazinyl, benzothiazinonyl, benzoxazolyl, benzothizaolyl, benzimidazolyl, and the like.

The term"heterocyclyl (Ci-Cl2) alkyl" used herein, either alone or in combination with other radicals, represents a heterocyclyl group, as defined above, substituted with an alkyl group of one to twelve carbons, such as pyrrolidinealkyl, piperidinealkyl, morpholinealkyl, thiomorpholinealkyl, oxazolinealkyl, and the like, which may be substituted. The term"heteroaralkyl"used herein, either alone or in combination with other radicals, denotes a heteroaryl group, as defined above, attached to a straight or branched saturated carbon chain containing 1 to 6 carbons, such as (2-furyl) methyl, (3- furyl) methyl, (2-thienyl) methyl, (3-thienyl) methyl, (2-pyridyl) methyl, 1-methyl-1- (2- pyrimidyl) ethyl and the like. The terms"heteroaryloxy","heteroaralkoxy", "heterocycloxy", "heterocylylalkoxy"denotes heteroaryl, heteroarylalkyl, heterocyclyl, heterocylylalkyl groups respectively, as defined above, attached to an oxygen atom.

The term"acyl"used herein, either alone or in combination with other radicals, denotes a radical containing one to eight carbons such as formyl, acetyl, propanoyl, butanoyl, iso- butanoyl, pentanoyl, hexanoyl, heptanoyl, benzoyl and the like, which may be substituted.

The term"acyloxy"used herein, either alone or in combination with other radicals, denotes a radical acyl, as defined above, directly attached to an oxygen atom, such as acetyloxy, propionyloxy, butanoyloxy, iso-butanoyloxy, benzoyloxy and the like.

The term"acylamino"used herein, either alone or in combination with other radicals, denotes an acyl group as defined earlier, may be CH3CONH, C2H5CONH, C3H7CONH, C4H9CONH, C6H5CONH and the like, which may be substituted.

The term"mono-substituted amino"used herein, either alone or in combination with other radicals, denotes an amino group, substituted with one group selected from (Cl- C6) alkyl, substituted alkyl, aryl, substituted aryl or arylalkyl groups. Examples of monoalkylamino group include methylamine, ethylamine, n-propylamine, n-butylamine, n-pentylamine and the like.

The term'disubstituted amino"used herein, either alone or in combination with other radicals, denotes an amino group, substituted with two radicals that may be same or different selected from (Cl-C6) alkyl, substituted alkyl, aryl, substituted aryl, or arylalkyl groups, such as dimethylamino, methylethylamino, diethylamino, phenylmethyl amino and the like.

The term"arylamino"used herein, either alone or in combination with other radicals, denotes an aryl group, as defined above, linked through amino having a free valence bond from the nitrogen atom, such as phenylamino, naphthylamino, N-methyl anilino and the like.

The term"aralkylamino"used herein, either alone or in combination with other radicals, denotes an arylalkyl group as defined above linked through amino having a free valence

bond from the nitrogen atom e. g. benzylamino, phenethylamino, 3-phenylpropylamino, 1-napthylmethylamino, 2- (l-napthyl) ethylamino and the like.

The term"oxo"or"carbonyl"used herein, either alone (-C=O-) or in combination with other radicals, such as"alkylcarbonyl", denotes a carbonyl radical (-C=O-) substituted with an alkyl radical such as acyl or alkanoyl, as described above.

The term"carboxylic acid"used herein, alone or in combination with other radicals, denotes a-COOH group, and includes derivatives of carboxylic acid such as esters and amides. The term"ester"used herein, alone or in combination with other radicals, denotes-COO-group, and includes carboxylic acid derivatives, where the ester moieties are alkoxycarbonyl, such as methoxycarbonyl, ethoxycarbonyl, and the like, which may be substituted; aryloxycarbonyl group such as phenoxycarbonyl, napthyloxycarbonyl, and the like, which may be substituted; aralkoxycarbonyl group such as benzyloxycarbonyl, phenethyloxycarbonyl, napthylmethoxycarbonyl, and the like, which may be substituted; heteroaryloxycarbonyl, heteroaralkoxycarbonyl, wherein the heteroaryl group, is as defined above, which may be substituted; heterocyclyloxycarbonyl, where the heterocyclic group, as defined earlier, which may be substituted.

The term"amide"used herein, alone or in combination with other radicals, represents an aminocarbonyl radical (H2N-C=O-), wherein the amino group is mono-or di-substituted or unsubstituted, such as methylamide, dimethylamide, ethylamide, diethylamide, and the like. The term"aminocarbonyl"used herein, either alone or in combination with other radicals, with other terms such as'aminocarbonylalkyl","n-alkylaminocarbonyl", "N-arylaminocarbonyl","N, N-dialkylaminocarbonyl", "N-alkyl-N-arylaminocarbonyl", "N-alkyl-N-hydroxyaminocarbonyl", and"N-alkyl-N-hydroxyaminocarbonylalkyl", substituted or unsubstituted. The terms"N-alkylaminocabonyl"and"N, N- dialkylaminocarbonyl"denotes aminocarbonyl radicals, as defined above, which have been substituted with one alkyl radical and with two alkyl radicals, respectively.

Preferred are"lower alkylaminocarbonyl"having lower alkyl radicals as described above attached to aminocarbonyl radical. The terms"N-arylaminocarbonyl"and"N-alkyl-N- arylaminocarbonyl"denote amiocarbonyl radicals substituted, respectively, with one aryl

radical, or one alkyl, and one aryl radical. The term"aminocarbonylalkyl"includes alkyl radicals substituted with aminocarbonyl radicals.

The term"hydroxyalkyl"used herein, either alone or in combination with other radicals, denotes an alkyl group, as defined above, substituted with one or more hydroxy radicals, such as hydroxymethyl, hydroxyethyl, hydroxypropyl, hydroxybutyl, hydroxypentyl, hydroxyhexyl and the like.

The term"aminoalkyl"used herein, alone or in combination with other radicals, denotes an amino (-NH2) moiety attached to an alkyl radical, as defined above, which may be substituted, such as mono-and di-substituted aminoalkyl. The term"alkylamino"used herein, alone or in combination with other radicals, denotes an alkyl radical, as defined above, attached to an amino group, which may be substituted, such as mono-and di- substituted alkylamino.

The term"alkoxyalkyl"used herein, alone or in combination with other radicals, denotes an alkoxy group, as defined above, attached to an alkyl group, such as methoxymethyl, ethoxymethyl, methoxyethyl, ethoxyethyl and the like. The term"aryloxyalkyl"used herein, alone or in combination with other radicals, includes phenoxymethyl, napthyloxymethyl, and the like. The term"aralkoxyalkyl"used herein, alone or in combination with other radicals, includes C6H5CH2OCH2, C6HsCH20CH2CH2, and the like.

The term" (C1-C12) alkylthio" used herein, either alone or in combination with other radicals, denotes a straight or branched or cyclic monovalent substituent comprising an alkyl group of one to twelve carbon atoms, as defined above, linked through a divalent sulfur atom having a free valence bond from the sulfur atom, such as methylthio, ethylthio, propylthio, butylthio, pentylthio and the like. Examples of cyclic alkylthio are cyclopropylthio, cyclobutylthio, cyclopentylthio, cyclohexylthio and the like, which may be substituted.

The term"thio (C1-Cl2) alkyl" used herein, either alone or in combination with other radicals, denotes an alkyl group, as defined above, attached to a group of formula-SR',

where R'represents hydrogen, alkyl or aryl group, e. g. thiomethyl, methylthiomethyl, phenylthiomethyl and the like, which may be substituted.

The term"arylthio'used herein, either alone or in combination with other radicals, denotes an aryl group, as defined above, linked through a divalent sulfur atom, having a free valence bond from the sulfur atom such as phenylthio, napthylthio and the like.

The term" (C1-Cl2) alkoxycarbonylamino" used herein, alone or in combination with other radicals, denotes an alkoxycarbonyl group, as defined above, attached to an amino group, such as methoxycarbonylamino, ethoxycarbonylamino, and the like. The term "aryloxycarbonylamino"used herein, alone or in combination with other radicals, denotes an aryloxycarbonyl group, as defined above, attached to the an amino group, such as C6H5OCONH, C6H5OCONCH3, C6H5OCONC2H5, C6H4 (CH30) CONH, C6H4 (OCH3) OCONH, and the like. The term"aralkoxycarbonylamino"used herein, alone or in combination with other radicals, denotes an aralkoxycarbonyl group, as defined above, attached to an amino group C6H5CH2OCONH, C6H5CH2CH2CH20CONH, C6H5CH20CONHCH3, C6H5CH20CONC2H5, C6H4 (CH3) CH2OCONH, C6H4 (OCH3) CH20CONH, and the like.

The term"aminocarbonylamino","alkylaminocarbonylamino", "dialkylaminocarbonylamino"used herein, alone or in combination with other radicals, denotes a carbonylamino (-CONH2) group, attached to amino (NH2), alkylamino group or dialkylamino group respectively, where alkyl group is as defined above.

The tem"hydrazino"used herein, either alone or in combination with other radicals, denotes-NHNH-, suitably substituted with other radicals, such as alkyl hydrazino, where an alkyl group, as defined above is attached to a hydrazino group.

The term"alkoxyamino"used herein, alone or in combination with other radicals, denotes an alkoxy group, as defined above, attached to an amino group. The term "hydroxyamino"used herein, alone or in combination with other radicals, denotes- NHOH moiety, and may be substituted.

The term"sulfenyl"or"sulfenyl and its derivatives"used herein, alone or in combination with other radicals, denotes a bivalent group, -SO-or RSO, where R is substituted or unsubstituted alkyl, aryl, heteroaryl, heterocyclyl, and the like.

The term"sulfonyl"or"sulfones and its derivatives"used herein, either alone or in combination with other radicals, with other terms such as alkylsulfonyl, denotes divalent radical-SO2-, or Rus02-, where R is substituted or unsubstituted groups selected from alkyl, aryl, heteroaryl, heterocyclyl, and the like."Alkylsulfonyl"denotes alkyl radicals, as defined above, attached to a sulfonyl radical, such as methylsulfonyl, ethylsulfonyl, propylsulfonyl and the like. The term"arylsulfonyl"used herein, either alone or in combination with other radicals, denotes aryl radicals, as defined above, attached to a sulfonyl radical, such as phenylsulfonyl and the like.

Suitable groups and substituents on the groups may be selected from those described anywhere in the specification.

Particularly useful compounds of the present invention are: <BR> <BR> <BR> <BR> (S)-N- [3- (3-Fluoro-4- {4- [3- (4-hydroxyphenyl)-acryloyl]-piperazin-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] acetamide; <BR> <BR> <BR> <BR> (S) -N- [3- (3-Fluoro-4- {4- [3- (4-hydroxyphenyl)-acryloyl]-piperazin-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] thioacetamide; <BR> <BR> <BR> <BR> (S)-N- [3- (3-Fluoro-4- {4- [3- (4-hydroxyphenyl)-acryloyl]-piperazin-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl thiourea; <BR> <BR> <BR> <BR> (S)-N- [3- (3-Fluoro-4- {4- [3- (3-hydroxyphenyl)-acryloyl]-piperazin-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] acetamide; <BR> <BR> <BR> <BR> (S)-N- [3- (3-Fluoro-4- {4- [3- (3-hydroxyphenyl)-acryloyl]-piperazin-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] thioacetamide; <BR> <BR> <BR> <BR> (S)-N- [3- {4- (4- (3-Benzo [1, 3]-dioxol-5-yl-acryloyl)-piperazin-1-yl}-3-fluorophenyl]-2- oxo-oxazolidin-5-yl methyl] acetamide ; <BR> <BR> <BR> <BR> (S)-N- [3- {4- (4- (3-Benzo [1, 3]-dioxol-5-yl-acryloyl)-piperazin-1-yl}-3-fluorophenyl]-2- oxo-oxazolidin-5-yl methyl] thioacetamide; <BR> <BR> <BR> <BR> (S)-N- [3- {4- (4- (3-Benzo [1, 3]-dioxol-5-yl-acryloyl)-piperazin-1-yl}-3-fluorophenyl]-2- oxo-oxazolidin-5-yl methyl thiourea;

(S)-N-[3-(3-Fluoro-4-{4-[3-(thiophen-3-yl)-acryloxy]-piperaz inyl]-phenyl)-2-oxo- oxazolidin-5-yl methyl]acetamide; (S)-N-[3-(3-Fluoro-4-{4-[3-(thiophen-2-yl)-acryloxy]-piperaz inyl]-phenyl)-2-oxo- oxazolidin-5-yl methyl]acetamide; (S)-N-[3-(3-Fluoro-4-{4-[3-(thiophen-2-yl)-acryloxy]-piperaz inyl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] thioacetamide; (S)-N-[3-(3-Fluoro-4-{4-[3-(thiophen-3-yl)-acryloxy]-piperaz inyl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] thiourea; (S)-N-[3-(3-Fluoro-4-{4-[3-(thiophen-3-yl)-acryloxy]-piperaz inyl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] thiocarbamate; (S)-N-[3-(3-Fluoro-4-{4-[3-(1H-indol-3-yl)-acryloxy]-piperaz in-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl]acetamide; (S)-N-[3-(3-Fluoro-4-{4-[3-(1H-indol-3-yl)-acryloxy]-piperaz in-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] thioacetamide; (S)-N-[3-(3-Fluoro-4-{4-[3-(1H-indol-3-yl)-acryloxy]-piperaz in-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] thiourea; (S)-N-[3-(3-Fluoro-4-{4-[3-(furan-2-yl)-acryloxyl]-piperazin -1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl]acetamide; (S)-N-[3-(3-Fluoro-4-{4-[3-(furan-2-yl)-acryloxyl]-piperazin -1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] thioacetamide; (S)-N-[3-(3-Fluoro-4-{4-[3-(furan-2-yl)-acryloxyl]-piperazin -1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl ]thiourea; (S)-N-[3-(3-Fluoro-4-{4-[3-(pyridin-3-yl)-acryloxy]-piperazi n-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl]acetamide; (S)-N-[3-(3-Fluoro-4-{4-[3-(pyridin-3-yl)-acryloxy]-piperazi n-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] thioacetamide; (S)-N-[3-(3-Fluoro-4-{4-[3-(pyridin-4-yl)-acryloxy]-piperazi n-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl]acetamide; (S)-N-[3-(3-Fluoro-4-{4-[3-(pyridin-4-yl)-acryloxy]-piperazi n-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] thioacetamide; (S)-N-[3-(3-Fluoro-4-{4-[3-(pyridin-4-yl)-acryloxy]-piperazi n-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl ]thiourea; (S)-N-[3-(3-Fluoro-4-{4-[3-(phenyl-propanoyl]-piperazin-1-yl ]-phenyl)-2-oxo- oxazolidin-5-yl methyl]acetamide;

(S)-N- [3- (3-Fluoro-4- {4- [3-phenyl-propanoyl]-piperazin-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyls thioacetamide; (S)-N- [3- (3-Fluoro-4- {4- [3- (4-fluorophenyl)-acryloyl]-piperazin-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] acetamide ; (S)-N- [3- (3-Fluoro-4- {4- [3- (4-fluorophenyl)-acryloyl]-piperazin-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] thioacetamide ; (S)-N- [3- (3-Fluoro-4- {4- [3- (4-fluorophenyl)-acryloyl]-piperazin-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] thiourea; <BR> <BR> <BR> <BR> (S)-N- [3- (3-Fluoro-4- {4- [3- (4-fluorophenyl)-acryloyl]-piperazin-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyls thiocarbamate ; <BR> <BR> <BR> <BR> (S) -N- [3- (3-Fluoro-4- {4- [3-phenyl acryloyl]-piperazin-1-yl]-phenyl)-2-oxo-oxazolidin- 5-yl methyl] acetamide ; (S)-N- [3- (3-Fluoro-4- {4- [3-phenyl acryloyl] -piperazin-1-yl]-phenyl)-2-oxo-oxazolidin- 5-yl methyl] thioacetamide ; <BR> <BR> <BR> <BR> (S) -N- [3- (3-Fluoro-4- {4- [3-phenyl acryloyl]-piperazin-1-yl]-phenyl)-2-oxo-oxazolidin- 5-yl methyl] thiourea; (S)-N- [3- (3-Fluoro-4- {4- [3- (4-methoxyphenyl) acryloyl) -piperazin-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] acetamide ; <BR> <BR> <BR> <BR> (S)-N- [3- (3-Fluoro-4- {4- [3- (4-methoxyphenyl) acryloyl)-piperazin-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] thioacetamide ; (S)-N- [3- (3-Fluoro-4- {4- [3- (4-methoxyphenyl) acryloyl) -piperazin-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] thiourea; <BR> <BR> <BR> <BR> (S)-N- [3- (3-Fluoro-4- {4- [3- (4-acetoxyphenyl) acryloyl)-piperazin-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] acetamide; (S)-N- [3- (3-Fluoro-4- {4- [3- (4-acetoxyphenyl) acryloyl) -piperazin-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] thioacetamide; <BR> <BR> <BR> <BR> (S)-N- [3- (3-Fluoro-4- {4- [3- (4-acetoxyphenyl) acryloyl)-piperazin-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] thiourea; (S)-N- [3- (3-Fluoro-4- {4- [3-furan-3-yl-acryloyl)-piperazin-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] acetamide; (S)-N- [3- (3-Fluoro-4- {4- [3- (3, 4-difluorophenyl)-acryloyl)-piperazin-1-yl]-phenyl)-2- oxo-oxazolidin-5-yl methyl] acetamide; (S)-N- [3- (3-Fluoro-4- {4- [3- (3, 4-difluorophenyl)-acryloyl)-piperazin-1-yl]-phenyl)-2- oxo-oxazolidin-5-yl methyl] thioacetamide;

(S)-N- [3- (3-Fluoro-4- {4- [3- (3, 4-difluorophenyl)-acryloyl)-piperazin-1-yl]-phenyl)-2- oxo-oxazolidin-5-yl methyl] thioacetamide ; Methanesulfonic acid 4- [3- (4- {4- [5- (acetyl aminomethyl)-2-oxo-oxazolidin-3-yl]-2- fluorophenyl} piperazin-1-yl]-3-oxo-propenyl]-phenyl ester; (S)-N- [3- (3-Fluoro-4- {4- [3- (4-methylsulfanyl-phenyl)-acryloyl)-piperazin-1-yl]-phenyl)- 2-oxo-oxazolidin-5-yl methyl] acetamide; (S)-N- [3- (4- {4- [3- (3, 4-dihydroxyphenyl)-acryloyl)-piperazin-1-yl]-3-fluorophenyl) -2- oxo-oxazolidin-5-yl methyl] acetamide ; (S)-N- [3- (4- {4- [3-biphenyl-4-yl-acryloyl)-piperazin-1-yl]-3-fluorophenyl)-2 -oxo- oxazolidin-5-yl methyl] acetamide ; (S)-N- [3- (4- {4-but-2-enoyl-piperazin-1-yl]-3-fluorophenyl)-2-oxo-oxazoli din-5-yl methyl] acetamide ; (S)-N- [3- (4- {4-acryloyl-piperazin-1-yl]-3-fluorophenyl)-2-oxo-oxazolidin -5-yl methyl] acetamide; (S)-N- [3- (3-Fluoro-4- {4- [2-methylacryloyl-piperazin-1-yl]-phenyl)-2-oxo-oxazolidin-5 - yl methyl] acetamide; (S)-N- [3- (-4- {4- [3- (4-benzyloxy-phenyl)-acryloyl)-piperazin-1-yl]-3-fluoropheny l)-2- oxo-oxazolidin-5-yl methyl] thiourea; (S)-N- [3-(4- {4- [3-(4-nitrophenyl)-acryloyl)-piperazin-1-yl]-3-fluorophenyl) -2-oxo- oxazolidin-5-yl methyl] acetamide; Carbonic acid-1- {4- [3- (4- {4- [5- (acetylamino-methyl)-2-oxo-oxazolidin-3-yl]-2- fluorophenyl}-piperazin-1-yl)-3-oxo-propenyl]-phenoxy}-ethyl ether cyclohexyl ester; (S)-N- [3- (4- {4- [3- (4-aminophenyl)-acryloyl)-piperazin-1-yl]-3-fluorophenyl)-2- oxo- oxazolidin-5-yl methyl] acetamide ; <BR> <BR> <BR> <BR> (S)-N- [3- (4- {4- [3- (3, 4-diacetoxy-phenyl)-acryloyl)-piperazin-1-yl]-3-fluorophenyl )-2- oxo-oxazolidin-5-yl methyl] acetamide; (S)-N- [3- (4- {4- [3-benzo [1, 3] -dioxol-5-yl acryloyl)-piperazin-1-yl]-3-fluorophenyl)-2- oxo-oxazolidin-5-yl methyl] thiocarbamate; (S)-N- [3- (3-Fluoro-4- [4- (4-oxo-4-phenyl-but-2-enoyl)-piperazin-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] acetamide; (S) -N- [3- (3-Fluoro-4- [4- (4- (4-methoxyphenyl)-4-oxo-but-2-enoyl)-piperazin-1-yl]- phenyl)-2-oxo-oxazolidin-5-yl methyl] acetamide; (S) -N- [3- (3-Fluoro-4- [4- (4- (4-methoxyphenyl)-4-oxo-but-2-enoyl)-piperazin-1-yl]- phenyl) -2-oxo-oxazolidin-5-yl methyl] thioacetamide;

(S)-N- [3- {4- [4- (4- (4-acetylaminophenyl)-4-oxo-but-2-enoyl)-piperazin-1-yl]-3- fluorophenyl)-2-oxo-oxazolidin-5-yl methyl] acetamide; (S) -N- [3- (3-Fluoro-4- [4- (4- (4-acetylaminophenyl)-acryloyl)-piperazin-1-yl]-3- fluorophenyl)-2-oxo-oxazolidin-5-yl methyl] acetamide; <BR> <BR> <BR> <BR> (S) -N- [3- (3-Fluoro-4- [4- (3-cyclohexyl)-acryloyl-piperazin-1-yl]-3-fluorophenyl)-2-ox o- oxazolidin-5-yl methyl] acetamide; Acetic acid-2- (4- {4- [5-(acetylaminomethyl)-2-oxo-oxazolidin-3-yl]-2-fluorophenyl ] [- piperazinyl-1-carbonyl-7-amino-3-oxo-5-thia-1-aza-bicyclo- [4. 2. 0]-oct-2-en-3-yl-methyl ester; 2,2-Dimethyl-propanoic acid-4- (3- (4- {4- [5- (acetylaminomethyl)-2-oxo-oxazolidin-3-yl]- 2-fluorophenyl} piperazinyl-1-yl)-3-oxo-propenyl]-phenyl ester; Carbonic acid-1- {4- [3- (4- {4- [5- (acetylaminomethyl)-2-oxo-oxazolidin-3-yl]-2- fluorophenyl] [-piperazinyl-1-yl) -3-oxo-propenyl]-phenyl ester; <BR> <BR> <BR> <BR> (S)-N- [3- (3-Fluoro-4- [4- (3- (5-nitrofuran-2-yl)-acryloyl-piperazin-1-yl]-3-phenyl)-2-oxo - oxazolidin-5-yl methyl] acetamide; (S)-N- [3- (3-Fluoro-4- [4- (6-methoxy-l-oxo-1, 2,3, 4 tetrahydronaphthalen-2-yl methyl)- piperazin-1-yl]-phenyl)-2-oxo-oxazolidin-5-yl methyl] acetamide; (S)-N- [3- (3-Fluoro-4- [4- (1-oxo-1, 2,3, 4 tetrahydronaphthalen-2-yl methyl)-piperazin-1- yl]-3-phenyl)-2-oxo-oxazolidin-5-yl methyl] acetamide; (S)-N- [3- (3-Fluoro-4- [4- (5-methoxy-1-oxo-indan-2-yl-methyl)-piperazin-1-yl]-3- phenyl)-2-oxo-oxazolidin-5-yl methyl] acetamide ; (S)-N- [3- (3-Fluoro-4- [4- (2-oxo-cyclohexylmethyl)-piperazin-1-yl]-3-phenyl)-2-oxo- oxazolidin-5-yl methyl] acetamide; (S)-N- [3- (3-Fluoro-4- [4- (6-methoxy-1-oxo-1, 2,3, 4 tetrahydronaphthalen-2-yl methyl)- piperazin-1-yl]-3-phenyl)-2-oxo-oxazolidin-5-yl methyls thioacetamide; (S) -N- [3- (3-Fluoro-4- [4- (5-methoxy-1-oxo-indan-2-yl-methyl)-piperazin-1-yl]-3- phenyl) -2-oxo-oxazolidin-5-yl methyl] thioacetamide ; (S)-N- [3- (3-Fluoro-4- [4- (1-hydroxyimino-6-methoxy-1, 2,3, 4 tetrahydronaphthalen-1-yl methyl)-piperazin-1-yl]-phenyl)-2-oxo-oxazolidin-5-yl methyl] acetamide ; (S)-N- [3- (3-Fluoro-4- [4- (4-methyl-1-oxo-1, 2,3, 4 tetrahydronaphthalen-2-yl methyl)- piperazin-1-yl] -phenyl) -2-oxo-oxazolidin-5-yl methyl] thioacetamide ; <BR> <BR> <BR> <BR> Trans- (S)-N- (3- {3-Fluoro-4- [4- (3-1H-pyrrol-2-yl-acryloyl)-piperazin-1-yl]-phenyl}-2- oxo-oxazolidin-5-yl-methyl) acetamide.

Cis- (S)-N- (3- {3-Fluoro-4- [4- (3-lH-pyrrol-2-yl-acryloyl)-piperazm-l-yl]-phenyl}-2-oxo- oxazolidin-5-yl-methyl) acetamide.

(S)-5- [3- (4- {4- [5- (Acetylamino-methyl)-2-oxo-oxazolin-3-yl]-2-fluoro-phenyl}- piperazin-1-yl)-3-oxo-propenyl]-furan-2-carboxlic acid sodium salt (S)-5- [3- (4- {4- [5- (Acetylamino-methyl)-2-oxo-oxazolin-3-yl]-2-fluoro-phenyl}- piperazin-1-yl)-3-oxo-propenyl]-furan-2-carboxlic acid.

(S)-N-[3-(3-Fluoro-4-{4-[3-(5-hydroxymethyl-furan-2-yl)-a cryloxy]-piperazin-1-yl}- <BR> <BR> <BR> <BR> phenyl)-2-oxo-oxazolidin-5-yl methyl] acetamide.<BR> <BR> <BR> <BR> <BR> <BR> <BR> <P>(S)-N- [3- (3-Fluoro-4- {4- [3- (4-methanesulfonyl-phenyl)-acryloyl]-piperazin-1-yl}- phenyl)-2-oxo-oxazolidin-5-yl methyl] acetamide.

(S)-4-(4-{4-[5-(Aceylamino-methyl)-2-oxo-oxazolidin-3-yl] -2-fluoro-phenyl}-piperazin- 1-yl)-4-oxo-but-2-enoic acid.

(S)-N- [3- (3-Fluoro-4- {4- [3- (5-formyl-furan-2-yl)-acryloyl]-piperazin-1-yl}-phenyl)-2- oxo-oxazolidin-5-yl methyl] acetamide.

(S) -Acetic acid-5- [3- (4- {4- [5- (Acetylamino-methyl)-2-oxo-oxazolin-3-yl]-2-fluoro- phenyl}-piperazin-1-yl)-3-oxo-propenyl]-furan-2-yl methyl ester.

(S)-4- (4-{4-[5-(Aceylamino-methyl)-2-oxo-oxazolidin-3-yl]-2-fluoro -phenyl}-piperazin- 1-yl)-4-oxo-but-2-enoic acid sodium salt. <BR> <BR> <BR> <BR> <P>(S)-N- [3- (3-Fluoro-4- {4- [3- (5-methyl-furan-2-yl)-acryloyl]-piperazin-1-yl}-phenyl)-2- oxo-oxazolidin-5-yl methyl] acetamide.

(S)-N- [3- (3-Fluoro-4- {4-propynoyl-piperazin-1-yl]-phenyl)-2-oxo-oxazolidin-5-yl methyl] acetamide; (S)-N- [3- (3-Fluoro-4- {4- (4-hydroxy-but-2-enoyl)-piperazin-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] acetamide ; (S)-N- [3- (3-Fluoro-4- {4- (4-bromo-but-2-enoyl)-piperazin-1-yl]-phenyl)-2-oxo- oxazolidin-5-yl methyl] acetamide; 2- [4-(4- {5-(acetylamino-methyl)-2-oxo-oxazolidin-3-yl}-2-fluoropheny l)-piperazin-1- carbonyl]-3-phenyl-acrylic acid methyl ester; 2- (4-{4-[5-(Aceylamino-methyl)-2-oxo-oxazolidin-3-yl}-2-fluoro phenyl)-piperazin-1- carbonyl] -3-phenyl-acrylic acid; 2- [4-(4- {5-(acetylamino-methyl)-2-oxo-oxazolidin-3-yl}-2-fluoropheny l)-piperazin-1- carbonyl] -3-furane acrylic acid methyl ester; 2- [4- (4-15- (acetylamino-methyl)-2-oxo-oxazolidin-3-yl}-2-fluorophenyl)- piperazin-l- carbonyl]-3-furane-acrylic acid;

The compounds of general formula (I) may be prepared by one or more routes or combinations of reactions given below and outlined in detail. The method comprises: i) Route 1: by reacting a compound of formula (la) with a compound of formula (lb) where R represents OH, halide or an acyloxy group, to yield compound of formula (I) where Y represents G2 and all symbols are as defined earlier. ii) Route 2: by reacting a compound of formula (1c) with a compound of formula (lb) to yield compounds of formula (1) ; where Y represents G1 and all symbols are as defined earlier. iii) Route 3: A process which comprises: a) reaction of a compound of formula (la) with a compound of formula (ld) to yield (1a) (1d) (1e) (le), where all symbols are as defined earlier;

b) Converting a compound of formulas (1e) to (1f) where L represents a leaving group such as-OMs, -OTs, halides etc. and all other symbols are as defined earlier; c) Converting a compound (1f) to (lg), where all symbols are as defined earlier; d) Converting a compound (1g) to (Ih), where all symbols are as defined earlier; e) Converting a compound (lh) to (li), where all symbols are as defined earlier ; f) Converting a compound (li) to (1j), where all symbols are as defined earlier; Alternatively,

g) Converting a compound (li) to (lk) where all symbols are as defined earlier; Alternatively h) Converting a compound (li) to (11), where all symbols are as defined earlier; Compounds of formula (Ie), (Ig), (Ih), (Ii), (Ij), (Ik), (11) represent compounds of formula (I), where all symbols are as defined earlier and W represents OH, N3, NH2, NCS, NHCSR7, NHCSSR7, NHCSOR7 respectively and Y represents G2 with X=O ; iv) Route 4: Reacting a compound of formula (lm) with a compound of formula (lb) to give compound of formula (1n), where all symbols are as defined earlier; The compound (In) is a compound of formula (I), where Y represents G3. The reactions described in the processes outlined above may be performed by using the methods described herein: Route 1:

Compounds of general formula I may be obtained from compound of general formula (Ia) by coupling with compound of general formula (Ib), employing different coupling agents depending upon the nature of (Ia) such as acid chlorides or mixed anhydrides corresponding to (Ia). Bases such as Na2C03, K2C03 and the like; organic bases like triethylamine, pyridine, diisopropylethylamine and the like; solvents such as acetone, THF may be used. Temperature in the range of-20 °C to reflux temperature of the solvent may be used. If (Ia) is an acid, suitable coupling agents like DCC, HOBT and the like may be used. Solvents such as dichloromethane, chloroform may be used.

Route 2: Compounds of general formula I may be obtained by reacting compounds of general formula (Ic) with compounds of general formula (Ib), in presence of formaldehyde or paraformaldehyde and HCl in methanol or ethereal HC1 or 1,3 dioxalane and conc. HCI.

Solvents such as THF, Diethyl ether may be used. Temperature in the range of 0 °C to reflux temperature of the solvent may be used.

Route 3: a) Compounds of general formula (Ie) may be obtained from compounds of general formula (Ia) by coupling with compounds of general formula (Id), employing different sets of coupling agents depending upon the nature of (Ia) such as acid chlorides corresponding to (Ia), and bases such as Na2CO3, K2C03 and the like; organic bases like triethylamine, pyridine, diisopropylethylamine and the like; Solvent such as acetone, THF may be used. Temperature in the range of-20 °C to reflux temperature of the solvent may be used. If (Ia) is an acid, suitable coupling agents like DCC, HOBT and the like may be used. Solvents such as dichloromethane, chloroform may be used.

b) Compounds of general formula (If) may be obtained by treating the compounds of general formula (Ie), with appropriate sulfonyl chloride such as p-Ts-chloride, MsCI, benzene sulfonyl chloride and the like to get sulfonyl esters in presence of bases like triethylamine, pyridine, K2CO3 and the like or mixture thereof. Solvents such as DMF, DMSO, dichloromethane, dichloroethane, pyridine and the like and the mixtures thereof may be used. The temperature may range from 0 °C to reflux temperature of the solvent, preferably between 5 °C to 40 °C.

Alternatively, the compounds of general formula (If), where L is halide, may be obtained by treating the compounds of general formula (Ie) with SOC12, POCl3, PCIs, PBr3 and the like, HBr/red P, in the presence of solvents such as DMF, DMSO, THF, benzene, CH2C12, dichloroethane and the like. The temperatures may range from 0 °C to 50 °C. The mole ratio of halogenating agent to compounds (Ie) can range from 1: 1 to 1: 1.5. c) Compounds of general formula (Ig) may be obtained by treating the compounds of general formula (If) with metal azides in solvents such as DMSO, pyridine, DMF and the like may be used. Temperature in the range of 10 °C to 120 °C may be used, preferably between 30 °C to 60 °C d). Compounds of general formula (Ih) can be obtained by (Ig) by use of triphenylphosphine and aquoues NH3 or H20 in solvents such as methanol, ethanol at temperatures between-10 °C to 30 °C. The molar ratio of compounds (Ig) and reducing agent can range from 1: 10 to 1: 25.

(tg) (ih) e) Compounds of general formula (li) can be obtained from compounds of general formula (Ih) by treating with carbon disulfide solution in presence of bases such as TEA & pyridine employing catalytic amount of esters of halogenated formic acid at temperatures between 0 °C and 50 °C depending upon the choice of bases.

(1 h) (i i) f) Compounds of general formula (Ij), where R7 is NH2, may be obtained from compounds of general formula (li) by treating it with ammonia in solvents such as methanol, ethanol and the like at temperatures ranging between-10 °C to 50 °C.

(1i) (1j) g) Alternatively, compound of general formula (Ik) may be obtained from compound of general formula (li) by treating it with solution of alkyl halides in solvents like ether or THF, at low temperature, preferably at 0-5 °C.

h) Alternatively, compound of general formula (Il) may be obtained from compound of general formula (li) by treating with metal hydrides such as sodium hydrides at low temperature in anhydrous alcohols as a solvent as well as a reactant.

Route 4: Compounds of general formula (Ib) when treated with compound of general formula (Im) in presence of metal carbonates such as K2CO3, Na2C03, Cs2CO3 in solvents such as acetone, THF, at temperature ranging from 0-40 °C preferably at ca. 5 °C, gives compound of general formula (ln).

Route 5: Compound of general formula (Ip) may be obtained from compounds of general formula (Io) by treating it with Lawesson's reagent in solvents such as THF, 1,4-dioxane, dichloromethane at temperature ranging from 30 °C to reflux temperature of the solvent being used..

Pharmaceutically acceptable salts means salts formed by the addition of acids useful for administering the compounds of the present invention and includes hydrochloride, hydrobromide, sulfate, bisulfate, phosphate, acetate, propionate, lactate, mesylate, maleate, succinate, tartarate, citrate, 2-hydroxyalkylsulfonate, fumarate, oxalate, ascorbate and the like when a basic group is present in compound of formula (I).

These salts may be in hydrated form-some of the compounds of the invention may form metal salts such as sodium, potassium, calcium and magnesium salts and these are embraced by the term"pharmaceutically acceptable salts".

It will be appreciated that in any of the above mentioned reactions any reactive group in the substrate molecule may be protected, according to conventional chemical practice.

Suitable protecting groups in any of the above mentioned reactions are those used conventionally in the art. The methods of formation and removal of such protecting groups are those conventional methods appropriate to the molecule being protected. T.

W. Greene and P. G. M. Wuts"Protective groups in Organic Synthesis", John Wiley & Sons, Inc, 1999, 3d Ed. , 201-245 along with references therein.

It will be appreciated that the above-mentioned preparation of the compounds of Formula (I), or a pharmaceutically acceptable salts thereof, and/or pharmaceutically acceptable solvates thereof employs (ld) or (lb) as a pure enantiomer to afford the compound of formula (I) as a single stereoisomer. Favorably, in a compound of formula (I) the preferred configuration at C-5 of the oxazolidinone ring of compounds claimed in the invention is (S) -under the Cahn-Ingold-Prelog nomenclature system. Since this (S)- enantiomer which is pharmacologically active. The racemic mixture is useful in the same way and for the same purpose as the pure (S) -enantiomers the difference lies in the fact that double as much racemic material will be required to produce the same antibacterial effect.

Because carbon-carbon double bond also exists in the compounds, the invention contemplates various geometric isomers and mixtures thereof resulting from the arrangement of substituents around these carbon-carbon double bonds. These substituents are designated as being in the E or

Z configuration wherein the term"E"refers to higher order substituents on opposite sides of the carbon-carbon double bond, and the term"Z"refers to higher order substituents on the same side of the carbon-carbon double bond. A thorough discussion of E and Z isomerism is provided in"Advanced Organic Chemistry. Reaction, Mechanisms, and Structure", 4th ed. , John Wiley & Sons, New York, 1992, pp. 109-112.

Preferably the compounds of Formula (I), or a pharmaceutically acceptable salt thereof, and/or pharmaceutically acceptable solvate thereof is in optically pure form.

The absolute stereochemistry of the compounds may be determined using conventional methods, such as X-ray crystallography.

Another aspect of the present invention comprises a pharmaceutical composition, containing at least one of the compounds of the general formula (I), their derivatives, their analogs, their tautomeric forms, their polymorphs, their prodrugs, their stereoisomers, their pharmaceutically acceptable salts, their pharmaceutically acceptable solvates thereof as an active ingredient, together with pharmaceutically employed carriers diluents and the like.

Pharmaceutical compositions containing a compound of the present invention may be prepared by conventional techniques, e. g. as described in Remington: the Science and Practice of Pharmacy, with Ed. , 1995. The compositions may be in the conventional forms, such as capsules, tablets, powders, solutions, suspensions, syrups, aerosols or topical applications. They may contain suitable solid or liquid carriers or in suitable sterile media to form injectable solutions or suspensions. The compositions may contain 0.5 to 20 %, preferably 0.5 to 10 % by weight of the active compound, the remaining being pharmaceutically acceptable carriers, excipients, diluents, solvents and the like.

The compounds of Formula I are useful in the treatment of microbial infections in humans and other warm blooded animals, by either oral, topical or parenteral administration.

Besides being useful for human treatment, these compounds are also useful for veterinary treatment of companion animals, exotic animals and farm animals including mammals, rodents, and the like. More preferred animals include horses, dogs and cats.

For the treatment of any of the above-mentioned diseases the compounds of formula (I) may be administered, for example, orally, topically, parenterally, in dosage unit formulations containing conventional non-toxic pharmaceutically acceptable carriers, adjuvants and vehicles.

The pharmaceutical composition is provided by employing conventional techniques.

Preferably the composition is in unit dosage form containing an effective amount of the active component, that is, the compounds of formula I according to this invention.

The quantity of active component, that is, the compounds 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 method, the potency of the particular compound and 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 bacterial infections in humans and animals that have been diagnosed with having bacterial infections, the compounds or pharmaceutical compositions thereof will be administered orally, parenterally and/or topically at a dosage to obtain and maintain a concentration, that is, an amount, or blood-level of active component in the animal undergoing treatment which will be antibacterially active. Generally, such antibacterially effective amount of dosage of active component will be in the range of about 0.1 to about 100 mg/kg, more preferably about 3.0 to about 50mg/kg of body weight/day. However, it should be appreciated that the dosages may vary depending upon the requirements of the patient, the severity of the bacterial infection, and the particular compound being used. Also, it must be understood that the initial dosage administered may be increased beyond the upper level in order to rapidly achieve the desired blood level or the initial dosage may be smaller than the optimum and the 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 administered, e. g. two to four times per day.

The compounds of the present invention may be administered alone or in combination with pharmaceutically acceptable carriers or diluents by any of the routes as previously indicated, in single or multiple doses. More specifically, the novel compounds described in the invention can be administered in a wide variety of different dosage forms, i. e. , they may be combined with various pharmaceutically acceptable inert carriers in the form of tablets, capsules, lozenges, trochees, hard candies, powders, sprays, creams, salves, suppositories, jellies, gels, pastes, lotions, ointments, aqueous suspensions, injectable solutions, elixirs, syrups, and the like. The carriers may include solid diluents or fillers, sterile aqueous media and various nontoxic organic solvents etc. Moreover, for oral consumption, the pharmaceutical compositions can be suitably sweetened and/or flavored. In general, the therapeutically-effective compounds as described in the invention are present in the compositions at concentration levels ranging from 5% to 60% by weight, preferably 10% to 50% by weight.

For oral administration, the tablets may be combined with various excipients such as microcrystalline cellulose, sodium citrate, calcium carbonate, dipotassium phosphate and glycine along with various disintegrants such as starch more preferably corn, potato or tapioca starch, alginic acid, sodium carbonate and certain complex sillicates; together with binders like polyvinylpyrrolidone, sucrose, gelatin and acacia, humectants such as for example, glycerol; solution retarding agents, such as, for example paraffin; absorption accelerators such as, for example, quartenary ammonium compounds; wetting agents like cetyl alcohol and glycerol monostearate ; absorbents like kaolin and bentonite clay. Additionally, magnesium stearate, sodium lauryl sulfate, talc, calcium stearate, solid polyethylene glycols and mixtures thereof are often added as lubricating agents for tabletting purposes. In the case of capsules, tablets and pills, the dosage form may also comprise buffering agents.

Similar type of solid compositions may also be employed as fillers and excipients in soft and hard gelatine capsules; preferred materials includes lactose, milk sugar or high molecular weight polyethylene glycols.

The active compounds can also be in micro-encapsulated form using one or more of the excipients noted above. The solid dosage forms of tablets, dragees, capsules, pills, and the granules can be prepared with coatings and shells such as enteric coatings, release controlling coatings and other coatings which are well known in the field of pharmaceutical formulation art. In such solid dosage forms the active compound may be admixed with atleast one inert diluent such as sucrose, lactose and starch. They may also contain, additional substances for e. g. tableting lubricants and other substances like magnesium stearate and microcrystalline cellulose. In the case of capsules, tablets, and pills, the formulation may also contain buffering agents. They may also be so formulated that they release the active ingredient (s) only or preferentially in a certain part of the intestinal tract, optionally in a delayed manner. The same may be achieved using embedded agents like, for example, polymeric substances and waxes.

Liquid dosage forms for oral administration include pharmaceutically acceptable emulsions, microemulsions, solutions, suspensions, syrups, and elixirs. For such oral consumption it is desirable to combine the active ingredient with various sweetening or flavoring agents, coloring matter or dyes, if so desired. The diluents may be selected from water, ethanol, propylene glycol, isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, 1,3 butylene glycol, dimethyl formamide, oils for e. g. cottonseed, groundnut, corn, germ, olive, castor, sesame oils and the like, glycerol, tetrahydrofurfuryl alcohol, polyethylene glycols and esters of fatty acids like sorbitan and various combination thereof. For mammals other than humans, the composition of the active substance are suitably modified.

For parenteral administration, the solutions of the compound is prepared in either sesame or peanut oil or in aqueous propylene glycol. The aqueous solutions should be suitably buffered (preferably pH>8) if necessary, and the diluent should be first rendered isotonic.

The aqueous solutions are suitable for intravenous injection purposes while the oily solutions are suitable for intra-articular, intra-muscular and subcutaneous injection purposes. The aforesaid compositions can be readily prepared under sterile conditions following well known standard pharmaceutical techniques by persons skilled in the art.

For buccal administration the composition may take the form of tablets or lozenges formulated in conventional manner.

For transdermal and topical administration, the dosage forms will include ointments, pastes, creams, lotions, gels, powders, solutions, sprays and inhalants. Transdermal patches may be prepared following standard drug delivery techniques and applied to the skin of a mammal, preferably a human or a dog, to be treated. Ophthalmic solutions, ear drops, eye ointments, powders can also be used as a medium of providing therapeutic dosages to the patients as will be necessary.

The ointments, pastes, creams and gels may, in addition to the active ingredient, contain excipients like animal and vegetable fats, oils, waxes, paraffins, starch, tragacanth, cellulose derivatives, polyethylene glycols, silicones, bentonites, silicic acid, talc, zinc oxide or their mixtures.

Powders and sprays may contain, in addition to the active substance, excipients like lactose, talc, silicic acid, aluminium hydroxide, calcium silicates and polyamide powder, or their mixtures. Sprays will additionally contain propellants like chlorofluorohydrocarbons.

The pharmaceutically acceptable compounds of the present invention are useful antibacterial agents having a good spectrum of activity in vitro and against standard Gram-positive organisms, which are used to screen for activity against pathogenic bacteria. Notably, the pharmaceutically acceptable compounds of the present invention show activity against enterococci, pneumococci, and methicillin resistant strains of S. aureus and coagulase negative staphylococci, together with morganella strains. The antibacterial spectrum and potency of a particular compound may be determined in a standard test system. The activity is described in terms of the minimum inhibitory concentration (MIC) determined by microbroth dilution technique as per NCCLS standards.

Determination of Antibacterial activity: The minimum inhibitory concentrations (MIC's) of the compounds for the microorganisms listed in Table A were determined by preparing working solution for

each compound of concentration of 128ßg/ml after dissolving it in DMSO. Two-fold serial dilution of the above solution was prepared in duplicates, using Mueller Hinton Broth, in 96 well Tissue culture plate with cover flat bottom wells to give a final volume of 150ug/ml and concentration of compound ranging from 64µg/ml-0.12µg/ml. 30µg/ml of Standard suspension of each organism which was prepared with turbidity equivalent to the 1: 10 diluted 0.5 McFarland standard with density 10 CFU/ml, was added to each well to get approximately a density of 105 CFU/ml. These 96-well Tissue culture plate containing the test samples and positive and negative controls, were incubated at 37°C for 16-18hrs. The wells were visually inspected for growth and were also read at 630nm by Automated Microplate Reader [ (EL800) Trinity biotech.] and the MIC's were recorded as the lowest concentration of drug which inhibits the growth of bacteria. The compounds inhibited the growth of these bacteria with MIC's in a range of about 0. 25, ug/ml to about 641lg/ml.

Thus the compounds are useful for treating bacterial infections such as, but not limited to, those shown below in Table A.

Table A Microorganism Methicillin resistant Staphylococcus aureus (ZYABL 006) Staphylococcus epidermidis ATCC 12228 Enterococcus faecalis ATCC 29212 Staphylococcus aureus ATCC 33591 Staphylococcus aureus MTCC 737/ATCC 6538P The invention is explained in detail by the examples given below, which are provided by way of illustration only and therefore should not be construed to limit the scope of the invention.

1 HNMR spectral data given in the tables (vide infra) are are recorded using a 300 MHz spectrometer (Bruker AVANCE-300) and reported in d scale. Until and otherwise mentioned the solvent usedfor NMR is CDCI3 using Tetramethyl silane as the internal standard.

Preparation 1

(S)-N- [3- (3-Fluoro-4- {4- [3- (thiophen-2-yl)-acryloyl] piperazinyl]-phenyl)-2-oxo- oxazolidin-5-yl-methyl] acetamide. (compound no. 01) To a solution of (S)-N- [ [3- [3-fluoro-4- (N-piperazinyl) phenyl]-2-oxo-5- oxazolidinyl] methyl] acetamide (J Med. Chem. 1996,39, 673-679) (0. 1 g) in chloroform (20 ml) was added. HOBt. H20 (0.1 g), 1- (3-dimethyl aminopropyl)-3- ethylcarbodiimide hydrochloride (0.1 g) followed by 3-(2-thienyl) acrylic acid (0. 045 g).

The reaction mixture was stirred at ca 27 °C to which triethylamine (lml) was added.

After stirring for 2 hrs. at ca 27 °C (TLC) the reaction mixture was diluted with CHC13 (30 ml. ) and washed with DM water (50 ml). Organic layer was separated, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude product was crystallized in EtOAc to afford the title compound as a white solid (75 mg, 53%) m. p. 223-225 °C.

The following compounds were prepared following the above procedure.

Table 1: 1. Z R4 R3 Mol. Wt. Yield cs -H H 472 53% 7. 8 (1H, d, J = 15. 06 Hz), 7. 4 (2H, dd, J = 2. 51 Hz), 7. 3 (2H, d, J = 5. 04 Hz), 7. 2 (1H, d, J = 3. 4 Hz), 7. 0 (2H, dd, J = 3. 48 Hz),), 6. 9 ( t, J = 9 Hz), 6. 7 (2H, d, J =15 Hz), 4. 8 (1H, m), 3. 9 (1H, t, J = 9. 0 Hz), 3. 7 (7H, m), 3. 2 (2H, m), 3. 0 (4H, t), 2. 2 (3H, s). 2. Mol d H H 467 80% N 8. 7 (1H, d, J=1. 71 Hz), 8. 5 (1H, d, J=3. 86 Hz) 8. 1 (1H, d, J=8. 04 Hz), 7. 6 (2H, d, J=15. 57 Hz), 7. 5 (2H, m), 7. 2 (1H, d, J=15. 57 Hz), 7. 1 (1H, dd, J=1. 86 Hz), 7. 0 (1H, t, J=9. 12 Hz), 4. 8 (1H, t, J=9 Hz), 4. 7 (1H, m), 4. 0 (1H, t, J=9. 0 Hz), 3. 9 (4H, t), 3. 7 (4H, m), 3. 5 (2H, d, J=4. 95 Hz), 3. 1 (4H, t), 1. 95 (3H, s) ; (solvent used is CD30D+CDC13) 3. H H Mol. Wt Yield 390 120% 7. 4 (1H, dd, J=6. 12 Hz), 7. 0 (2H, d, J=8. 7 Hz), 6. 9 (1H, m), 6. 0 (1H, t), 4. 7 (lH, m), 4. 0 (1H, t), 3. 7 (5H, m), 3. 0 (8H, complex) 2. 02 (3H, s) 4. H H Mol. Wt Yield 496 47% Me 7. 6 (1H, dd, J=15. 33 Hz), 7. 4 (3H, m), 7. 0 (lH, dd, J=1. 71 Hz), 6. 9 (lH, d, J=15. 33 Hz), 6. 18 (lH, t, J=9. 6 Hz), 6. 7 (1H, d, J=15. 33 Hz), 6. 1 (lH, t), 4. 8 (lH, m), 4. 0 (1H, t), 3. 7 (1OH, complex), 3. 0 (1H, t), 3. 0 4H, t, J=4. 53 Hz), 2. 0 (3H, s) 5. w H H Mol. Wt Yield 4 482 52% Ho 7. 6 (1H, d, J=15. 3 Hz), 7. 3 (4H, m), 6. 9 (1H, t, J=9. 3 Hz), 6. 8 (2H, d, J=8. 4 Hz), 6. 7 (2H, d, J=15. 3 Hz), 4. 7 (1H, m), 3. 0 (4H, t), 2. 0 (3H, S), 4. 1 (2H, m), 3. 8 (4H, m), 3. 6 (4H complex) (solvent used is CD30D+CDC13) 6. H H Mol. Wt Yield 0 456 20% 7. 5 (3H, m), 7. 0 (1H, dd), 6. 9 (1H, t), 6. 8 (1H, d, J=15. 0 Hz), 6. 5 (1H, d, J=3. 3 Hz), 6. 4 (1H, dd), 5. 9 (1H, t), 4. 8 (1H, m), 4. 0 (2H, t, J=8. 97 Hz), 3. 8 (4H, d), 3. 7 (3H, complex), 3. 0 (4H, t), 2. 0 (3H, s). 7./\/\ H H Mol. Wt Yield 542 39% 7. 6 (1H, dd, J=12. 99 Hz), 7. 6 (6H, m), 7. 4 (4H, m), 7. 0 (1H, dd), 6. 9 (1H, d, J=12. 39 Hz), 5. 9 (1H, t), 4. 7 (1H, m), 4. 0 (1H, t, J=9 Hz), 3. 8 (4H, d), 3. 6 (3H, m), 3. 1 (4H, t), 2. 0 (3H, s). 8. Me H H Mol. Wt Yield 404 72% 7. 48 (1H, dd, J=11. 61 Hz, J=2. 5 Hz), 7. 0 (2H, dd, J=8. 76), 6. 9 (2H, m), 6. 2 (1H, dd, J=13. 32 Hz), 1. 65 Hz), 5. 9 (1H, t), 5. 3 (1H, m), 4. 0 (1H, t, J=8. 9 Hz), 3. 7 (6H, m), 3. 0 (4H, t, J=5. Hz), 2. 0 (3H, s), 1. 8 (3H, q, J=1. 56 Hz) 9. H H Me Mol. Wt Yield 404 71% 7. 4 (1H, dd, J=2. 55 Hz), 7. 0 (1H, dd, J=2Hz), 6. 51 Hz), 8. 9 (1H, t, J=9. 0 Hz), 5. 9 (1H, t), 5. 2 (1H, t, J=9. 0 Hz). 3. 7 (6H, m), 3. 0 (4H, s), 2. 0 (3H, s), 1. 9 (3H, s). 10. H H Mol. Wt Yield 560 58% Meo, So' 7. 6 (1H, d, J = 15. 4 Hz). 7. 5 (1H, dd, J=11. 85, Hz, 2. 31 Hz), 7. 4 (1H, d, J=8. 55 Hz), 2. 31 Hz), 6. 9 (2H, m), 6. 1 (1H, t), 4. 8 (1H, m), 4. 0 (1H, t, J=9 Hz), 3. 7 (6H, m), 3. 0 (3H, S), 2. 0 (3H, s). 11. H | H Mol. Wt Yield Fq 502 64% F 7. 6 (1H, d, J=15. 39 Hz), 7. 5 (1H, d, J=2. 52 Hz, 11. 61 Hz), 7. 4 (1H, d, J=2. 52 Hz, 11. 61 Hz), 7. 3 (4H, m), 7. 0 (2H, q, J=1. 77 Hz), 6. 9 (1H, t, J=9. 12 Hz), 6. 8 (1H, d, J=15. 42 Hz), 4. 7 (1H, m), 4. 0 (1H, t, J=9 Hz), 3. 9 (4H, t), 3. 6 (3H, m), 3. 3 (4H, t), 2. 0 (3H, s) 12. \o i H Mol. Wt Yield ou 510 77% 0 7. 8 (1H, t), 7. 6 (1H, d, J=15. 27 Hz), 7. 0 (3H, Hz), 6. 7 (1H, t), 6. 0 (2H, S), 4. 7 (1H, m), 4. 0 (1H, t, J=9. 0 Hz), 3. 8 (4H, m), 3. 5 (2H, t), 3. 0 (4H, m), 1. 9 3H, s solvent used is CD30D+CDC13-d6) 13. H H Mol. Wt Yield MeS I 512 88% 7. 6 (1H, d, J=15. 39 Hz), 7. 4 (3H, m), 7. 2 (2H, m), 7. 0 (1H, dd, J=1. 92 Hz, 8. 73 Hz), 6. 9 (1H, d, J=9. 0 Hz), 6. 8 (1H, d, J=15. 39 Hz), 6. 0 (1H, t), 3. 8 (1H, m), 4. 0 (1H, t, J=9 Hz), 3. 5 (6H, complex), 3. 0 (4H, t, J=4. 83 Hz), 2. 5 (3H, S), 2. 0 (3H, s) 14. H H Mol. Wt Yield 505 73% zon H 7. 9 (1H, d, J=15. 3 Hz), 7. 5 (2H, d), 7. 45 (2H, m), 7. 40 (1H, d, J=6. 93 Hz), 7. 0 (1H, dd, J=2. 04 Hz), 6. 9 (2H, d, J=9 Hz), 3. 7 (4H, t), 3. 6 (3H, m), 3. 1 (4H, t), 2. 02 (3H, s). 15. i I H H Mol. Wt Yield LJJ 482 70% OH 7. 6 (1H, d, J=15. 39 Hz), 7. 5 (1H, dd, J=2. 55 Hz, 11. 69 Hz), 7. 1 (1H, t, J=8. 0 Hz), 6. 8 (4H, m), 4. 7 (1H, m), 4. 0 (1H, t, J=9Hz), 3. 6 (6H complex), 3. 0 (4H, J=4. 8 Hz), 2. 0 (3H, s) ( (solvent used is CD30D+CDC13-d6) 16. ire H H Mol. Wt Yield 467 47% I 8. 6 (2H, d, J=5. 9 Hz), 8. 2 (1H, t, J=5. 8 Hz), 7. 6 (2H, d, J=6. 0 Hz), 7. 5 (3H, m), 7. 1 (1H, dd, J=6. 6 Hz, 2. 2 Hz), 7. 0 (t, 1H, J=9. 0 Hz), 4. 6 (1H, m), 4. 0 (2H, t), 3. 6 (5H, complex), 2. 9 (4H, t), 1. 8 (3H, S). (solvent used is DMSO-d6) 17. H H Mol. Wt Yield (sß 472 82% s 7. 7 (1H, d, J=15. 3 Hz), 7. 5 (4H, m), 7. 2 (1H, d), 6. 9 (1H, t, J=9. 0 Hz), 6. 7 (d, J=15. 27 Hz), 4. 7 (1H, m), 3. 0 (1H, t, J=9. 0 Hz), 3. 4 (7H, m), 3. 0 (4H, t, J=4. 82 Hz), 2. 0 (3H, s) (solvent used is CD30D+CDC13) 18. _ H H Mol. Wt Yield Hot 498 25% OH 7. 7 (1H, t), 7. 5 (1H, d, J=15. 3 Hz), 7. 4 (1H, dd, J=2. 5 Hz), 7. 0 (1H, dd, J=2 Hz), 6. 9 (3H, m), 6. 8 (1H, d, J=8. 16 Hz), 6. 7 (1H, d, J=15. 3 Hz), 4. 7 (1H, m), 4. 0 (1H, t, J=9Hz), 3. 6 (5H, complex), 3. 0 (4H, s), 2. 0 (3H, s) (solvent used is CD30D+CDC13) 19. 0 H H Mol. Wt Yield 566 85% (H3chc 7. 5 (1H, d, J=15Hz), 7. 5 (2H, d, J=8. 4Hz), 7. 49 (1H, dd, J=11. 64 Hz &2. 52 Hz), 7. 1 (4H, dd, J=8. 4Hz), 6. 9 (I H, t, J=9Hz), 6. 8 (1H, d, J=14. 9Hz), 6. 1 (1H, t), 4. 7 (1H, m), 4 (1H, t, J=9Hz), 3. 7 (7H, m), 3. 1 4H, t, J=1. 77Hz), 2 (3H, s) 1. 4 (9H, s). 20. ao 9H H Mol. Wt Yield 653 66% 7. 7 (1H, d, J=15. 4Hz) ; 7. 5 (2H, d, J=8. 65 Hz) ; 7. 4 (1H, dd, J=11. 73 & 2. 5 Hz) ; 7. 0 (1H, dd, J=2Hz) ; 6. 8 (2H, d, J=15. 14Hz) ; 5. 9 (1H, t) ; 4. 7 (2H, m) ; 4. 0 (1H, t, J=9) ; 3. 7 (7H, m) ; 3 (4H, t) ; 1. 98 su, m ; 1. 7 2H, t ; 1. 3 (4H, m). 21. H H Mol. Wt Yield 598 70% 7. 6 (1H, d, J=8. 58 Hz) ; 7. 5 (2H, d, J=14. 9Hz) ; 7. 4 (1H, dd, J=11. 64&2. 5Hz) ; 7. 2 (2H, d, J=15Hz) ; 7. 1 (1H, dd J=6. 9 & 1. 8Hz) ; 6. 9 (2H, m) ; 5. 9 (1H, t) ; 4. 7 (1H, m) ; 4. 35 (3H, q) ; 4 (1H, t, J=9Hz) ; 3. 7 (3H, m) ; 3. 1 (4H, t, J=4. 9Hz) ; 2. 01 (3H, s) ; 1. 4 (3H, t, J=7Hz). 22. H H Mol. Wt Yield ou 456 41% u 8. 24 (1H, d, J=5. 7 Hz) 8. 03 (1H, S), 7. 7 (1H, d), 7. 51 (lH, d, J=1. 8 Hz), 7. 13 (lH, d, J=12. 9 Hz), 7. 43 (lH, d, J=15. 9 Hz), 7. 04 (t, 141, 4. 6 (lH, m), 4. 07 (1H, t), 3. 69 (4H, t), 2. 97 (4H, t), 3. 8 (2H, t), 3. 38 (2H, t), 1. 81 (3H, s) (solvent used is DMSO-d6) 23. Fn/i H Mol. Wt Yield 484 73% F 7. 6 (1H, d, J=15. 4 Hz) ; 7. 5 (2H, m) ; 7. 4 (lH, d, J=2. 9Hz) ; 7. 0 (4H, m) ; 6. 9 (lH, t, J=9. lHz) ; 6. 8 (1H, d, J=15 Hz) ; 4. 7 (1H, m) ; 4 (lH, t, J=9Hz) ; 3. 7 (5H, m) ; 3. 6 (2H, m) ; 3. 1 (4H, t, J=1. 77 Hz) ; 2 (3H, s). 24. </| H | H | Mol. Wt | Yield 24. H H Mol. Wt Yield 466 80% 7. 6 (lH, d, J=15. 4 Hz), 7. 5 (2H, m), 7. 4 (1H, dd, J=2. 52 Hz), 7. 38 (3H, m), 7. 0 (lH, dd, J=1. 86 Hz), 6. 9 (1H, m), 6. 0 (1H, t), 4. 8 (1H, m), 4. 0 (1H, t, J=8. 94 Hz), 3. 9 (4H, d), 3. 6 (3H, m), 3. 0 (4H, t, J=4. 6 Hz), 2. 0 (3H, s). 25. AcOv H H Mol. Wt Yield Au 524 57% 7. 65 (1H, d, J=15. 4 Hz), 7. 5 (2H, d, J=8. 7 Hz), 7. 4 (lH, dd, J=2. 4&11. 7 Hz), 7. 1 (2H, d, J=8. 7 Hz) ; 7. 0 (1H, d, J=2. lHz) ; 6. 9 (1H, d, J=9Hz) ; 6. 8 (1H, d, J=15Hz) ; 6. 3 (lH, t, J=6. 3Hz) ; 4. 7 (m, 1H) ; 4 (1H, t, J=9Hz) ; 3. 8 (4H, m) ; 3. 09 (4H m) ; 2. 3 (3 H, s) ; 2. 0 3H, s. 26. H H Mol. Wt Yield a 472 60% 7. 49 (1H, dd, J=11. 64 Hz, 2. 46 Hz), 7. 09 (1H, dd, J=1. 65 Hz, 8. 73 Hz), 6. 8 (2H, m), 6. 2 (1H, dd, J=14. 1 Hz), 4. 79 (lH, m), 4. 02 (1H, t), 3. 9 (1H, t, J=8. 9 Hz), 3. 7 (7H, m), 3. 0 (4H, t, J=4. 7 Hz), 2. 02 (3H, s), 2. 1 (1H, m), 1. 7 (4H, m), 1. 19 (6H, m). 27. H H Mol. Wt Yield 511 55% cN 8. 2 (2H, d, J=8. 76 Hz), 7. 7 (3H, m), 7. 5 (2H, m), 7. 12 (2H, m), 6. 9 (lH, t, J=9. 1 Hz), 4. 8 (lH, m), 4. 0 (lH, t, J=9 Hz), 3. 8 (5H, m), 3. 6 (2H, t, J=5. 5 Hz), 3. 1 (4H, m), 1. 9 (2H, s). (solvent used is CDCl3+DMSO-d6) 28. H H Mol. Wt Yield Ace 582 81% OAc 7. 6 (lH, d, J=15. 3 Hz), 7. 45 (lH, dd, J=2. 7 & 11. 7 Hz), 7. 38 (1H, d), 7. 2 (1H, d, J=8. 1 Hz), 7. 09 (dd, J=2 & 6. 3 Hz), 6. 95 (1H, t, J=9 Hz), 6. 8 (1H, d, J=15. 3 Hz), 6. 1 (1H, t), 4. 76 (1H, m), 4. 04 (1H, t), 3. 75-3. 5 (3H, complex), 3. 07 (5g t), 2. 3 (7H, s), 2 (4H, s), 1. 65 (2H, s). 29. H H Mol. Wt Yield 481 6. 9% 7. 52- 7. 46 (2H, dd, J=2. 4, 2. 7 Hz), 7. 39-7. 34 (1H, d, J=15 Hz), 718- 7. 15 (lH, dd, J=2. 4, 2. 1 Hz), 6. 93- 6. 8 (lH, d, J=15 Hz), 6. 55- 6. 52 (2H, d, J=8. 4 Hz), 4. 69- 4. 6 (lH, m), 4. 10- 4. 04 (lH, t, J=9 Hz), 4-3. 66 (4H, t), 2. 95 (4H, b), 1. 81 (3H, s) (solvent used is DMSO- d6) 30. 8 H H Mõl. Wt Yield s I 494 40% 8. 22 (lH, t), 8. 04- 8. 01 (2H, t, J=7. 2 Hz), 7. 81- 7. 76 (lH, d, J=15. 3 Hz), 7. 59-7. 54 (2H, t, J=7. 2 Hz), 7. 51- 7. 46 (2H, dd, J=2. 4 Hz), 7. 50 - 7. 45 (lH, d, J=15. 3 Hz), 7. 16- 7. 15 (lH, d, J=2. 1 Hz), 4. 69 (lH, m), 4. 10-4. 04 (lH, t, J=8. 7, 9 Hz), 3. 71 (4H, b), 3. 0 (4H, b), 1. 81 (3H, s). (solvent used is DMSO-d6) 31. H H Mol. Wt Yield AcHX 551 12% AcH 8. 03 (1H, d) ; 7. 81 (1H, d) ; 7. 52 (1 H, d) ; 7. 47 (lH, d) ; 7. 19 (lH, d) ; 7. 1 (1 H, t) ; 4. 71 (1H, m) ; 4. 1 (1H, t) ; 3. 73 (4 H, m) ; 3. 23 (4 H, m) ; 2. 02 (3 H, s) ; 1. 82 3H, s. solvent used is DMSO-d6) 32. o H H Mol. Wt Yield 524 13% Met 8. 06 (2H, d, J=8. 7 Hz), 8. 03 (lH, d, J=14 Hz), 7. 53 (lH, d, J=14Hz), 7. 5 (lH, dd, J=2. 4 & 10 Hz), 7. 1 (lH, dd, J=2 & 6Hz), 6. 98 (2H, d, J=9. 2 Hz), 6. 92 (1H, t, J=9. 2 Hz), 5. 9 (IH, t, J=6 Hz), 4. 7 (1H, m), 4. 02 (1H, t, J=9 Hz), 3. 81 (3H, t), 3. 1 (5H, t), 2. 1 (4H, t), 1. 52 6 H, s 33. H H Mol. Wt eld lu 523 27% ACHE 7. 60-7. 65 (1H, d, J=15. 6 Hz), 7. 46-7. 52 (3H, complex), 7. 06-7. 10 (1H, dd, J=2. 1, 6. 6 Hz), 6. 83-6. 88 (1H, d, J=15. 3 Hz), 4. 7 (1H, m), 3. 98-4. 0 (1H, t, J=9 Hz), 3. 08 (4H, s), 2. 1 (3H, s), 1. 98 (3H, s). (solvent used is CDC13+DMSO-d6) 34. H H Mol. Wt Yield 544 21% i i (lH, d, J=8. 1 Hz), 8. 1 (1H, d, J=8. 4 Hz), 7. 9 (1H, d, J=8. 1 Hz) 7. 72 (lH, ddd, J=7. 2 Hz), 7. 62 (1H, dd, J=6. 9 Hz), 7. 52 (lH, d, J=8. 1 Hz), 7. 5 (1H, dd, J=2 & 9. 8 Hz), 3. 9 (4H, b. s.), 3. 7 (9. 1 H,), 3. 6 (1H, complex), 3. 39 (2H, s), 3. 08 (2H, b), 2. 6 (6H, s) 7. 1 (1H, dd, J=2 Hz & 7. 2 Hz), 7 (1H, t), 4. 7 (lem) ; 4. 6 (9. 1 H), 4. 05 (lH, t), . 2. 01 (3H, s) 35. n H H Mol. Wt Yield ON 0 501 40% 7. 5 (1H, d, J=15. 3Hz) ; 7. 4 (lH, d, J=14. 1 Hz) ; 7. 36 (1H, d, J=3. 73 Hz), 7. 10 (1H, d, J=8. 7 Hz) ; 6. 9 (1H, t, J=9Hz), 6. 7 (1H, d, J=3. 6Hz) 4. 7 (1H, m) (lH, t, J=9Hz) ; 3. 7 (4 H, m) ; 3. 1 (4 H, m) ; 2. 02 (3H, s). 36. H H Mol. Wt Yield 0 486 41% -0-"486 41% 7. 48 (1H, dd, J=17. 04 Hz) ; 7. 42 (lH, d, J=15. 05 Hz) ; 7. 08 (1H, dd, J=9. 1 Hz) ; 6. 93 (lH, t, J=6. 02 Hz) ; 6. 84 (lH, d, J=15 Hz) ; 6. 51 (lH, d) ; 6. 35 (lH, d, J=9. lHz) ; 4. 76 (lH, m) ; 4. 64 (2H, s) ; 4. 05 ( 1 H, t, J=6 Hz) ; 3. 88 (2H, m) ; 3. 82 (1H, m) ; 3. 76 (4H, m) ; 3. 06 (4H, m). 37. 0 H H Mol. Wt Yield H3C 432 33% HsC 7. 49 (1H, dd, J=2 Hz & 11. 6 Hz), 7. 2 (lH, d, J=16 Hz), 7. 1 (lH, dd, J=2 & 7. 5 Hz), 6. 9 (1H, t, J=9. 06 Hz), 4. 78 (1H, m), 4. 05 (1H, t), 3. 7 (3H, t), 7. 06 (1H, d, J=15. 36 Hz), 6. 3, (1H, t) 3. 89 (2H, t), 3. 6 2H, complex (solvent used is DMSO-d6) 38. H H Mol. Wt Yield 544 31% MEONS 8. 01 (2H, d, J=8. 51 Hz), 7. 94 (2H, d, J=8. 48 Hz), 7. 61 (1H, d, J=15. 43 Hz), 7. 52 (1H, d, J=15. 43 Hz), 7. 47 (1H, dd, J=17. 31 Hz), 7. 19 (1H, d, J=11. 16 Hz), 7. 11 (1H, t, J=6. 15 Hz) 4. 72 (1H, m), 4. 10 (1H, t, J=5. 98 Hz), 3. 88 (2H, m), 3. 73 (4H, m), 3. 40 (2H, m), 3. 31 (3H, s) 3. 0 (4 H, m), 2. 02 3H, s). (solvent used is DMSO-d6) 39. o H H Mol. Wt Yield eJk 572 45% Br 7. 9 (3H, t), 7. 6 (2H, d, J=8. 58 Hz), 7. 5 (1H, d, J=14. 9 Hz), 4 (1H, dd, J=11. 64, 2. 52 Hz), 7. 0 (1H, dd, J=6. 9, 1. 8 Hz), 6. 9 (1H, t, J = 9 Hz), 5. 9 (1H, t), 4. 7 (1H, m), 4. 0 (1H, t, J=9 Hz), 3. 9 (2H, t), 3. 8 (2H, t), 3. 63H, m, 3. 04H, t, J =4. 9 Hz), 2. 0 (3X s). 40. (H3Cl3C H H Mol. Wt Yield 594 40% HOLZ C (CH3) 3 7. 6 (1H, d, J=15. 3 Hz), 7. 4 (1H, dd, J=2. 4 & 11. 7 Hz), 7. 3 (3H, s), 7 (1H, dd, J=2. 1 & 6. 9 Hz), 6. 8 (1H, t, J= 9 Hz), 6. 7 (1H, d, J=15, 5. 4 Hz), (1 H, s), 4. 7 (1 H, m), 3. 9 (lH, t, J=10. 2 Hz) ; 3. 8 (4H, br), 3. 6-3. 7 (3H, complex), 3 (4 H, br), 2 (3 H, s), 1. 46 ( 18H, s). 41. Ac H H Mol. Wt Yield R-, Fcrl 528 55% 7. 5 (2H, t, J=2. 55 Hz), 7. 4 (1H, t, J=2. 55 Hz), 7. 0 (1H, dd, J=1. 86, 6. 9 Hz), 6. 9 (1H, t, J=9. 0 Hz), 6. 8 (1H, d, J=15 Hz), 6. 4 (2H, dd, J=3. 3 Hz), 6. 0 (1H, m), 5. 0 (2H, s), 4. 7 (1H, m), 2. 1 (3H, s), 2. 0 (3H, s). 42. Mol Wt Yield Me 470 33% 7. 48 (1H, dd, J=2. 52 Hz), 7. 45 (2H, d, J=15 Hz), 7. 0 (1H, d, J=3. 18 Hz), 6. 9 (1H, t, J=9. 1 Hz), 6. 7 (1H, d, J=14. 9 Hz), 6. 4 (1H, d, J=3. 18 Hz), 6. 0 (2H, q), 4. 7 (1H, m), 4. 0 (1H, t, J=9 Hz), 3. 8 (4H, s), 3. 6 (3H, m), 3. 0 (4H, t), 2. 3 (3H, s), 2. 0 H, s. 43./H H Mol. Wt Yield 467 54 % N 8. 6 (1H, d, J=4 Hz), 7. 6 (3H, m), 7. 3 (lH, d, J=7. 7 Hz), 6. 9 (1H, t, J=9 Hz), 7. 0 (1H, dd, J=2, 11. 6 Hz), 7. 4 (1H, dd, J=2. 52, 11. 6 Hz), 6. 0 (1H, t), 4. 7 (lH, m), 4. 0 (1H, t, J=9 Hz), 3. 9 (4H, t, J=6. 78 Hz), 3. 7 (3H, m), 3. 0 ( t, J=5 Hz), 2. 0 (H, s. (solvent used is DMSO-d6) 44.--Mol. Wt. Yield 0-464 T57, 97% 7. 5 (2H, t, J=6. 57 Hz), 7. 4 (3H, m), 7. 0 (1H, dd, J=1. 9, 8. 7 Hz), 6. 9 (1H, t), 6. 5 (lH, t) 4. 7 (2H, m), 4. 0 (3H, t, J=4. 4Hz), 3. 8 (2H, t J=5. 0 Hz), 3. 6 3H, m), 2. 0 (3H, s) 45. H H {NH. HCI Mol. Wt. Yield 455 80% 7. 49 (lH, dd, J=16. 74Hz), 7. 06 (lH, dd, J=10. 1 Hz), 6. 95 (lH, t, J=6. 0 Hz), 6. 91 (lH, m), 6. 75 (1H, d, J=12. 6 Hz), 6. 44 (lH, m), 6. 23 (lH, m), 5. 84 (1H, d, J=12. 57 Hz), 4. 9 (lH, m), 4. 02 (1H, t, J=6. 1 Hz), 3. 80 (4H, m), 3. 75 (2H, m), 3. 62 (1H, m), 3. 07 (4H, m), 2. 02 (3H, s) 46. Rq NH | H | H | Mol. Wt. | Yield H H Mol. Wt. 455 90% 11. 3 (br, 1H), 8. 24 (1H, t, J=11. 43 Hz), 7. 52 (1H, dd), 7. 38 (1H, d, J=15. 21 Hz), 7. 1 (1H, dd, J=2, 9. 3Hz), 6. 9 (1H, d, J=15. 21 Hz), 6. 1 (1H, br), 4. 7 (1H, m), 4. 0 (1H, t, J=9. 15, 9 Hz), 3. 7 (4H, m), 3. 31 (4H, m), 1. 8 3H, m solvent used is DMSO-d6) > o 47.-COOH H H Mol. Wt. Yield 434 38% 12. 9 (br, lH), 8. 23 (lH, t),. 51 (lH, dd, J=14. 32, 2. 37Hz), 7. 47 (lH, dd), 7. 43 (lH, d, J=15. 39Hz), 7. 09 (lH, t), 6. 54 (lH, d, J=15. 36Hz), 4. 71 (lH, m), 4. 10 (lH, t), 3. 69 (bs, 4H), 3. 4 (4H, m), 1. 81 (3H, s). (solvent used is DMSO-d6) 48. CN H Mol. Wt. Yield 491 32% 7. 8 (lH, dd, J=2. 1, 1. 2 Hz), 7. 4 (4H, m), 7. 0 (lH, dd, J=1. 8Hz), 4. 0 lH, t), 3. 8 (4H, m), 3. 6 3H, m, 3. 1 (4H, br, 2. 02 (3H, s). 49. < H H Mol. Wt. Yield J ! J 491 60% NCS 8. 22 (lH, br), 7. 85 (2H, d, J=8. 46Hz), 7. 51 (lH, dd, J=17. 19Hz), 7. 40 (lH, d, J=15. 27Hz), 7. 46 (2H, d, J=8. 46), 7. 18 ( lH, dd, 11. l), 7. 10 (lH, d, J=15. 27), 7. 05 (lH, t, J=6. 15), 4. 69 (lH, m), 4. 04 (lH, t, J=5. 99), 3. 71 (4H, m.), 3. 68 (lH, m), 3. 40 (2H, m), 2. 99 (4H, m), 1. 81 (3H, s). (solvent used is DMSO-d6) 50. H H Mol. Wt. Yield /517 22 % 02N S 8. 0 (lH, d, J=4. 3), 7. 7 (lH, d, J=15. 2), 7. 5 (lH, dd, J=11. 7, 2. 5), 6. 9 (2H, m), 5. 9 (lH, m), 4. 7 (lH, m), 3. 9 (lH, t, J=9), 3. 8 (2H, s), 3. 75H, m, 3. 14H, s"2. 03H, s. 51. C02Me Mol. Wt. Yield / 524 70% 7. 76 (lH, s), 7. 55 (lH, dd, J=16. 3), 7. 39 (5H, m), 7. 26 (lH, dd, J=10), 6. 77 (lH, t, J=5. 98), 6. 15 (lH, br), 4. 81 (lH, m), 4. 02 (lH, t, J=5. 98), 3. 99 (lH, m), 3. 93 (4H, m), 3 : 39 (4H, m), 3. 07 (2H, m), 2. 96 (3H, s), 2. 04 (3H, s). 52. w COOH H Mol. Wt. Yield tJ 510 60% 8. 22 (lH, bs), 2. 99 (4H, m), 7. 5 (lH, s), 7. 48 (1H, J=16. 3), 7. 39 (5H, m), 7. 13 (lH, dd, J=10), 6. 92 (lH, t, J=5. 98), 4. 81 (lH, m), 4. 04 (lH, t, J=5. 98), 3. 99 (lH, m), 3. 83 (4H, m), 3. 39 (4H, m), 3. 07 (2H, m), 2. 043H, s). (solvent used is DMSO-d6) 53. Q COOMe H Mol. Wt. Yield (n3l 514 35% 0 7. 53 (lH, s), 7. 5 (lH, d, J=3. 5), 7. 46 (lH, dd, J=16. 27), 7. 06 (lH, dd, J=11. 21), 6. 92 (lH, t, J=6. 05), 6. 76 (lH, t, J=6. 05), 6. 51 (lH, m), 6. 04 (lH, bs), 4. 07 (lH, m), 4. 04 (lH, t, J=5. 98), 3. 77 (4H, m), 3. 71 (3H, m), 3. 62 (lH, m), 3. 60 (2H, m), 3. 12 (4H, m), 2. 01 (3H, s). 54./r COOH H Mol. Wt. Yield 500 31% 8. 26 (lH, br), 7. 81 (lH, s), 7. 5 (lH, dd, J=17. 16), 7. 22 (lH, m), 7. 16 (lH, dd, J=17. 16), 7. 06 (lH, dd, J=11. 5), 6. 76 (lH, d, J=3. 48), 6. 59 (lH, m), 6. 04 (lH, bs), 4. 68 (lH, m), 4. 05 (lH, t, J=5. 59), 3. 77 (4H, m), 3. 62 (lH, m), 3. 39 (2H, m), 3. 0 (4H, m). (solvent used is DMSO-d6) 55. coome H Mol. Wt. Yield 02N 559 47% 8. 24 (bs, lH), 7. 76 (lH, d, J=3. 87), 7. 45 (lH, dd, J=17. 25), 7. 29 (lH, dd, J=3. 94), 7. 17 (lH, dd, J=11. 09), 7. 0491H, t, J=6. 19), 4. 71 (lH, m), 4. 09 (lH, t, J=5. 99), 3. 79 (4H, m), 3. 65 (lH, m), 3. 44 (2H, m), 3. 32 (3H, s), 2. 86 (4H, m), 1. 81 (3H, s). (solvent used is DMSO-d6) 56. COOH H Mol. Wt. Yield 02N- 545 62% 8. 98 (lH, bs), 8. 23 (lH, s), 7. 76 (lH, d, J=3. 87), 7. 45 (lH, dd, J=17. 17), 7. 22 (lH, d, J=3. 94), 7. 17 (lH, dd, J=11. 09), 7. 04 (lH, t, J=8. 19), 4. 71 (lH, m), 4. 99 (lH, t, J=5. 99), 3. 79 (4H, m), 3. 65 (lH, m), 3. 44 (2H, m), 2. (4Km), 1. 81 (3H, s). (solvent used is DMSO-d6) Preparation 2

(S)-N- (3- {3-Fluoro-4- [4- (6-methoxy-l-oxo-1, 2,3, 4-tetrahydronapthalen-2-yl methyl)- piperazin-1-yl]-phenyl]-2-oxo-oxazolidin-5-yl methyl) acetamide (Compound No. 61)

A cold solution of (S)-N- [ [3- [3-fluoro-4- (N-1-piperazinyl)-phenyl]-2-oxo-5- oxazolidinyl] methyl acetamide (0. 17 g) in methanol (5 ml) was added gradually to a stirred, cold solution of 37 % aq. Formaldehyde (2 ml) in methanol (5 ml). The reaction mixture was kept in a freezing mixture of ice-salt (-10 °C to-15 °C) for 1 hour. The solvents were removed in vacuum and the residue was dissolved in methanol (5 ml). The resulting solution was cooled in a freezing mixture and a solution of dry HCl (g) in diethyl ether was added. The solvents were removed in vacuum and a solution of 6- methoxy-a-tetralone (0. 039 g) in methanol (2 ml) was added to the resulting mass. The reaction mixture was heated on a water bath for 15-20 minutes. The solid separated was filtered to afford a sticky solid which was chromatographed on silica gel with 0-3 % MeOH/CHCl3 gradient to give the title compound as a white solid (50 mg, 18 %).

The following compounds were prepared following a similar procedure as described above: Table 2: 57. Mol. Wt. Yield (%) A o Mol. Wt. Yield MeO 524. 58 29% 7. 98 (lH, d, J-8. 8Hz), 7. 61 (1 H, d, J=10. 8Hz), 6. 85 (1H ; d, J=7. 59Hz), 4. 78 (lH, m) ; 3. 8 (3H, s), 2. 04 (3H, s), 6. 03 (lH, m) ; 3. 0 (4H, broad d) ; 3. 4 (4H, complex) ; 7, (2H, bs) ; 1. 23 (4H, complex), 1. 5 (16H, br) 58. o Mol. Wt Yield 494. 56 20% 7. 95 (lH ; dd, J=1. 5 & 6. 8Hz), 7. 5 (2H, m), 7. 32 (2H, t), 7. 14 ( lH ; dd, J=2. 1 & 8Hz) ; 7. 08 (lH ; t, 9=9. 1 Hz), 4. 8 (2H, m), 4. 1 ( lH, t), 3. 78 (1H, quart), 3. 55 (2H, d), 2. 6 (3H, m), 2. 6 (3H, m), 3. 08 (7H, m), 1. 9 (4H, complex), 4. 6 (lH, s) (solvent used is CD30D) 59. o Mol. Wt Yield MeO 510. 56 20% Mu0 7. 69 (lH ; dd, J=7. 89 Hz), 7. 54 (lH ; d, J=12. 6H) ; 6. 94 (lH ; d, J=7. 8 Hz), 6. 43 (lH, m), 4. 8 (lH, m), 3. 8 (3H, 3), 3. 4 (7H, complex), 3. 3 (8H, complex), 7. 0 (3H, t), 1. 73 (3H, bs), 4. 02 (2H, s) 60. o Mol. Wt Yield cl 446. 5 22% 7. 5 (lH, d), 6. 9 (2H, t), 4. 7 (lH, m), 2. 01 (3H, s), 3. 4 (2H, t), 2. 03 (3H, s), 4. 03 (1H, t), 3. 8 (complex), 3. 37 (4H, complex), 3. 14 (1H, bs,), 2. 5 (2H, bs), 1. 37 (6H, t) 61. not Mol. Wt Yield Meoll 540 59% 7. 44 (1H ; dd, J=2. 4 & 11. 6 Hz), 7. 07 (1H ; dd, J=2. 1 & 6. 78Hz), 6. 95 (lH ; t, J=9. 09Hz), 4. 84 (lH, m), 3. 35 (4H, t), 3. 10 (4H, t), (3H, s), 3. 7 (5H, m), 3. 71 (2H, s), 1. 5 (2H, complex) ( the solvent used is CDC13+CD30D) 62. 0 Mol. Wt Yield 508. 5 12% Me 8. 02 (lH, d J=8. 76Hz), 7. 75 (lH ; t, J=2. 5 & 11. 6 Hz), 7. 04 ( lH ; dd, J=2. 2 & 6. 8 Hz), 6. 9 (lH ; t, J=9. 12 Hz) ; 6. 84 (1H ; dd, J=2. 49 & 6. 27 Hz), 6. 7 (1H, d, J=2. 37 Hz), 4. 8 (lH, m), 4. 3 (1H, dd), 2. 37 lH, m) Preparation 3

(S)-N- [3- {4- (4- (3-Benzo [1, 3]-dioxol-5-yl acryloyl)-piperazin-1-yl]-3-fluorophenyl]-2- oxo-oxazolidin-5-yl methyl] thioacetamide (Compound No. 63)

A stirred suspension of (S)-N- [ [3-Fluoro-4- (N-1-piperazinyl)-phenyl]-2-oxo5- oxazolidinyl] methyl acetamide (0.2 g) in toluene (25 ml) was treated with Lawesson's reagent (0.24 g) under nitrogen atmosphere and refluxed for 5 hrs (TLC). The solvents were evaporated and the residue was chromatographed on silica gel using eluent 0-1% methanolic ammonia/CH2C12. The resulting solution was concentrated and was taken as such for reaction.

(S)-N-[[3-Fluoro-4-(N-1-piperzinyl)-phenyl]-2-oxo5-oxazol idinyl] methyl thioacetamide prepared as above (0.2 g) was taken in dichlormethane (50 ml). To this solution was added HOBt. H20 (0.2 g) and 1- (3-Dimethylaminopropyl)-3- ethylcarbodiimide hydrochloride (0.2 g) followed by 3,4-methylene dioxycinnamic acid (0.109 g). The reaction mixture was stirred at ca 27 °C to which triethylamine (1 ml) was added. The reaction mixture was stirred for 3 hrs at 27 °C [TLC]. The reaction mixture was washed with DM water, organic layer was separated and dried over anhydrous sodium sulfate and solvents were evaporated. The resulting residue was chromatographed over silica gel with mobile phase 0-5% methanol/CH2Cl2. The resulting solution was concentrated to afford the title compound (0.1 g, 33%).

The following compounds were prepared according to the above procedure.

Table 3: 63. Z R4 R3 Mol. Wt. Yield I o H H 526 31% 7. 41-7. 46 (lH, d, J=15. 6Hz), 7. 05-7. 19 (4H, complex), 6. 09 (lH, d), 6. 05 (2H, s), 4. 9 (1H, m), 4. 09-4. 15 (1H, t, J=9. 0, 9. 3 Hz), 3. 8 (4H, b), 2. 97 (4H, b), 2. 42 (3H, s) (the solvent used is DMSO-d6) 64. Mol. Wt Yield HO H H 498 78% 7. 6 (lH, d, J=15. 33 Hz), 7. 4 (3H, t), 7. 1 (1H, d, J=8. 82 Hz), 6. 9 (1H, t, J=9. 0 Hz), 6. 8 (2H, d, J=8. 52 Hz), 6. 7 (1H, d, J=15. 36 Hz), 4. 9 (1H, 2), 4. 1 (3H, m), 3. 1 (s, 4H), 2. 5 (s, 3H). (the solvent used is CDCl3+drops of CD30D) 65. H H Mol. wt Yield ire 483 43% N 8. 7 (1H, d, J=1. 74 Hz), 8. 5 (2H, 2, J=1. 44 Hz), 7. 8 (1H, d), 7. 7 (1H, d, J=15. 54Hz), 7. 5 (1H, q, J=2. 5 m, 11. 73 Hz), 7. 0 (2H, m), 5. 0 (1H, m), 3. 8 (8H, m), 3. 1 (4H, t), 2. 5 (5H, 2). (the solvent used is CDC13+drops of CD30D) 66./ruz H H Mol. Wt Yield 4 472 62% 7. 7 (1H, 3), 7. 4 (2H, m), 7. 0 (1H, dd, J=2. 22 Hz), 6. 9 (1H, t), 6. 8 (1H, d, J=15. 0 Hz), 6. 5 (1H, d, J=3. 36 Hz), 6. 4 (1H, q, J=1. 86 Hz), 4. 9 (1H, m), 4. 2 (2H, m), 4. 0 (8H, m), 3. 0 (4H, t, J=4. 45 Hz), 2. 6 (3H, s). 67. F/H H Mol. Wt Yield F 518 68% F 7. 6 (1H, d, J=15. 42 Hz), 7. 48 (1H, dd, J=2. 52 Hz), 11. 58 Hz), 7. 1 (2H, m), 7. 0 (1H, q, J=1. 83 Hz), 6. 8 (2H, d, J=15. 36 Hz), 4. 3 (1H, m), 4. 0 (7H, m), 3. 4 (1H, s), 3. 1 (4H, s), 2. 6 (3H, s) (the solvent used is CDC13+drops of CD30D) 68. H H Mol. Wt Yield 500 49% 7. 7 (1H, d, J=15. 42 Hz), 7. 5 (2H, m), 7. 1 (3H, m), 6. 8 (1H, d, J=15. 39 Hz), 6. 9 (1H, t, J=9. 0 Hz), (1H, m), 4. 2 (1H, m), 4. 0 (2H, m), 3. 8 (5H, complex), 3. 0 (4H, t, J=4. 4 Hz), 2. 6 (3H, s) 69. H H Mol. Wt Yield OH 498 9% OH 7. 47-7. 53 (1H, dd, J=2. 4 Hz), (lH, dd, J=2. 4 Hz), 7. 38-7. 43 (lH, d, J=15. 4 Hz), 7. 19-7. 21 (1H, t, J=4. 2, 3. 6 Hz), 7. 11-7. 16 (lH, d, J=14. 7 Hz), 6. 76-6. 79 (lH, dd), 4. 92 (lH, m), 4. 12 (H, t), 3. 77-3. 9 (3H, complex), 3. 72-3. 75 (4H, b. t,), 2. 98 (4H, b. t), 2. 4 ( 3H, s). (the solvent used is DMSO-d6) 70. H H Mol. Wt 488 170% 2. 60 (3H, s), 3. 08 (4H, m), 3. 87 (4H, m), 4. 02 (1H, m), 4. 07 (H, m), 4. 11 (1H, t, J=4. 5 Hz), 4. 99 (1H, m), 6. 68 (1H, d, J=15. 06 Hz), 6. 95 (1H, t, J=4. 56Hz), 7. 06 (1H, t, J=6. 1 Hz), 7. 22 (lH, dd, J=10. 8 Hz), 7. 24 (lH, d, J=3. 4 Hz), 7. 32 (lH, d, J=5 Hz), 7. 42 (1H, dd, J=16. 5 Hz), 7. 81 (lH, d, J=15 Hz), 7.. 96 (lH, br) 71. H H Mol. Wt Yield H 521 31 % OWN H 10. 35 (1H, s), 8. 3 (lH, d), 7. 8 (lH, d, J=2. 4 Hz), 7. 75 (lH, d), 7. 4 (lH, d, J=6. 9 Hz), 7. 1 (5H, complex), 4. 9 (1 H, m), 3. 8 (lH, t), 3. 7 (4H, bt), 3. 0 (4H, t), 2. 4 (3H, s). (the solvent used is DMSO- d6) 72. I H H Mol. Wt Yield NoS l 483 27% 8. 7 (1H, d, J=1. 74 Hz), 8. 5 (2H, 2, J=1. 44 Hz), 7. 8 (1H, d), 7. 7 (1H, d, J=15. 54 Hz), 7. 5 (1H, q, J=2. 5 Hz, 11. 73 Hz), 7. 0 (2H, m), 5. 0 (1H, m), 3. 8 (8H, m), 3. 1 (4H, t), 2. 5 (5H, s). 73. H H Mol. Wt Yield H2N" 497 8% Han 7. 61-7. 78 (lH, d, J=15 Hz), 7. 47-7. 48 (1H, dd, J=2. 7 Hz), 7. 35- 7. 38 (1H, d, J=8. 4 Hz), 7. 05-7. 08 (1H, dd, J=1. 8, 6. 9 Hz), 6. 89- 6. 95 (lH, t, J=9 Hz), 6. 64-6. 67 (1H, d, J=8. 7 Hz), 4. 9 (lH, m), 4. 0-4. 1 (3H, complex), 3. 8 (4H, br), 3. 0 (3H, t), 2. 5 (3H, s). (the solvent used is DMSO-d6) 74. H H Mol. Wt Yield 482 79% 2. 56 (3H, s), 3. 07-3. 10 (4H, m), 3. 78-3. 83 (4H, m), 4. 04-4. 01 ( lH, m), 4. 10 (2H, m), 4. 25 (lH, t, J=5. 9 Hz), 4. 97 (lH, m), 6. 88- 6. 93 (lH, t, J=4. 48 Hz), 6. 95-6. 88 (1H, d, J=13. 23 Hz), 7. 05 ( lH, dd, J=10 Hz) 7. 37-7. 38 (5H, m), 7. 52 (lH, dd, J=15. 42 Hz), 7. 67-7. 73 (1H, d, J=15. 42 ho, 7. 90 (lH, bs) 75. H H | Mol. Wt Yield Meo I -512 80% (3H, S) 2. 68 (3H, S) 3. 08 (4H, m) 3. 84 (4H, m), 4. 01 (1H, m), 4. 06 (2H, m), 4. 10 (lH, t, J=4. 35 Hz), 5. 0 (lH, m), 6. 83 (1H, d, J=15. 33 Hz), 6. 92 (2H, d, J=9 Hz), 6. 97 (lH, t, J=6. 1 Hz), 7. 09 (lH, dd, J=10. 62 Hz), 7. 42-7. 47 (1H, dd, J=16. 2 Hz), 7. 51 (2H, d, J=8. 52 Hz), 7. 61 (lH, d, J=15. 33 Hz), 10 (lH, br) (the solvent used is CDC13 drop of DMSO-d6) 76. < H H Mol. Wt Yield Aco'54063% 7. 76-7. 79 (2H, d, J-8. 4Hz), 7. 52-7. 54 (lH, t, J=2. 4Hz), 7. 47-7. 49 (lH, d, J=4. 2Hz), 7. 25-7. 30 (lH, d, J=15. 6 Hz), 7. 19-7. 20 (lH, d, J=2. 4Hz), 7. 14-7. 19 (1H, d,, J=15 Hz), 7. 12-7. 14 (JH, d, J=8. 4 Hz), 4. 88-4. 94 (lH, m), 4. 09-4. 15 (lH, t, J= 9 Hz), 3. 7 (4Rb), 2. 9 (4H, br), 2. 4 (3H, s), 2. 2 (3H, s). (the solvent used is DMSO-d6) 77. H H Mol. Wt Yield MeOJX 540 15% Me0'v 8. 06 (2H, d, J=2. 2 Hz), 7. 9-8. 0 (lH, d, J=15. 9 Hz), 7. 49-7. 53 (lH, d, J=12 Hz), 7. 44-7. 49 (1H, dd, J=2. 7 Hz), 7. 06-7. 07 (lH, d, J=1. 8 Hz), 4. 9 (lH, m), 3. 87-3. 92 (4H, t, J=6. 6 Hz), 3. 07-3. 11 (4H, t, J=5. 1 Hz), 2. 6 (3H, s), 5. 0 (solvent used is DMSO-d6) 78. m | H H Mol. Wt Yield Meo2so 576 40% 7. 6 (1H, d, J=15. 33 Hz), 7. 4 (3H, t), 7. 1 (1H, d, J=8. 82 Hz), 6. 9 (1H, t, J=9. 0 Hz), 6. 8 (2H, d, J=8. 52 Hz), 6. 7 (1H, d, J=15. 36 Hz), 4. 9 lH, s, 4. 1 (3), 3. 1 4H, s, 3. 0 3H, s 2. 5 (3H, s). 79. S H | H Mol. Wt Yield 02N o l 517 36% 7. 4 (2H, m), 7. 3 (2H, q, J=3. 78 Hz), 6. 9 (2H, t, J=9 Hz), 6. 7 (2H, d, J=3. 78 Hz), 7. 0 (1H, dd, J=1. 8, 6. 9 Hz), 4. 9 (lH, m), 4. 5 (2H, s), 4. 0 (4H, m), 3. 8 (lH, m), 2. 6 (4H, br), 2. 6 (3H, s). 80. Mol. Wt. Yield \/480 44% 7. 57 (2H, dd, J=1. 4, 6. 51Hz), 7. 42 (4H, m), 7. 0 (1H, dd, J=8. 7 &1. 9Hz), 6. 9 (1H, t, J=9Hz), 4. 9 (lH, m), 4. 3 (lH, m), 4. 08 (2H, t, J=8. 85Hz), 4. 01 (1H, t, J=5. 3Hz), 3. 8 (m, 3H), 3. 1 (2H, t, J=5. 0Hz), 3. 0 (2H, t, J=5. 0Hz), 2. 6 (3H, s) Preparation 4

(S)-N- [3- (3-fluoro-4- {4- [3- (thiophen-2-yl)-acryloyl]-piperazinyl]-phenyl)-2-oxo- oxazolidin-5-yl-methyl alcohol (Compound No. 81) To a solution of (S)-N- [ [3- [3-fluoro-4- (N-piperazinyl)]-phenyl]-2-oxo-5- oxazolidinyl] methyl alcohol (2 g) in dichloromethane (50 ml) was added HOBt. H20 (1.0 g), 1- (3-Dimethyl aminopropyl) -3-ethyl carbodiimide hydrochloride (1.0 g) followed by 3- (2-thienyl) acrylic acid (1.04 g). The reaction mixture was stirred at ca. 27 °C to which triethylamine (4ml) was added.

After stirring for 2 hrs. at ca. 27 °C (TLC) the reaction mixture was filtered to give white cake and cake was washed with chilled dichloromethane (20 ml) to afford the title compound (2.13g, 73%) m. p. 230-235 °C.

The following compounds were prepared following the above procedure.

Table 4: 81. Z R4 R3 H H Mol. Wt. Yield 431431/o 7. 7 (1H, d, J=15. 06 Hz), 7. 5 (lH, dd, J=2. 4, 12. 6 Hz), 7. 4 (1H, d, J=3. 6 Hz), 7. 11 (1H, dd, J=3. 6, 1. 5 Hz), 7. 0 (lH, d, J=9Hz), 6. 9 (1H, d, J=15Hz), 4. 6 (lH, m), 4. 0 (1H, t, J=9Hz), 3. 7 (4H, m), 2. 9 (4H, brs). (the solvent used was DMSO-d6) 82. H H Mol. Wt Yield 483 86% 7. 76 (1H, d, J=8. 28 Hz), 7. 56 (1H, dd, J=17. 37 Hz), 7. 49 (1H, d, J=15. 43 Hz), 7. 21 (1H, dd, J=10. 12 Hz), 7. 17 (1H, d, J=15. 43 Hz), 7. 07 (1H, t, J=6. 1Hz), 6. 76 (2H, d, J=8. 28 Hz), 5. 20 (lH, br), 4. 06 (1H, t, J=5. 98 Hz), 3. 81 (4H, m), 3. 76 (2H, m), 3. 63 (lH, m), 3. 03 (4H, m), 2. 26 (3H, s) (the solvent used was DMSO-d6) 83. H H Mol. Wt Yield 450 85% 450 85% 7. 56 (1H, dd,, J=17. 34 Hz), 7. 48 (lH, m), 7. 4 (1H, d, J=15. 24 Hz), 7. 19 (2H, m), 7. 18 (1H, dd, J=10. 34 Hz), 7. 16 (1H, t, J=6. 2 Hz), 7. 13 (1H, d, J=9. 15 Hz), 7. 07 (1H, d, J=15. 24 Hz), 6. 94 (1H, d, J=7. 98 Hz), 6. 05 (2H, s), 4. 82 (lH, m), 4. 03 (1H, t, J=6. 01 Hz), 3. 85 (2H, m), 3. 78 (4H, m), 3. 68 (lH, m), 2. 97 (4H, m). (the solvent used was DMSO-d6 84. H H Mol. Wt Yield 464 95% zon H 10. 71 (1H, s)., 7. 98 (1H, d, J=15. 27 Hz), 7. 57 (1H, dd, J=17. 34 Hz), 7. 47 (lH, m), 7. 44 (2H, m), 7. 22 (2H, m), 7. 10 (1H, dd, J=10. 80 Hz), 7. 09 (1H, t, J=6. 39 Hz), 6. 88 (1H, d, J=15. 27 Hz), 4. 7 (lH, m), 4. 00 (1H, t, J=6. 15 Hz), 3. 90 (2H, m), 3. 84 (4H, m), 3. 70 (lH, m), 3. 10 (4H, m). (solvent used is CDC13 +DMSO) 85. H H Mol. Wt Yield 415 79% 7. 78 (1H, d, J=1. 2 Hz), 7. 55 (lH, dd, J = 17. 36 Hz), 7. 38 (1H, d, J=15. 19 Hz), 7. 18 (1H, dd, J=10. 74 Hz), 7. 09 (1H, t, J=6 Hz), 6. 97 (1H, d, J=15. 19 Hz), 6. 87 (1H, d, J=3. 31 Hz), 6. 60 (lH, m), 5. 21 (lH, br), 4. 80 (lH, m), 1. 06 (lH, t, J=5. 99 Hz), 3. 80 (4H, m), 3. 64 (2H, m), 3. 55 (1H, m), 2. 97 (4H, m) (the solvent used was DMSO-d6) 86. 1 H H Mol. Wt Yield 426 84% 8. 61 (2H, d, J=5. 88 Hz), 7. 70 (2H, d, J=6. 0 Hz), 7. 56 (1H, d, J=15. 40 Hz), 7. 50 (1H, dd, J=14. 90 Hz,), 7. 43 (1H, d, J=15. 40 Hz), 7. 22 (1H, dd, J=10. 84 Hz), 7. 04 (1H, t, J=6. 20 Hz), 5. 20 ( 1H, brs), 4. 68 (lH, m), 4. 06 (lH, t, J=5. 98 Hz), 3. 87 (2H, m), 3. 77 (4H, m), 3. 61 (lH, m), 2. 99 (4H, m) (the solvent used was DMSO-d6) 87. w H H Mol. Wt Yield 443 74% 8 7. 81 (1H, d, J=8. 7 Hz), 7. 56 (2H, d, J=8. 7 Hz), 7. 50 (1H, dd, J=17. 31 Hz), 7. 29 (2H, d, J=8. 7 Hz) 7. 27 (1H, dd, J=10. 11 Hz), 7. 21 (lH, d, J=14. 35 Hz), 7. 18 (1H, t, J=6. 31 Hz), 4. 82 (lH, m), 4. 03 (lH, t, J=6. 12 Hz), 3. 80 (2H, m), 3. 77 (4H, m), 3. 72 (lH, m), 2. 98 4H, m. the solvent used was DMSO-d6) 88. [< | | | Mol. Wt | Yield 88. H H Mol. Wt Yield 425 83% 7. 71 (1H, d, J=14. 71 Hz), 7. 54 (5H, m), 7. 50 (1H, dd, J=17. 05 Hz), 7. 38 (1H, d, J=14. 71 Hz), 7. 28 (1H, dd, J=10. 15 Hz), 7. 08 (1H, t, J=6. 19 Hz), 4. 8 (1H, m), 4. 03 (1H, t, J=6. 01 Hz), 3. 80 (2H, m), 3. 75 (1H, m), 3. 62 (4H, m), 2. 98 (4H, m) (the solvent used was DMSO-d6). 89. H H Mol. Wt Yield 455 86% MeO 7. 69 (1H, d, J=8. 74 Hz), 7. 55 (1H, dd, J=10. 7 Hz), 7. 45 (1H, d, J=15. 51 Hz), 7. 19 (1H, d, J=15. 51 Hz), 7. 18 (1H, dd, J=11. 77Hz), 7. 12 (IH, t, J=5. 28 Hz), 6. 94 (2H, d, J=8. 74 Hz), 4. 68 (lH, m), 4. 0 (1H, t, J=6. 68 Hz), 3. 84 (2g m), 3. 71 (1H, m), 3. 62 (4H, m), 3. 01 (4H, m). (the solvent used was DMSO-d6) Preparation 5

(S)-N- [3-fluoro-4- {4- [3- (thiophen-2-yl)-acryloyl]-piperazinyl]-phenyl]-2-oxo- oxazolidin-5-yl-methyl methano sulfonate (compound No. 90) (S)-N- [3- (3-Fluoro-4- {4- (3- (thiophen-2-yl)-acryloyl}-piperazinyl]-phenyl)-2-oxo- oxazolidin-5-yl-methyl alcohol (2g) was taken in pyridine (10ml) and dichloromethane (25 ml) to which was added triethylamine (10 ml). The reaction mixture was cooled to 5 °C and methane sulfonyl chloride (1.5 ml) was added slowly. The reaction mixture was stirred for 3 hrs. at 0-5°C (TLC). The reaction mixture was washed with DM water (50 ml). The organic layer was separated and dried over anhy. sodium sulfate. After evaporation of solvents the residue was titurated with diethyl ether to afford the title compound as brown solid (2.14 g, 90%) mp. 166-170 °C.

The following compounds prepared following the above procedure.

Table 5: Z R4 O # O<BR> R3 N N N<BR> O OSO2Me F 90. R R4 R3 Mol. Wt. Yield H H 509 90% zu 7. 8 (1H, d, J=15. 06 Hz), 7. 4 (1H, dd, J=2. 4, 11. 7 Hz), 7. 3 (1H, d, J=4. 8 Hz), 7. 2 (1H, d, J=3. 3 Hz), 7. 0 (1H, dd, J=9, 6 Hz), 6. 7 (1H, d, J=15. 06 Hz), 4. 9 (1H, m), 4. 1 (1H, t, J=9 Hz), 3. 8 (4H, m), 3. 15 (4H, m ), 3. 10 (3H, s). (the solvent used was DMSO-d6) 91. H H Mol. Wt Yield 561 75% Au 7. 71 (1H, d, J=15. 42 Hz)., 7. 56 (2H, d, J=8. 55 Hz), 7. 44 (1H, dd, J=17. 32Hz), 7. 26 (1H, dd, J=10. 41 Hz), 7. 10 (2H, d, J=8. 55 Hz), 6. 97 (1H, t, J=6. 62 Hz), 6. 88 (1H, d, J=15. 42 Hz), 4. 92 (lH, m), 4. 47 (2H, m), 4. 15 (1H, t, J=6. 1 Hz), 3. 82 (4H, m), 3. 75 (1H, m), 3. 10 (4H, m), 3. 07 (3H, s), 2. 32 (3H, s) (the solvent used was DMSO-d6) 92.) u'H H Mol. Wt Yield o 547 83% \-O 7. 58 (lH, d, J=18. 15 Hz), 7. 48 (1H, dd, J=14. 16 Hz), 7. 14 (lH, dd, J=12. 18 Hz), 7. 10 (1H, dd, J=9. 81 Hz), 7. 03 (1H, t, J=5. 91 Hz), 6. 97 (lH, d, 9. 11 Hz), 6. 83 (1H, d, J=18. 15 Hz), 6. 80 (1H, d, J=8. 1 Hz), 6. 01 (2H, s), 4. 92 (1H, m), 4. 47 (2H, m), 4. 20 (1H, t, J=6. 14 Hz), 3. 93 (1H, m), 3. 84 (4H, m), 3. 14 (3H, s), 3. 08 (4H, m). (solvent used is DMSO-d6) 93. H H Mol. Wt Yield 542 85% OWN H 10. 72 (1H, s), 8. 0 (lH, d, J=15. 30 Hz), 7. 50 (1H, dd, J=16. 74 Hz), 7. 44 (1H, m), 7. 42 (2H, m), 7. 26 (2H, m), 7. 10 (1H, dd, J=10. 21 Hz), 6. 98 (1H, t, J=6. 12 Hz), 6. 92 (1H, d, J=15. 30 Hz), 4. 92 (1H, m), 4. 43 (2H, m), 4. 13 (1H, t, J=5. 06 Hz), 3. 90 (lH, m), 3. 49 (lH, m), 3. 14 (3H, m), 3. 10 (4H, m). 94. H H Mol. Wt Yield 493 83% 0 7. 52 (1H, d, J=15. 06 Hz), 7. 49 (lH, dd, J=17. 37 Hz), 7. 45 (1H, d, J=3. 33 Hz), 7. 09 (1H, t, J=10. 41 Hz), 6. 96 (1H, t, J=6. 02 Hz), 6. 85 ( 1H, d, J=15. 06 Hz), 6. 56 (1H, d, 3. 33 Hz), 6. 45 (lH, m), 4. 92 (1H, m), 4. 45 (1H, m), 4. 15 (1H, t, J=6. 08 Hz), 3. 93 (lH, m), 3. 90 (4H, m), 3. 10 (4X m), 3. 08 (3H, s). 95. iry H H Mol. Wt Yield 504 100% 7. 59 (1H, d, J=15. 59 Hz), 8. 61 (2H, d, J=15. 76 Hz), 7. 70 (2H, d, J=6. 03 Hz), 7. 48 (1H, dd, J=15. 11 Hz), 7. 43 (1H, d, J=15. 59 Hz), 7. 09 (1H, t, J=6. 18 Hz), 5. 0 (lH, m), 4. 45 (2H, m), 4. 18 (1H, t, J=6. 22 Hz), 3. 82 (1H, m), 3. 73 (4H, m), 3. 24 (3H, s), 3. 0 (4H, m) (the solvent used was DMSO-d6) 96. H Mol. Wt Yield F) 521 94% 7. 67 (1H, d, J=15. 97 Hz), 7. 56 (2H, d, J=8. 7 Hz), 7. 47 (1H, dd, J=16. 65 Hz), 7. 13 (2H, d, J=8. 7 Hz), 7. 10 (lH, dd, J=10. 71 Hz), 7. 10 (1H, t, J=5. 69 Hz), 6. 85 (1H, d, J=15. 39 Hz), 4. 95 (1H, m), 4. 46 (2H, m), 4. 18 (1H, t, J=6. 12), 3. 94 (lH, m), 3. 89 (4H, m),. 87 (3H, s), 3. 09 (4H, m). (the solvent used was DMSO-d6) 97. H H Mol. Wt Yield 503 95% 7. 73 (1H, d, J=15. 42 Hz), 7. 52 (2H, m), 7. 45 (1H, dd, J=17. 3 Hz), 7. 38 (3H, m), 7. 26 (1H, dd, J=10. 8 Hz), 6. 97 (1H, t, J=6. 09 Hz), 6. 89 (1H, d, J=15. 42 Hz), 4. 91 (1H, m), 4. 45 (2H, m), 4. 12 (1H, t, J=6. 1 Hz), 3. 95 (1H, m), 3. 92 (4H, m), 3. 15 (3H, s), 3. 08 (Te m). 98. H H Mol. Wt Yield Meon 533 91% 7. 70 (1H, d, J=15. 33 Hz), 7. 50 (2H, d, J=8. 74 Hz), 7. 45 (lh, dd, J=17. 32 Hz), 7. 11 (1H, dd, J=10. 62 Hz), 6. 97 (1H, t, J=5. 14 Hz), 6. 94 (2H, d, J=8. 74 Hz), 6. 76 (1H, d, J=15. 36 Hz), 4. 91 (lH, m), 4. 45 (2H, m), 4. 15 (1H, t, J=6. 08 Hz), 3. 95 (1H, m), 3. 93 (3H, s), 3. 90 (4H, m), 3. 14 (3H, s), 3. 07 (4H, m).

Preparation 6

(S)-N-[3-(3-Fluoro-4-{4-[3-(thiophen-2-yl)-acryloyl]-piperaz inyl]-phenyl)-2-oxo- oxazolidin-5-yl-methyl azide. (Compound No. 99)

(S)-N- [3- (3-Fluoro-4- {4- [3- (thiophen-2-yl)-acryloyl]-piperazinyl]-phenyl)-2-oxo- oxazolidin-5-yl-methyl methane sulphonate (2g) was taken in dimethyl formamide (38ml) and sodium azide (0.97g) was added. The reaction mixture was heated to 70-75 °C over a period of 3 hrs. (TLC) and cooled to ca 30°C. The mixture was diluted with ethylacetate (500ml) and washed with DM water (200ml). The organic layer was separated and dried over anhydrous sodium sulphate. After evaporation of solvents, the residue obtained was triturated with petroleum ether to afford the title compound as an offwhite solid (1. 5g, 83%), mp 164-172 °C.

The following compounds were synthesized following the above procedure.

Table 6: 99. Z R4 R3 H H Mol. Wt. Yield 456 83% 7. 8 (1H, d, J=15. 06 Hz), 7. 4 (1H, dd, J=2. 4, 11. 7 Hz), 7. 3 (1H, d, J=5. 1 Hz), 7. 2 (1H, d, J=3. 3 Hz), 7. 0 (lH, dd, J=3. 6, 4. 9 Hz), 6. 9 (lH, t), 6. 6 (1H, d, J=15 Hz), 4. 7 (lH, m), 4. 0 (lH, t, J=9 Hz), 3. 7 (lH, m), 3. 1 (lH, m) (the solvent used was DMSO-d6 100. H H Mol. Wt Yield 508 80% 7. 71 (1H, d, J=15. 43 Hz), 7. 66 (2H, d, J=8. 52 Hz), 7. 50 (1H, dd, J=17. 31 Hz), 7. 10 (1H, d, J=8. 52 Hz), 6. 97 (1H, dd, J=10. 27 Hz), 6. 09 (1H,. t, J=6. 1 Hz), 6. 83 (1H, d, J=15. 42 Hz), 4. 92 (lH, m), 4. 08 (1H, t, J=5. 95 Hz), 3. 80 (4H, m), 3. 68 (lH, m), 3. 09 (4H, m), 2. 33 (3H, s) (the solvent used was DMSO-d6) 101. H Mol. Wt Yield 594 89% zozo 7. 65 (1H, d, J=15. 24Hz), 7. 50 (1H, dd, J=16. 5 Hz), 7. 14 (1H, dd, J=10. 11 Hz), 7. 10 (1H, dd, J=11. 16 Hz), 7. 03 (1H, t, J=6. 12 Hz), 6. 96 (1H, d, J=9. 15 Hz), 6. 79 (lH, d, J=8. 11 Hz), 6. 76 (1H, d, J=15. 24 Hz), 6. 0 (2H, s), 4. 78 (lH, m), 4. 08 (1H, t, J=5. 92 Hz), 3. 85 (2H, m), 3. 82 (4H, m), 3. 73 (lH, m), 3. 10 (4H, m) 102. H H Mol. Wt Yield 489 86% H H H, s), 7. 99 (1H, d, J=15. 3 Hz), 7. 58 (1H, dd, J=17. 31 Hz), 7. 48 (lH, m ), 7. 45 (2H, m), 7. 23 (2H, m), 7. 10 (lH, dd, J=17. 31 Hz), 7. 09 (1H, t, J=6. 0 Hz), 6. 90 (1H, J=15. 3 Hz), 4. 8 (lH, m), 4. 05 (1H, t, J=6. 11 Hz), 3. 92 (2H, m), 3. 89 (4H, m), 3. 72 (IFLm), 3. 1 (4H, m). 103. H H Mol. Wt Yield p 440 84% 7. 52 (lH, d, J=15. 43 Hz), 7. 49 (lH, dd, J=17. 34 Hz), 7. 45 (lH, d, J=3. 2 Hz), 7. 10 (1H, dd, J=10. 37 Hz), 6. 93 (lH, t, J=6. 03 Hz), 6. 80 (1H, d, J=15. 43 Hz), 6. 57 (1H, d, J=3. 3 Hz), 6. 45 (lH, m), 4. 92 (lH, m), 4. 08 (1H, t, J=5. 94 Hz), 3. 90 (2H, m), 3. 90 (4H, m), 3. 73 (lH, m), 3. 09 (4H, m) 104. 1 H H Mol. Wt Yield NovJ 451 84% 8. 61 (2H, d, J=5. 88 Hz), 7. 70 (2H, d, J=5. 99 Hz), 7. 59 (1H, d, J=15. 66 Hz), 7. 54 (lH, dd, J=1, 4. 8 Hz), 7. 43 (1H, d, J=15. 6 Hz), 7. 22 (1H, dd, J=11. 0 Hz), 7. 09 (1H, t, J=6. 17 Hz), 4. 89 (lH, m), 4. 07 (1H, t, J=6. 10 Hz), 3. 77 (2H, m), 3. 72 (4H, m), 3. 65 (lH, m), 3. 0 (4H, m) (the solvent used was DMSO-d6) 1- 105. H H Mol. Wt Yi 1-d- 468 70% r 7. 69 (lH, d, J=15. 42 Hz), 7. 54 (2H, d, J=8. 7 Hz), 7. 44 (lH, dd, J=16. 68 Hz), 7. 11 (2H, d, J=8. 7 Hz), 7. 07 (1H, dd, J=10. 11 Hz), 6. 93 (1H, t, J=6. 11 Hz), 6. 80 (1H, d, J=15. 42 Hz), 4. 78 (lH, m), 4. 08 (1H, t, J=5. 93 Hz), 3. 90 (2H, m), 3. 80 (4H, m), 3. 60 (lH, m), 3. 09 (4H, m). 106 < | | H | Mol. Wt | Yield 106. H H Mol. Wt Yield 462 85% 7. 73 (2H, m), 7. 59 (lH, dd, J=15. 14Hz), 7. 38 (3H, m), 7. 22 (lH, d, J=15. 14Hz) 7. 18 (lH, dd, J=9. 78Hz), 7. 09 (lH, t, J=6. 01Hz), 4. 88 (lH, m), 4. 10 (lH, t, J=6. 10 Hz), 3. 86 (4H, m), 3. 73 (2H, m), 3. 65 (lH, m), 2. 99 (4H, m) (the solvent used was DMSO-d6) 107. H H Mol. Wt Yield- Mep I 492 84% MeO' 7. 65 (IH, d, J=15. 3Hz), 7. 50 (2H, d, J=8. 64Hz),. 44 (lH, dd, J=16. 2Hz), 7. 04 (IH, dd, J=9. 14Hz), 6. 94 (2H, d, J=-8. 64Hz), 6. 91 (lH, t, J=6. 02Hz) 6. 80 (lH, d, J=15. 2Hz), 4. 9 (lH, m), 4. 32 (lH, t, J=6. 1), 3. 98 (4H, m), 3. 92 (2H, m), 3. 89 (lH, m), 3. 07 (4H, m) (the solvent used was DMSO-d6)

Preparation 7:

(S)-N- [3- (3-Fluoro-4- 4- [3- (thiophen-2-yl)-acryloyl]-piperazinyl}-phenyl)-2-oxo- oxazolidin-5-yl-methyl amine (compound No. 108) (S)-N- [3- (3-Fluoro-4- {4- [3- (thiophen-2-yl)-acryloyl]-piperazinyl]-phenyl)-2-oxo- oxazolidin-5-yl-methyl azide (1.25g) and triphenylphosphine (0.860g) were taken in a mixture of 1, 4-dioxane: methanol (25mL : 5mL) at ca 27 °C and stirred for 1 hour. To this was added aqueous ammonia (8mL) at ca 27 °C and stirred for another 1 hour (TLC).

The solvents were removed under reduced pressure to afford crude oil, which was triturated with diisopropyl ether to afford title compound (lg, 85%), m. p. 195-200 °C The following compounds were made following above procedure.

Table 7: 108. Z R4 R3 H H Mol. Wt. Yield 430 85% 7. 8 (1H, d, J=15. 06 Hz), 7. 5 (IH, dd, J=2. 7, 11.. 7 Hz), 7. 3 (1H, d, J=5. 1 Hz), 7. 2 (lH, d, J=3. 3 Hz), 7. 1 (lH, dd, J=2. 4 Hz), 7. 03 (1H, t, J=4. 8, 3. 6 Hz), 6. 6 (lH, d, J=15. 06 Hz), 4. 6 (lH, m), 4. 0 (lH, t, J=8. 7 Hz), 3. 8 (4H, m), 3. 0 (4H, m) (the solvent used is DMSO-d6) 109./H H Mol. Wt Yield Ho 440 69% 9. 67 (lH, br), 7. 67 (lH, d, J=15. 42 Hz), 7. 53 (2H, d, J=7. 88 Hz), 7. 45 (1H, dd, J=17. 32 Hz), 7. 17 (1H, dd, J=10. 32 Hz), 7. 11 (1H, d, J=15. 42 Hz), 7. 08 (1H, t, J=4. 99 Hz), 6. 78 (2H, d, J=7. 88 Hz), 4. 73 (1H, m), 4. 11 (1H, t, J=5. 38 Hz), 3. 97 (2H, m), 3. 82 (1H, m), 3. 80 (4H, m), 3. 10 (4H, m). (solvent used is DMSO-d6) 110. l | H | Mol. Wt Yield 468 80% zozo 7. 65 (1H, d, J=15. 27 Hz), 7. 46 (1H, dd, J=16. 8 Hz), 7. 12 (1H, d, J=10. 12 Hz), 7. 0 (1H, dd, J=15. 27 Hz), 6. 96 (1H, t, J=6. 21 Hz), 6. 92 (1H, d, J=9. 15 Hz), 6. 79 (1H, d, J=7. 95 Hz.), 6. 71 (1H, d, J=15. 27 Hz), 6. 0 (2H, s), 4. 91 (1H, m), 4. 04 (1H, t, J=5. 8 Hz), 3. 89 (2H, m), 3. 85 (1H, m), 3. 80 (4H, m), 3. 09 (4H, m). (the solvent used is DMSO-d6) Ill. H H Mol. Wt Yield 463 80% CON H 11. 65 (1H, s), 7. 96 (1H, d, J=15. 3 Hz), 7. 76 (1H, dd, J=17. 32 Hz), 7. 45 (1H, m), 7. 42 (2H, m), 7. 21 (2H, m), 7. 13 (1H, dd, J=10. 62 Hz), 7. 09 (lH, t, J=5. 88 Hz), 6. 96 (1H, d, J=15. 3 Hz), 4. 82 (1H, m), 4. 05 (1H, t, J=6. 02 Hz), 3. 84 (4H, m), 3. 82 (4H, m), 3. 79 (lH, m), 3. 0 (4H, m). (the solvent used is DMSO-d6 112. H H Yield o t l 386 82% 7. 54 (1H, dd, J=17. 37 Hz), 7. 49 (lH, d, J=2. 38 Hz), 7. 38 (1H, d, J=15. 17Hz), 7. 18 (1H, dd, J=10. 18 Hz), 7. 06 (1H, t, J=6. 12 Hz), 6. 92 (lH, d, J=15. 17 Hz), 686 (1H, d, J=2. 38 Hz), 6. 60 (lH, m), 4. 58 (lH, m), 4. 04 (lH, t, J=4. 58 Hz), 3. 803 (4H, m), 3. 78 (2H, m), 3. 146 (lH, m), 2. 97 (4H, m), 3. 10 (4H, m). (the solvent used is DMSO-d6) l 113, 1 H H Mol. Wt Yield my 8. 61 (2H, d, J=8. 88 Hz), 7. 70 (2H, d, J=6 Hz), 7. 5 (1H, d, J=15. 36 Hz), 7. 54 (1H, dd, J=16. 38 Hz), 7. 48 (lH, dd, J=16. 38 Hz), 7. 48 (1H, d, J=15. 38 Hz), 7. 19 (lH, dd, J=10. 11 Hz), 4. 59 (1H, m), 4. 05 (1H, m), 4. 05 (1H, t, J=5. 93 Hz), 3. 86 (2H, m), 3. 81 (4H, m), 3. 72 (1H, m), 2. 98 (4H, m). (the solvent used is DMSO-d6) 114. H H Mol. Wt Yield 442 92% F 7. 70 (1H, d, J=15. 39 Hz), 7. 54 (2H, d, J=8. 43 Hz), 7. 47 (1H, dd, J=16. 11 Hz), 7. 12 (2H, d, J=8. 43 Hz), 7. 07 (1H, dd, J=9. 78 Hz), 6. 93 (1H, t, J=6. 13 Hz), 6. 81 (1H, d, J=15. 39 Hz), 4. 66 (lH, m), 4. 04 (1H, t, J=5. 8 Hz), 3. 98 (2H, m), 3. 83 (4H, m), 3. 80 (lH, m), 3. 10 (4H, m) 115. w H H Mol. Wt Yield 436 76% 7. 73 (2go), 7 54 (1H, d, J=15. 31 Hz), 7. 42 (lH, dd, J=16. 37 Hz), 7. 38 (3H, m), 7. 29 (1H, d, J=15. 31 Hz), 7. 18 (1H, dd, J=10. 86 Hz), 7. 05 (lH, t, J=6. 15 Hz), 4. 64 (lH, m), 4. 08 (1H, t, J=5. 97 Hz), 3. 85 (4H, m), 3. 81 (2H, m), 3. 72 (lH, m), 2. 98 (4H, m) (the solvent used is DMSO-de) is DMSO-d6) 116. H H Mol. Wt Yield J) J 464 75% Mu0 7. 676 (1H, d, J=15. 4 Hz), 7. 52 (2H, d, J=8. 52 Hz), 7. 41 (1H, dd, J=17. 2 Hz), 7. 08 (1H, dd, J=10. 14 Hz), 7. 1 (2H, d, J=8. 52 Hz), 6. 98 (lH, t, J=6. 1Hz), 6. 78 (lH, d, J=15. 4 Hz), 4. 9 (lH, m), 4. 25 (1H, t, J=6. 2 Hz), 4. 11 (4H, m), 3. 99 (2H, m), 3. 90 (lH, m) 3. 09 (4H, m) Preparation No. 8

(S)-N- [3- (3-Fluoro-4- {4- [3- (thophen-2-yl)-acryloyl]-piperazinyl]-phenyl)-2-oxo- oxazolidin-5-yl-methyl thioisocynate (compound No. 117) A mixture of (S)-N- [3- (3-Fluoro-4- {4- [3- (thiophen-2yl)-acryloyl]-piperazinyl]-phenyl)- 2-oxo-oxazolidin-5-yl methyl amine (1g) CS2 (0.13 ml) and Et3N (. 5 ml) in THF (10 ml) was stirred at ca 30 °C for 5 hours. Then ethyl chloroformate (0.30 ml) was added to the mixture and stirred at the same temp for 1 hour (TLC). The mixture was qunched with DM water (25 ml) and extracted with EtOAc (100 ml). The extract was washed with brine (25 ml), again separated the organic layer, dried and concentrated under vacuum initially afforded an oil, which was triturated with diisopropyl ether to give title compound (lg, 91%).

The following compounds were made following above procedure Table 8: 117. Ra rus Mol. Wt. Yield H H 472 91% 7. 8 (1H, d, J=15. 06Hz) 7 7. 4 (1H, dd, J=2. 4Hz), 7. 3 (1H, d, J=5. 1 Hz), 7. 2 (1H, t, J=8. 1, 3. 3 Hz), 7. 0 (1H, dd, J=3. 9, 1. 2 Hz), 6. 9 (1H, t, J=9. 3 Hz), 6. 6 (1H, d, J=15. 06 Hz), 4. 8 (1H, m), 4. 1 (1H, t, J=9 Hz), 3. 8 (4H, m), 3 09 (4H, m). (solvent used is DMSO-d6 118. H H Mol. Wt Yield 450 86% W0 I l 7. 4 (lH, dd, J=6. 12 Hz), 7. 0 (2H, d, J=8. 7 Hz), 6. 9 (lH, m), 6. 0 (lH, t), 4. 7 (lH, m), 4. 0 (lH, t), 2. 02 (3H, s), 3. 0 (8H, complex) 3 7 (3H, m) 119. r H H Mol. Wt Yield F/484 32% F 7 8 (2H, d, J=8. 59 Hz), 7. 53 (1H, d, J=15 Hz), 7. 48 (1H, dd, J=16. 31 Hz) 7. 23 (2H, d), 7. 13 (1H, dd, J=10 Hz), 7. 06 (1H, t) 4. 96. (1H, m), 4. 08 (1H, t), 3. 85 (4H, m), 3. 75 (1H, m), 3. 44 (2H, m), 3. 09 (4H, m) (solvent used is DMSO-d6) Preparation No. 9

(S)-N- [3- (3-Fluoro-4- {4- {3- (thiophen-2-yl)-acryloyl]-piperzinyl)-phenyl)-2-oxo- oxazoldin-5-yl-methyl thiocarbamate (compound No. 120).

To solution of NaH (60% in oil, O. lOg) in methanol (10 ml), a mixture of compound No. 117 (1 g) in methanol (10 ml) was added under ice cooling followed by stirring of ca 27 °C for 3 h (TLC). The reaction mixture was poured into ice water and adjusted pH 7 with dilute HCl. The solid collected was purified through column chromatography using

eluant 0-4 % methanol in CHCl3. The solution was concentrated to afford the title compound (300 mg, 29%) mp 180-185 °C.

The following compounds were made following above procedure.

Table 9: 120. Z R4 R3 Mol. Wt. Yield H 504 78% ' 7. 8 (1H, d, J=15. 06 Hz), 7. 4 (1H, d, J=11. 7 & 2. 7 Hz), 7. 3 (1H, d, J=5. 1 Hz), 7. 2 (1H, t, J=6. 6 &3. 3 Hz), 6. 6 (1H, d, J=15. 06 Hz), 4. 9 (1H, m), 4. 0 (4H, m), 3. 8 (4H, m) (the solvent used was DMSo-d6) 121. X H H Mol. Wt Yield 493 83% 8. 7 (lH, d, J=1. 71 Hz), 8. 5 (1H, d, J=3. 86 Hz), 8. 1 (1H, d, J=8. 04 Hz), 7. 6 (2H, d, J=15. 57 Hz), 7. 2 (1H, d, 5=15, 57 Hz), 7. 0 (1H, t, J=9. 12 Hz), 4. 8 (1H, t, J=9 Hz), 3. 5 (2H, d, J=4. 95 Hz), 1. 95 (3H, s), 7. 5 (2H, m), 7. 1 (1H, dd, J=1. 86 Hz), 4. 0 (1H, t, J=9. 0 Hz), 3. 9 (4H, t), 3. 7 (1H, m), 3. 1 (4H, t), 4. 7 (1H, m) 122. m H H Mol. Wt Yield 450 86% -o 7. 4 (1H, dd, J=6. 12 Hz), 7. 0 (2H, d, J=8. 7 Hz), 6. 9 (lH, m), 6. 0 (1H, t), 4. 7 (1H, m), 4. 0 (lH, t), 2. 02 (3H, s), 3. 0 (8H, complex) 3. 7 (3H, m) (the solvent used is DMSO-d6) Preparation 10

(3/-N- [3- (3-Fluoro-4- {4- (thiophen-2-yl)-acryloyl]-piperazineyl]-phenyl)-2-oxo- oxazolidin-5-yl-methyl] thiourea (compound No. 123) A mixture of (S)-N- [3- (3-Fluoro-4- {4- [3- (thiophen-2-yl)-acryloyl]-piperazinyl]-phenyl)- 2-oxo-oxazolidin-5-yl-methylamine (0. 5g) CS2 (0.09 ml) and Et3N (0.25 ml) in THF. (5 ml) was stirred at ca 30 °C for 5 hours. Then ethylchloroformate (0.15 ml) was added to the mixture and stirred at ca 30 °C for 1 hour (TLC). The mixture was quenched with DM water (10 ml) and extracted with EtOAc (50 ml). The extract was dried over anhy. Na2S04 and concentrated under vacuum to afford oil (0.5 g) which was taken in methanol (10 ml) and to this stirred solution added a solution of 16% ammonia gas in methanol (10 ml) for 1 hour at Ca 27 °C (TLC) solid began to separate, which was filtered to afford the title compound as white solid (0.25g, 60%) mp 154-157 °C The following compounds prepared following the above procedure.

Table 10: 123. Z R4 R3 Mol. Wt. Yield H H 489 60% '\S 7. 83 (1H, d, J=15. 06 Hz), 7. 72 (1H, br), 7. 39 (IH, d, J=5. 04 Hz), 7. 34 (1H, dd, J=17. 32 Hz), 7. 22 (lH, d, J=3. 4 Hz), 7. 07 (lH, m), 7. 04 (1H, dd, J=8. 7 Hz), 6. 92 (1H, t, J=6. 1 Hz), 6. 72 (1H, d, J=15. 06 Hz), 6. 32 (2H, br), 4. 91 (1H, m), 4. 36 (IH, t, J=5. 98 Hz), 4. 11 (2H, m), 4. 04 (1H, m), 3. 91 (4H, m), 3. 06 (4H, m). (the solvent used is DMSO-d6) 124. H H Mol. Wt Yield HO) 499 40% 7. 90 (1H, d, J=15. 2 Hz), 7. 56 (2H, d, J=8. 44 Hz), 7. 45 (1H, dd, J=15. 5 Hz), 7. 19 (1H, dd, J=8. 70 Hz), 7. 10 (1H, t, J=6. 17 Hz), 7. 03 (1H, d, J=15. 2 Hz), 6. 78 (2H, d, J=8. 44 Hz), 4. 53 (lH, m), 4. 08 (1H, t, J=5. 78 Hz), 4. 0 (2H, m), 3. 98 (1H, m), 3. 80 (4H, m), 3. 31 (4H, m). (the solvent used is DMSO-d6) 125. H H Mol. Wt Yield 527 45% zozo 7. 61 (1H, d, J=15. 31 Hz), 7. 38 (1H, dd, J=15. 9 Hz), 7. 07 (1H, d, J=9. 16 Hz), 7. 02 (1H, dd, J=8. 16 Hz), 6. 99 (1H, s), 6. 91 (1H, dd, J=10. 2 Hz), 6. 85 (1H, t, J=6. 0 Hz), 6. 76 (1H, d, J=15. 3 Hz), 6. 71 (2H, br), 5. 99 (2H, s), 4. 90 (lH, m), 4. 15 (1H, t, J=6. 11 Hz), 3. 89 (lH, m), 3. 84 (4H, m), 3. 05 (4H m). 126/H H Mol. Wt Yield 522 53% OWN H 10. 38 (1H, s), 7. 94 (1H, d, J=15. 27 Hz), 7. 51 (1H, dd, J=17. 32 Hz), 7. 47 (2H, m), 7. 44 (lH, s), 7. 35 (2H, m), 7. 22 (1H, dd, J=10. 5 Hz), 7. 07 (1H, t, J=6. 05 Hz), 6. 94 (1H, d, J=15. 51 Hz), 6. 89 (2H, br), 4. 87 (lH, m), 4. 15 (1H, t, J=4. 76 Hz), 4. 08 (2H, m), 4. 01 (lH, m), 3. 92 (4H, m), 3. 10 (4H, m) (solvent used is CDC13+ DMSO-d6). 127./r\ H H Mol. Wt Yield NO./I, 473 40% 0 7. 72 (lH, br), 7. 48 (1H, d, J=15. 02 Hz), 7. 45 (lH, m), 7. 39 (1H, dd, J=16. 38 Hz), 7. 04 (1H, dd, J=10. 81 Hz), 6. 89 (1H, t, J=6. 1 Hz), 6. 79 (1H, d, J=15. 01 Hz), 6. 58 (1H, d, J=3. 3 Hz), 6. 47 (1H, d, J=3. 24 Hz), 6. 32 (2H, br), 4. 91 (1H, m), 4. 08 (1H, t, J=5. 9 Hz), 4. 02 (1H, m), 3. 91 (2H, m), 3. 79 (4H, m), 3. 05 (4H, m). 128. N/\ H 0 my 8. 61 (2H, d, J=5. 93 Hz), 7. 70 (2H, d, J=6. 01 Hz), 7. 59 (1H, d, J=15. 35 Hz), 7. 54 (IH, dd, J=16. 28 Hz), 7. 48 (1H, d, J=15. 35 Hz), 7. 20 (1H, dd, J=10. 95 Hz), 7. 05 (1H, t, J=6. 16 Hz), 4. 81 (IH, m), 4. l l (lH, t, J=5. 97 Hz), 3. 87 (2H, m), 3. 79 (4H, m), 3. 50 (1H, m), 2. 99 (4H, m). (solvent used is CDC13+ DMSO-d6). H H Mol. Wt Yield ,. SOI 79% F 7. 80 (2H, d, J=9. 0 Hz), 7. 53 (1H, dd, J=17. 31 Hz), 7. 23 (1H, dd, J=10. 81 Hz), 7. 22 (1H, t, J=6. 09 Hz), 7. 11 (1H, d, J=9 Hz), 7. 08 (1H, d, J=15. 22 Hz), 4. 81 (lH, m), 4. 0 (1g t, J=5. 98 Hz), 3. 84 (4H, m), 3. 79 (lH, m), 3. 73 (4H, m), 2. 98 (4H, m). (solvent used is DMSO- d6) 130. H H Mol. Wt Yield 483 67% 7. 68-7. 70 (1H, d, J=15. 42 Hz), 7. 52-7. 55 (1H, dd, J=17. 4 Hz), 7. 3 (5H, m), 7. 0 (1H, dd, J=10. 56 Hz), 6. 9 (1H, d, J=15. 33 Hz), 6. 89 (1H, t, J=7. 66 Hz), 6. 27 (2H, br), 4. 9 (lH, m), 4. 60 (1H, t, J=5. 9 Hz), 4. 15 (2H, m), 4. 10 (2H, m), 4. 06 (4H, m), 2. 99 (4H, m). l 131. H H Mol. Wt Yield MeO" 513 70% MeO" 7. 6 (1H, d, J=15. 27 Hz), 7. 5 ( in, d, J=8. 52 Hz), 7. 3 (1H, dd, J=16. 08 Hz), 7. 0 (lH, dd, J=7. 14 Hz), 6. 9 (2H, d, J=8. 52 Hz), 6. 91 (1H, t, J=5. 21 Hz), 6. 7 (1H, d, J=15. 3 Hz), 6. 2 (2H, br), 4. 9 (1H, m), 4. 35 (1H, t, J=5. 91 Hz), 4. 11 (2H, m), 3. 98 (1H, m), 3. 9 (4H, m), 3. 92 (3H, s), 3. 08 (4H, m) Preparation 11

N- (3- {3-fluoro-4- [4- (3-phenyl-allyl)-piperazin-1-yl] phenyl}-2-oxo-oxazolidin-5-yl- methyl) acetamide. (compound No. 132) A mixture of 3- (3-Fluoro-4-piperazinyl-phenyl)-2-oxo-5-oxazolidinyl) acetamide (0.5 g), 10 mL acetone and potassium carbonate (0.205 g) was stirred at ca 27 °C for 1 hour. The Cinnamoyl chloride (0. 226 g) was added to this mixture at ca 27 °C and left the reaction mixture overnight (TLC). The mixture was quenched with DM water (25 mL) and extracted with 50 mL of chloroform. The organic layer was separated and dried over anhydrous Na2S04 and concentrated under vacuum to afford an oil. The crude product was purified through column chromatography by using eluent as 0-3. 5 % MeOH in CHCl3. The distillation of solvents afforded the title compound as white solid (0.15 g, 22 %), m. p 134-136 ° C. 132. w H H Mol. Wt Yield 452 44 % 7. 45 (5H, m), 7. 3 (2H, t, J=6. 99) 7. 0 (lH, dd, J=2. 2, 8. 7), 6. 9 (lH, t, =9), 6. 5 (lH, d, J=15. 84), 6. 0 (lH, t), 4. 7 (lH, m), 4. 0 (lH, t, J=9), 3. 7 (3H, m), 3. 2 (2H, d), 3. 1 (4H, s), 2. 2 (4H, s), 2. 0 (3H, s).

The compounds of the present invention have useful activity against a variety of organisms. The invitro activity of compounds of the present invention can be assessed by standard testing procedures such as the determination of minimum inhibitory concentration (MIC) by standard"Microdilution method"as described elsewhere in the specification. The pharmacokinetic profiling of the compounds were also done according to the protocol described in this specification. The activities of representative compounds of the present invention are given below in the following table.

Guide to table abbreviations: MRSA : Methicillin resistant Staphylococus aureus 6538P SE Staphylococcus epidermidis ATCC 12228 EF Enterococcus faecalis ATCC 29212 SA Staphylococus aureus ATCC 33591 Table: MIC (µg/ml) in vitro activity in gram positive organisms. Sl. Compound No. SA SE EF SA No. 1 01 0. 5 2. 05 1 0.5 0.5 2 3. 64 0. 5 0. 25 0. 25 0. 25 4. 66 1 0. 5 0. 5 0. 5 5. 70 1 2 0, 5 0. 5 6 123 0. 5 0. 25 1 7. 124 1 0. 5 1 1 8. 125 1 2 0. 5 4 9. 126 1 0.5 1 1 10. 127 2 0. 5 1 2 11 Linezolid 2 4 4 4 12. Eperzolid 2 4 2 4