4-thia-1-aza-bicyclo�4,2,0!oct-2-ene antibiotics

STATE OF THE ART
In European Patent application No. 0153229, there are described new derivatives of 1-dethia 2-thia cephalosporanic acids and their salts, their preparation process and their use as medicaments. The said products have the formula. ##STR5## wherein R is either ##STR6## in which Ra is an organic radical, or ##STR7## in which Ri and Rj individually are hydrogen or an aliphatic or aromatic hydrocarbon or a heterocyclic or Ri and Rj form with the nitrogen atom to which they are bonded an optionally substituted or Rb-- in which Rb is an optionally substituted carbocyclic or heterocyclic aryl, R.sub.1 is a) --Z--R.sub.2 in which R.sub.2 is an alkyl, alkenyl or alkynyl optionally substituted or interrupted by a heteroatom and Z is an optionally oxidized sulfur, selenium, oxygen or --NH--, b) --Z.sub.a --R.sub.3 in which R.sub.3 is an optionally substituted carbocyclic or heterocyclic aryl or an optionally substituted quaternary ammonium and Z.sub.a is methylene, sulfur, selenium or oxygen or --NH-- or Z.sub.a is a simple bond or Z.sub.a is --CH.sub.2 --S--, c) and alkyl, alkenyl or alkynyl of 2 to 8 carbon atoms optionally substituted or interrupted by a heteroatom, d) halogen, nitrile, optionally esterified or salified carboxy, azido, thiocyanato or isothiocyanato or e) azinomethyl, amino or mono- or di-substituted methyl amino, thiocyanatomethyl, isothiocyanato methyl, carbamoyloxy-methyl, semicarbazonomethine, optionally substituted arylhydrazonomethine, nitromethyl or di or tri-halomethyl --CH.sub.2 --ONO.sub.2, CH.sub.2 --.sup..sym. p(alk).sub.3 or ##STR8## alk is alkyl of 1 to 4 carbon atoms, R.sub.4 is hydrogen or methoxy, COM is --CO.sub.2 --A in which A is hydrogen, an alkali metal, alkaline earth metal, magnesium, ammonium or an organic amine or A is an ester group, or --CO.sub.2 A is CO.sub.2.sup.-, or R.sub.1 and CO.sub.2 A form together with the carbon atoms to which they are bonded. ##STR9## or COM is an optionally substituted carbamoyl and n.sub.2 is an integer equal to 0, 1 or 2, as well as the non-toxic, pharmaceutically acceptable addition salts. The products of the above formula can be in racemic or optically-active form.
OBJECTS OF THE INVENTION
It is an object of the invention to provide the novel compounds of formula I and their non-toxic, pharmaceutically acceptable acid addition salts and a novel process for their preparation.
It is another object of the invention to provide novel anti-bacterial compositions and a novel method of combatting bacterial infections in warm-blooded animals.
These and other objects and advantages of the invention will become obvious from the following detailed description.
THE INVENTION
The novel compounds of the invention are selected from the group consisting of a compound of the formula ##STR10## wherein R is selected from the group consisting of ##STR11## and R.sub.b --NH--, Ra is an organic radical, Ri and Rj are individually selected from the group consisting of hydrogen, aliphatic hydrocarbon, aromatic hydrocarbon and heterocycle or taken together with the nitrogen atom to which they are attached form an optionally substituted ring, Rb is selected from the group consisting of carbocyclic aryl and heterocyclic aryl, both optionally substituted, R.sub.1A is selected from the group consisting of ##STR12## and ##STR13## are individually selected from the group consisting of hydrogen and alkyl of 1 to 4 carbon atoms, Z.sub.A is selected from the group consisting of a simple bond, --O-- and optionally oxidized sulfur, R.sub.3A is selected from the group consisting of optionally substituted carbocyclic aryl and heterocyclic aryl, optionally substituted quaternary ammonium, acetyl carbamoyl, aldoxycarbonyl, alkyl and haloalkyl of 1 to 4 carbon atoms, --CN and azido, R.sub.4 is selected from the group consisting of hydrogen and methoxy, A is selected from the group consisting of hydrogen, alkali metal, alkaline earth metal, magnesium, --NH.sub.4, an organic amine and esterified carboxy or --COOA is --COO.crclbar., n.sub.2 is an integer from 0 to 2 and their non-toxic, pharmaceutical acceptable acid addition salts.
Among the products of formula I, wherein Z.sub.A is sulfur or oxygen and R.sub.3 A is a quaternary ammonium, the products are preferred in which Z.sub.A is not connected directly to the nitrogen atom. The products of formula I can be in the racemic or the optically active form.
Among the preferred values for R, R is acylamino of the formula ##STR14## wherein Ra is an organic radical.
Among the values for Ra are ##STR15## wherein Ar is phenyl optionally mono- or polysubstituted or an aromatic heterocyclic with 5, 6 or 7 ring atoms having 1 to 4 hetero-atoms chosen from sulfur, oxygen and nitrogen, n is an integer from 0 to 4, R.sub.5 is selected from the group consisting of amino, hydroxyl, azido, hydrazino, free, esterified or salified carboxyl, free or salified sulfo, sulfoamino, halogen, alkyl hydrazino, phenyl hydrazino and formyloxy.
Among the substituents for phenyl or heterocyclic are halogen and alkyl and alkoxy of 1 to 4 carbon atoms, amino alkyl of 1 to 4 carbon atoms, and preferably aminomethyl, hydroxyl, nitro, amino, trifluoromethyl or cyano. Among the heterocyclic aromatic, there are thiazolyl, furyl, thienyl, pyrrolyl, pyridinyl, pyrazinyl, pyrimidinyl, morpholinyl and tetrazolyl. Furyl, aminothiazolyl, aminohalo thiazolyl, amino thiadiazolyl and amino pyrimidinyl are preferred.
2) Ra may also be alkyl, cycloalkyl, alkoxyl, alkenyl or cycloalkenyl each of which may be mono- or poly-substituted by at least one substituent such as alkylthio or cyanoalkylthio, mercapto, nitro, cyano, or amino.
3) Ra may also be: ##STR16## wherein Rc has the same definition as Ar. Among the preferred values for Rc are: 2-amino-4-thiazolyl; 2- amino-5-nitro, 5-chloro, 5-fluoro or 5-bromo thiazolyl; 5-amino-1,2,4-thiadiazolyl, 4-thiazolyl, 2-thienyl or 2-furyl; Rd is hydrogen, acyl, aryl, heteroaryl, arylalkyl, heteroarylalkyl, alkyl, cycloalkyl, alkenyl or cycloalkenyl, alkynyl optionally substituted and optionally interrupted by oxygen or sulfur optionally oxidized or Rd may be optionally substituted carbamoyl.
Among the substituents of Rd are alkyl, halogen, acyl, cyano, carbamoyl, nitro, amino, hydroxy, mercapto, alkylthio, oxo, alkoxy or a free, esterified or salified carboxyl.
Among the values for Rd are hydrogen, alkyl, alkenyl, optionally cyclic, alkynyl, aryl, heteroaryl mono or polycyclic and particularly the values: ##STR17##
Among the preferred values for Rd are methyl, hydrogen, ethyl, allyl, 1-methyl-1-carboxyethyl, carboxymethyl and difluoromethyl.
4) Ra may also be: ##STR18## wherein Re has the same values as Ar. The non-substituted phenyl is preferred. Rf is alkyl optionally substituted, or --N.dbd.CH--Rg in which Rg is aryl as defined above for Ra. Ethyl, phenyl or furyl are preferred for Rf.
5) Ra may also be: ##STR19## wherein Rh has the values indicated for Ar and Rk is: ##STR20## in which R1 is hydrogen, alkylsulfonyl or --N.dbd.CH--Rm where Rm has the same value as Ar, in particular furyl; Rk may be an optionally substituted aryl, for example, imidazolyl substituted by a carboxyl. Rk may also be a substituted amino, for example, an acylamido such as N-methyl-benzoylamido or furylcarbonyl or an amino substituted by an optionally substituted heterocycle or Rk may be aryl optionally substituted and condensed; or optionally substituted aralkyl.
In this preferred class of products, Ra may preferably be: ##STR21##
Among other values for R, a second preferred class of products is constituted, preferably, by products in which R is: ##STR22## wherein Ri and Rj are individually selected from the group consisting of hydrogen or alkyl of 1 to 8 carbon atoms, or Ri and Rj form with the nitrogen atom to which they are connected a possibly substituted cyclic amine.
Preferably, ##STR23## is: ##STR24##
Among other values for R, a third preferred class of products is constituted preferably, by the products in which R is Rb--NH-- in which Rb is a carbocyclic or heterocyclic aryl optionally substituted
Among those preferred values are: ##STR25## in which Rp is alkyl of 1 to 4 carbon atoms, preferably methyl, ethyl, isopropyl optionally interrupted by a hetero-atom such as methoxymethyl, optionally substituted by one or more halogens such as trichlorethoxymethyl or trifluoroethoxymethyl or alkoxy such as ethoxy. Rp may also be arylalkyl such as benzyl or phenethyl optionally substituted by an alkyl such as methyl, alkoxy such as methoxy, cyano or halogen such as fluoro. Rp may also be furfuryl, or optionally substituted phenyl methoxymethyl.
Rq may be hydrogen or alkyl of 1 to 4 carbon atoms such as methyl, an alkoxycarbonyl such as methoxycarbonyl or tert-butyloxycarbonyl.
Among the preferred values for R, ##STR26## is preferred.
Among the values for R.sub.3A there can be cited the following: phenyl, diphenyl, naphthyl, thienyl, furyl, pyrrolyl, imidazolyl, pyrazolyl, thiazolyl, isothiazolyl, oxazolyl, isoxazolyl, triazolyl, thiadiazolyl, oxadiazolyl, tetrazolyl, pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, thiazinyl, oxazinyl, triazinyl, thiadiazinyl, oxadiazinyl, tetrazinyl, imidazolinyl, benzimidazolyl, benzothiazolyl, benzoxazole.
Among the different aryls, the following are preferred: thiazol-2-yl, 1,2,4-thiadiazol-5-yl and 1,2,4-thiadiazol-5-yl, imidazol-2-yl, 1,3,4-triazol-5-yl, 1,3,4-thiadiazol-2-yl, 1,2,3-thiadiazol-5-yl, lH-tetrazol-5-yl, pyridin-2yl, 1,3,4-triazin-2-yl, 1,3,5-triazin-4-yl, pyridinium, quinolinium, isoquinolinium, cyclopentylpyridinium, trimethylammonium.
R.sub.3A can be substituted by at least one radical chosen from alkyls such as methyl, ethyl, propyl, isopropyl, linear or branched butyl which alkyls can themselves be substituted by an aryl such as phenyl or thienyl, aryloxy such as lower phenoxy, alkoxy such as methoxy, alkoxy carbonyl such as ethoxycarbonyl, by a halogen such as chloro- or bromo, hydroxy free or protected, free carboxy, esterified or salified, amino, alkylamino or dialkylamino or acylamido.
R.sub.3A can also be substituted by at least one alkenyl such as vinyl, allyl, butenyl, alkynyl such as ethynyl or propargyl, aryl such as phenyl, tolyl, halogen such as chloro, bromo, iodo or fluoro, amino or nitro, alkoxy of 1 to 4 carbon atoms such as methoxy, alkylthio such as methylthio, hydroxy, mercapto, amino, free, esterified or salified carboxyl or carbamoyl. R.sub.3A can also be substituted by two substituents forming together a cycle such as cyclopentyl or cyclohexyl.
A particularly preferred catergory is constituted by the substituents R.sub.3A including a quaternary ammonium, in particular the substituents: ##STR27## the symbol representing the remainder of a ring. R.sub.3 A may also preferably be a non-cyclic quaternary ammonium.
Among the values for R.sub.1A, the following are preferred: ##STR28##
Among the values for A are sodium, potassium, lithium, calcium, magnesium, ammonium or of an organic base such as methylamine, propylamine, trimethylamine, diethylamine, triethylamine, N,N-dimethyl-ethanolamine, tris(hydroxymethyl) amino methane, ethanolamine, pyridine, picoline, dicyclohexylamine, morpholine, benzylamine, procaine, lysine, arginine, histidine, and N-methylglucamine. Among residues of easily cleavable esters which A may be are methoxymethyl, ethoxymethyl, isopropyloxymethyl, .alpha.-methoxyethyl, .alpha.-ethoxyethyl, methylthiomethyl, ethylthiomethyl, isopropylthiomethyl, pivaloyloxymethyl, acetoxymethyl, propionyloxymethyl, butyryloxymethyl, isobutyryloxymethyl, valeryloxymethyl, isovaleryloxymethyl, tert-butylcarbonyloxymethyl, hexadecanoyloxymethyl, propionyloxyethyl, isovaleryloxyethyl, 1-acetyloxyethyl, 1-propionyloxyethyl, 1-butyryloxyethyl, 1-tert-butylcarbonyloxyethyl, 1-acetyloxypropyl, 1-hexadecanoyloxyethyl, 1-propionyloxypropyl, 1-methoxycarbonyloxyethyl, methoxycarbonyloxymethyl, 1-acetyloxybutyl, 1-acetyloxyhexyl, 1-acetyloxyheptyl, phthalidyl, 5,6-dimethoxyphthalidyl, tert-butylcarbonylmethyl, allyl, 2-chloroallyl, methoxycarbonylmethyl, benzyl or tert-butyl.
Other residues of esters which A may be are: methoxyethoxymethyl, dimethylaminoethyl, cyanomethyl, tert-butyloxycarbonymethyl, 2,2-ethylenedioxyethyl, cyanoethyl, 2,2-dimethoxyethyl, 2-chloroethoxymethyl, 2-hydroxyethoxyethyl, 2,3-epoxypropyl, 3-dimethylamino, 2-hydroxypropyl, 2-hydroxyethyl, 2-methylaminoethoxymethyl, 2-amino-ethoxymethyl, 3-methoxy-2,4-thiadiazol-5-yl, 2-tetrahydropyranyl, 2-methoxyprop -2-yl, 1-hydroxy-prop-2yl, isopropyl, carbamoylmethyl, chloromethyl, 2-chloroethyl, acetylmethyl, 2-methylthioethyl or thiocyanatomethyl.
Other residues of ester groups which A may be are: 2-chloro-1-acetyloxyethyl, 2-bromo-1-acetyloxyethyl, 2-fluoro-1-acetyloxyethyl, 2-methoxy-1-acetyloxyethyl, 2-methyl-1-acetyloxypropyl, 2-acetyloxyprop-2-yl, 1-methoxyacetyloxyethyl, 1acetylcarbonyloxyethyl, 1-hydroxy-acetyloxyethyl, 1-formylcarbonyloxyethyl, 1-(2-thienyl)carbonyloxyethyl, 1-(2-furyl)carbonyloxyethyl, 1-(5-nitro-2-furyl)carbonyloxyethyl, 1-(2-pyrrolyl)carbonyloxyethyl, 1-(propionyloxycarbonyloxy)ethyl, 1-(propyloxycarbonyloxy)ethyl, 1-(isopropyloxycarbonyloxy)ethyl, 1-(methoxyethoxycarbonyloxy)ethyl, 1-(allyloxycarbonyloxy)ethyl, 1-(2,3-epoxy)propyloxycarbonyloxyethyl, 1-(2-furyl)methyloxycarbonyloxyethyl, 1-(2-fluoro)ethyloxycarbonyloxyethyl, 1-(methoxycarbonyloxy) propyl, (2-methoxycarbonyloxy)prop-2-yl, (methoxycarbonyloxy)-chloromethyl, 1-(methoxycarbonyloxy)-2-chloroethyl, 1-(methoxycarbonyloxy)-2-methoxyethyl, 1-(methoxycarbonyloxyl)-1-allyl. A may also be: ##STR29##
The products of formula I may also be in the form of salts of organic or mineral acids.
Among the acids with which the amino group or groups or the quaternary ammonium group can be salified, there can be mentioned, among others, the following acids: acetic acid, trifluoroacetic acid, maleic acid, tartaric acid, methanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, trifluoromethanesulfonic acid, formic acid, phosphoric acid, sulfuric acid, hydrochloric acid, hydrobromic acid, hydriodic acid. Among the values for A, the preferred esters have the formula ##STR30## in which B is hydrogen or optionally substituted linear or branched alkyl of 1 to 5 carbon atoms, and D is alkyl or alkoxy optionally substituted of 1 to 15 carbon atoms and particularly 1 to 5 carbon atoms, and more particularly the ester in which B is hydrogen or methyl or ethyl and D is methyl, ethyl, methoxy or ethoxy.
Among the values for A, there are ##STR31## in which Rx is hydrogen, alkyl, particularly methyl and ethyl, halogen, particularly chlorine, and Ry is hydrogen, halogen, aryl, particularly phenyl optionally substituted by methyl, methoxy or halogen, or Ry is alkyl optionally substituted by acyloxy, by alkoxycarbonyl or by halogen.
Among the values for A are ##STR32## in which Rx is defined as above and alk.sub.1 and alk .sub.2 are alkyl of 1 to 4 carbon atoms.
Among the compounds of formula I, a preferred group are the syn isomers of the formula ##STR33## in which R' is hydrogen or optionally substituted alkyl, alkenyl, alkynyl or cycloalkyl up to 6 carbon atoms or aryl, ZA has the value indicated above and R'.sub.3 A is phenyl, optionally substituted heterocyclic aryl, or optionally substituted quaternary ammonium, or acetyl or carbamoyl. ##STR34##
Among the products already mentioned of formula I.sub.A, the products are preferred in which R' is hydrogen, or methyl or isopropyl optionally substituted by carboxy, carbamoyl, nitrile, methylthio or methoxy, difluoromethyl or trifluoromethyl, phenyl, cyclobutyl, or cyclopropyl optionally substituted by carboxy, allyl optionally substituted by chlorine or bromine, and the products in which ZA is a simple bond and R'.sub.3 A is an optionally substituted pyridinium.
Among the preferred products are those described in the Examples, and particularly the following products:
the internal salt of (6S, 7S)7-�3-�7-��(2-amino-4-thiazolyl)-2-�Z-(di fluoromethoxy) iminoacetamido!-2-carboxy-8-oxo-4-thia 1-azabicyclo �4,2,0! oct-2-en-3yl!-2-(E)-propenyl-thieno �2,3-b! pyridinium; the internal salt of the syn isomer of (6S, 7S) 5-�3-�7-��(2-amino-4-thiazolyl) (methoxyimino) acetamido �2-carboxy-8-oxo 4-thia-1-azabicyclo �4,2,0! oct-2en-3yl!-2(E)-propenyl!-2-methyl-thiazolo �4,5-o!-pyridinium; the internal salt of (6S, 7S) 7-�3-�7-��(2-amino-4thiazolyl)-2-(Z)-(methoxyimino)-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl!propen-2-(E)-yl!-thieno-�2,3-b!-pyridinium;
The syn isomer of (6S, 7S) 7-��(2-amino 4-thiazolyl)-(methoxyimino) acetamido �3-��3-(1,3,4-thiadiazol-2-yl) thio!-1-(E)-propenyl!-8-oxo-4-thia-1azabicyclo-(4,2,0)oct-2-en-2-carboxylic acid; and the internal salt of the Z isomer (6S, 7S) 5-�3-�7-��(2-amino-4-thiazolyl)-(difluoromethoxy)imino-acetamidol-2-carboxy-8-oxo4-thia-1-azabicyclo-�4,2,0! oct-2-en-3-yl!-2-(E)-propenyl-�(2-methyl-thiazolo-�4,5-o!-pyridinium, 6S, 7S, .DELTA.Z 5-�3-�7-�(2-amino thiazol 4-yl)-(methoxyimino) acetamido! 2-carboxy-8-oxo-4-thia-1-azabyciclo �4,2,0! oct-2-en-3-yl! -2(E) propenyl! thiazolo �4,5-c!pyridinium, 6S, 7S syn isomer of 5-�3-�7-�(2-aminothiazol-4-yl) (difluoromethoxyimino) acetamido! 2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl!-2(E) propenyl!-thiazolo �4,5,c! pyridinium and 6S, 7S syn isomer of 7-�3-�7-(2-aminothiazol-4yl)(fluoromethoxyimino) acetamido! 2-carboxy-8-oxo--4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl! 2-(E) propenyl! thieno �2,3-b! pyridinium.
The process for the preparation of compounds of formula I comprises reacting a compound of the formula ##STR35## in which R.sub.4 and A have the significance indicated above and R.sub.A is either a free amino or one protected by a mono or divalent protector group, or R.sub.A is R, R having the significance indicated above, with a halogenation agent, or with a sulfonation agent then with triphenylphosphine, or by a reagent of the formula P (OAlk).sub.3 in which Alk is alkyl of 1 to 4 carbon atoms, to obtain either a product of the formula ##STR36## in which R.sub.A, R.sub.4 and A have the previous significance and X.sup.- is the residue of an anion, or a product of the formula ##STR37## in which R.sub.A, R.sub.4, A and Alk have the previous significance, which products of formulae VIII A or VIII'A, if desired, are treated first with a strong base then with an alkyl halide of the formula Hal--R".sub.A in which Hal is halogen and R".sub.A has the values of R'A other than hydrogen to obtain the products of the formulae ##STR38## wherein R'.sub.A has the significance indicated above, the products with the formulae VIII.sub.B or VIII'.sub.B representing the whole of the starting products VIII.sub.A or VIII'.sub.A and of products obtained after reacting said derivatives with a derivative of formula Hal--R".sub.A, which products of the formulae VIII.sub.B or VIII'.sub.B are treated with a product of the formula ##STR39## in which R'.sub.B has the value indicated above and Gp is a protector group of the hydroxyl to obtain a product of the formula ##STR40## in the form of a mixture of E and Z isomers or in the form of isomer E or Z, on which product of formula IX the following reations are carried out in any order whatsoever:
a) separation of the protector group Gp;
b) when R.sub.A is amino protected by amino- or divalent protector group, elimination of this protector group and treatment of product in which R.sub.A is amino either with an acid of the formula
RaCO.sub.2 H IVa
in which R.sub.a is an organic group or with a functional derivative of this acid, or with a product of the formula ##STR41## in which Ri and Rj have the significance indicated above and Xb is sulfur or oxygen or with a product of the formula
Rb-Xc IVc
in which Rb has the significance indicated above and Xc is halogen,
c) separation of the isomers E and Z to obtain a product of the formula ##STR42## in which R'.sub.B has the significance indicated above which product is reacted either with a reactive derivative of R.sub.3 A to obtain a product of the formula ##STR43## or with a derivative of an activation group of the hydroxyl then with a derivative or a reactive derivative of R.sub.3A to obtain a product of the formula ##STR44## or with a derivative of an activation group of the hydroxyl then with a product of the formula HS--R.sub.3A or a reactive derivative of this product to obtain a product of the formula ##STR45## which products of formulae XI.sub.A, XI.sub.B or XI.sub.C are submitted if necessary or if desired, to any one or more of the following reactions in any order whatsoever:
a) separation by hydrolysis, hydrogenolysis or by the action of thiourea of all or part of the protector group or groups.
b) esterification or salification with a base of the carboxy or sulfo group or groups.
c) salification with an acid of the aminos.
d) resolution of the molecule to obtain an optically active product.
e) oxication of the sulfur atom in position 2 of the isocephem ring.
The halogenation agent which is preferably used is thionyl chloride in a chlorinated solvent such as methylene chloride or in dimethylformamide. Then, intermediately, there is obtained a product of the formula ##STR46## There can also be used other halogenation reagents such as phosphorus pentachloride, phosphorus oxychloride or tosyl chloride. The sulfonation agent can be, for example, trifluoromethyl-sulfonic anhydride and the operation can then be done in the presence of a base, preferably in 2,6-dimethylpyridine or lutidine. In a general way, the sulfonation products are unstable and are not isolated.
The action of triphenylphosphine or of the reagent of the formula P(OAlk).sub.3 in which Alk is ethyl is carried out under the usual conditions. The action of triphenylphosphine or of the reagent with the formula P(OAlk).sub.3 is preferably carried out in the presence of silica on the halogenated product of formula VII.sub.a ; generally, the operation is done by heating to reflux a solvent such as toluene or chloroform. If a sulfonation agent is reacted on a product of formula VII, the action of triphenylphosphine or of the product with the formula P(OAlk).sub.3 is preferably carried out at the same time because of the instability of the sulfonation products.
The strong base with which the products of formulae VIII.sub.A and VIII'.sub.A are reacted may be chosen from potassium tert-butylate, lithium tert-butylate, lithium diisopropylamide, or lithium bis-trimethylsilyl amide. The alkyl halide of formula Hal.R"A is preferably the chloride or the bromide.
The action of the product of the formula ##STR47## on the products of formulae VIIIB or VIII'B is preferably carried out in a chlorinated solvent such as methylene chloride. The operation can be done in the presence of a relatively weak base such as triethylamine or DBU (1,8-diazabicyclo�5,4,0!undec-7 -ene), or DBM (1,5-diazabicyclo �4,3,0!non-5-ene), preferably at ambient temperature or by heating. It is equally possible to operate in the presence of a strong base such as tert-butyl lithium or an alkali metal alcoholate such as lithium tert-butylate, lithium bistrimethylsilyl amide or lithium diisopropyl-amide. The operation is then done at a low temperature, such as from -70.degree. C. to ambient temperature.
The protector group which Gp is may be a silyl such as trimethylsilyl or tert-butyl-dimethylsilyl although a group such as tetrahydropyranyl can be used. The separation of the protection group Gp is carried out under standard conditions such as in the presence of an acid or a fluoride ion from hydrofluoric acid or tetrabutylammonium fluoride.
When a product of formula IX is obtained in which R.sub.a is amino, in a preferred way of carrying out the process, the product of formula IX is treated with a fuctional derivative of a product of formula IV.sub.a which may be a halide, a symmetrical or mixed anhydride, an amide or as activated ester.
An example of a mixed anhydride is that of isobutyl chloroformate and pivaloyl chloride and carboxylic-sulfonic mixed anhydrides formed for example with p-toluenesulfonyl chloride. As an example of an activated ester, the ester formed with 2,4-dinitrophenol and the one formed with hydroxybenzothiazole may be mentioned.
As an example of a halide, the chloride or the bromide can be cited. There can equally be cited the acid azide or the acid amide. The anhydride can be formed in situ by the action of disubstituted NN' carbodiimide, for example, N,N-dicyclohexylcarbodiimide.
The acylation reaction is preferably carried out in an organic solvent such as methylene chloride but other solvents such as tetra-hydrofuran, chloroform or dimethylformamide may be used.
When an acid halide is used, generally when a molecule of a hydrohalide acid is liberated during a reaction, the reaction is preferably carried out in the presence of a base such as sodium hydroxide, potassium hydroxide, the carbonates and bicarbonates of sodium or potassium, sodium acetate, triethylamine, pyridine, morpholine or N-methylmorpholine. The reaction temperature is generally lower than or equal to ambient temperature.
In a preferred way of carrying out the process, the products of formula IV.sub.b are converted into reactive derivatives such as the halides of acids, which can be prepared by reacting the products of formula IV.sub.b with a halogenation agent such as phosgene, oxalyl chloride, thionyl chloride. There can also be prepared complexes with dialkyl sulfates, preferably dimethyl sulfate. The operating condition for such reactions are known to one skilled in the art and such reactions are described, for example, in French Patent No. 2,073,338.
In a preferred way of carrying out the process, the halogens used in the products of formula IV.sub.C are the chloride or the fluoride. It is preferred to use a pyridinium derivative and the counterion is then preferably an iodide, tosylate, bromide, or BF4 ion. The preparation of the products of formula IV.sub.C and the reaction of these products with the products of formula IX are carried out under the conditions described for example in Journal of Medicinal Chemistry (1982) Vol. 25, No. 4, p. 457-469. The subsequent reaction, if required, of separation of the E and Z isomers is carried out according to the usual techniques but it is preferred to use chromatography over silica. The conversion of the products of formula X into products of formula XI.sub.A is also done by standard methods.
The derivative of R.sub.3 A which is used can, for example be a halide derived from a carbocylic aryl or heterocyclic aryl optionally substituted. Preferably, the fluoride is then used when R.sub.3 A is for example, acetyl or carbamoyl and it is preferred to operate in the presence of a reactive derivative such as an anhydride or a halide.
The conversion of the products of formula X into products of formula XI B is preferably carried out under the following conditions: an activated derivative of the hydroxyl is prepared by the action, for example, of a derivative of a sulfonic acid such as the anhydride of trifluoromethylsulfonic acid and is done at low temperatures to ambient temperature. When R.sub.3 A is not a quaternary ammonium, it is preferred to operate in the presence of a base.
The conversion of the products of formula X into products of formula XI.sub.C is carried out under similar condition. First, an activated derivative of the hydroxyl is prepared under the previously stated conditions, particularly starting with the anhydride of trifluoromethylsulfonic acid. The action of the product of formula HS-R.sub.3A is preferably carried out in the presence of an organic base such as 2,6-dimethylpyridine and of a soluble iodide source and it is then preferred to operate in the presence of tetra-alkylammonium iodide.
The products of formulae XI.sub.A, XI.sub.B and XI.sub.C constitute products of formula I.sub.A when they do not include any protective group and when A is not among the easily cleavable ester groups, one of those which it is desired to eliminate.
In other cases. the action on the products of formula XI.sub.A, XI.sub.B or XI.sub.C of one or more hydrolysis or hydrogenolysis agents or of thiourea has the object of eliminating the protective group or groups which the different products may contain. The nature of the reagents to react in all these cases is well known to an expert. Examples of such reactions are given further on in the experimental part. A non-exhaustive list of the means which can be used to eliminate the different groups in now given.
The elimination of the protector group or groups may be done by hydrolysis, with an acid, base, or by using hydrazine. It is preferred to use acid hydrolysis to eliminate optionally substituted alkoxy and cycloalkycarbonyl such as tert-pentyloxycarbonyl or tert-butyloxycarbonyl, optionally substituted aralkoxycarbonyl such as benzyloxycarbonyl, and trityl, benzhydryl, tert-butyl or 4-methoxybenzyl. The acid which is preferably utilized can be selected from the group consisting of hydrochloric acid, benzene sulfonic acid or p-toluene-sulfonic acid, formic acid or trifluoroacetic acid. Other mineral or organic acids can however be used.
Basic hydrolysis is preferably used to eliminate acyls such as trifluoroacetyl. The base which is preferably used is an inorganic base such as sodium or potassium hydroxide but also useful are magnesia, baryta, or an alkali metal carbonate or bicarbonate such as the carbonates and bicarbonates of sodium or potassium or other bases. Sodium or potassium acetate can also be used. Hydrolysis using hydrazine is used preferably to eliminate groups such as phthaloyl.
Certain groups can also be eliminated by a zinc-acetic acid system for trichloroethyl. Benzhydryl and benzyloxycarbonyl are preferably elimated by hydrogen in the presence of a catalyst. The chloroacetyl group is eliminated by the action of thiourea in a neutral or acid medium according to the type of reaction described by MASAKI, J.A.C.S., 90, 4508, (1968). Other methods of deprotection known in the literature can also be used.
Among the preferred groups are formyl, acetyl, ethoxycarbonyl, mesyl, trifluoroacetyl, chloroacetyl, trityle with trityl and chloroacetyl being particularly preferred. The acid preferably used is trifluoro-acetic acid.
Salification of the products can be carried out by the usual methods. Salification can, for example, be obtained by action on a product in the form of an acid or on a solvate, for example the ethanol solvate or a hydrate of this acid of a mineral base such as sodium or potassium hydroxide, the carbonate or bicarbonate of sodium or potassium. There can also be used the salts of mineral acids such as the tri-sodium phosphate. Use can also be made of salts of organic acids.
Salts of organic acids are for example, the sodium salts of aliphatic carboxylic acids, linear or branched, saturated or unsaturated of 1 to 18, and preferably of 2 to 10, carbon atoms. These aliphatic radicals can be interrupted by one or more heteroatoms such as oxygen or sulfur, or can be substituted by aryl, such as, for example: phenyl, thienyl, furyl: or by one or more hydroxyl or by one or more halogens such as fluorine, chlorine or bromine, preferably chlorine; by one or more lower carboxylic or alkoxycarbonyl, preferably methoxycarbonyl, ethoxycarbonyl or propyloxycarbonyl; by one or more aryloxy, preferably phenoxy.
Furthermore, there can be used as organic acids the sufficiently soluble aromatic acids such, for example, as benzoic acids preferably substituted by lower alkyl radicals. Examples of such organic acids are formic acid, acetic acid, acrylic acid, butyric acid, adipic acid isobutyric acid, n-caproic acid, isocaproic acid, chloropropionic acid, crotonic acid, phenylacetic acid, 2-thienylacetic acid, 3-thienylacetic acid, 4-ethylphenylacetic acid, glutaric acid, the monoethyl ester of adipic acid; the following acids: hexanoic acid, heptanoic acid, decanoic acid, oleic acid, stearic acid, palmitic acid, 3-hydroxypropionic acid, 3-methoxypropionic acid, 3-methylthiobutyric acid, 4-chlorobutyric acid, 4-phenylbutyric acid, 3-phenoxybutyric acid, 4-ethylbenzoic, 1-propylbenzoic acid. However, it is preferred to use as salts of sodium, the acetate, the 2-ethylhexanoate or the diethylacetate.
Salification can also be obtained by the action of an organic base such as triethylamine, diethylamine, trimethylamine, propylamine, N,N-dimethylethanolamine, tris(hydroxymethyl)amino methane, methylamine, ethanolamine, pyridine, picoline, dicyclohexylamine, morpholine and benzylamine. It can also be obtained by the action of arginine, of lysine, of procaine, of histidine and of N-methyl glucamine. This salification is preferably carried out in a solvent or a mixture of solvents such as water, ethyl ether, methanol, ethanol or acetone.
The salts are obtained in an amorphous or crystallized form according to the reaction conditions employed. Crystallized salts are preferably prepared by reacting the free acids with one of the salts of aliphatic carboxylic acids mentioned above, preferably with sodium acetate. The salification of the products by mineral or organic acids is carried out in the usual conditions.
The eventual esterification of the products is carried out under standard conditions. In general, the operation is effected by reacting the acid of formula I with a derivative of the formula
Z--R.sub.S
in which Z is a hydroxyl or halogen such as chlorine, bromine or iodine, and R.sub.S is the ester group to be introduced, of which groups a non-exhaustive list appears above. In certain cases, it is advantageous to carry out an esterification on a product of which the amine is blocked before removing the protector group of the amine.
The possible resolution of the compounds of formulae XI.sub.A, XI.sub.B and XI.sub.C can be carried out with an optically active carboxylic or sulfonic acid such as tartaric acid, dibenzoyltartaric acid, campho-sulfonic acid or glutamic acid, the decomposition of the salt so obtained being effected with a mineral base such as sodium bicarbonate or an organic base such as a tertiary amine such as triethylamine. In addition, there can also be used an optically active base.
The possible oxidation of the products of formulae XI.sub.A, XI.sub.B, or XI.sub.C can be carried out with oxygen, peroxides, hydroperoxides, peracids or hydrogen peroxide and the reaction is advantageously sensitized by light. These reagents can be mixed with organic or mineral acids and it is preferred to use m-chloroperbenzoic acid. The reaction conditions are known to an expert such as are set out, for example, in French patent No. 2,387,234.
The novel antibiotic compositions of the invention are comprised of an antibiotically effective amount of at least one compound of formula I and their non-toxic, pharmaceutically acceptable acid addition salts and an inert pharmaceutical carrier or excipient. The compositions may be in the form of tablets, dragees, capsules, granules, suppositories, ointments, creams, gels and injectable solutions or suspensions.
Examples of suitable excipients are talc, gum arabic, lactose, starch, magnesium stearate, cocoa butter, aqueous and non-aqueous vehicles, fatty substances of animal or vegetable origin, paraffin derivatives, glycols, various wetting, dispersing or emulsifying agents and preservatives. Preferably, the compositions are in the form of a powder capable of extemporaneously dissolving in an appropriate vehicle such as apyrogenous sterile water.
The compositions of the invention have an excellent anti-bacterial activity against gram (+) bacterial such as staphylococci, streptococci and especially penicillin resistant staphylococci. Their effectiveness on the gram (-) bacteria, particularly on coliform, klebsiella, salmonella and proteus bacteria is particularly notable.
These compositions are useful in the treatment of infections by sensitive germs and, notably, of staphylococci such as septicemias by staphylococci, malignant staphylococcal infection of the face or cutaneous, pyodermitis, septic or suppurating wounds, anthrax, phlegmons, erysipelas, acute primitive or post-influenzal staphyloccocia, bronchopneumonia and pulmonary suppuration. The compositions are useful in the treatment of colibacilloses and associated infections, in infections due to proteus, klebsiella and salmonella and in other affections caused by gram (-) bacteria or for disinfecting surgical instruments.
In a preferred mode, the compositions contain as the active ingredient a compound of formula ##STR48## syn isomer, in which R' is hydrogen or alkyl, alkenyl or alkynyl or cycloalkyl with up to 6 carbon atoms, optionally substituted, or aryl, ZA has the values indicated above and R'.sub.3 A is phenyl, heterocyclic aryl optionally substituted or quaternary ammonium optionally substituted or acetyle or carbaloyl.
Particularly preferred compositions are those of formula I.sub.A in which R' is hydrogen, or methyl or isopropyl optionally substituted by carboxy, carbamoyl, nitrile, methylthio or methoxy, difluoromethyl or trifluoromethyl, phenyl, cyclobutyl or cyclopropyl optionally substituted by carboxy, allyl optionally substituted by chlorine or bromine and ZA is a simple bond and R'.sub.3 A an optionally substituted pyridinium.
The novel method of the invention of combatting bacterial infections in warm-blooded animals, including humans, comprises administering to warm-blooded animals an antibactericidally effective amount of at least one compound of formula I and their non-toxic, pharmaceutically acceptable acid addition salts. The compounds may be administered orally, rectally, parenterally or topically to the skin or mucous. The usual daily dose is depending on the condition treated, the specific compound and the method of administration. For example, the products of Examples 1, 2, 47 and 51 may be administered intramuscularly at a dose of 6,5 to 13 mg/kg three times a day. When administered orally, it is preferably an easily cleavable ester such as propionyloxymethyl.

The products of formula VII used as starting materials may be prepared by the process of French Patent No. 2,559,486 as illustrated in the examples below.
Examples of products of the formula ##STR49## wherein R.sub.1, R.sub.1A, A and n.sub.2 have the above definitions are illustrated in the following Tables.
- R R.sub.1A n.sub.2 CO.sub.2 A R R.sub.1A n.sub.2 CO.sub.2 A ##STR50## ##STR51## O CO.sub.2.sup..crclbar. ##STR52## ##STR53## O CO.sub.2.sup..crclbar. " ##STR54## " " " ##STR55## " CO.sub.2 H " ##STR56## " " " ##STR57## " " " ##STR58## " " " ##STR59## " CO.sub.2.sup..crclbar. " ##STR60## " " " ##STR61## " " " ##STR62## " " " ##STR63## " " " ##STR64## " " " ##STR65## " " " ##STR66## " " " ##STR67## " " " ##STR68## " " " ##STR69## " " " ##STR70## " CO.sub.2 H " ##STR71## " " ##STR72## ##STR73## O CO.sub.2.sup..crclbar. ##STR74## ##STR75## O CO.sub.2.sup..crclbar. " ##STR76## " " " ##STR77## " " " ##STR78## " " " ##STR79## " " " ##STR80## " " " ##STR81## " " " ##STR82## " " " ##STR83## " " " ##STR84## " " " ##STR85## " " " ##STR86## " " " ##STR87## " " " ##STR88## " " " ##STR89## " " " ##STR90## " " " ##STR91## " " " ##STR92## " " " ##STR93## " " ##STR94## ##STR95## O CO.sub.2.sup..crclbar. ##STR96## ##STR97## O CO.sub.2.sup..crclbar. " ##STR98## " " " ##STR99## " " " ##STR100## " " " ##STR101## " " " ##STR102## " " " ##STR103## " " " ##STR104## " " " ##STR105## " " " ##STR106## " " " ##STR107## " " " ##STR108## " " " ##STR109## " " " ##STR110## " " " ##STR111## " " " ##STR112## " " " ##STR113## " CO.sub.2 H " ##STR114## " CO.sub.2 H " ##STR115## " " ##STR116## ##STR117## O CO.sub.2.sup..crclbar. ##STR118## ##STR119## O CO.sub.2.sup..crclbar. " ##STR120## " " " ##STR121## " " " ##STR122## " " " ##STR123## " " " ##STR124## " " " ##STR125## " " " ##STR126## " " " ##STR127## " " " ##STR128## " " " ##STR129## " " " ##STR130## " " " ##STR131## " " " ##STR132## " " " ##STR133## " " " ##STR134## " " " ##STR135## " " " ##STR136## " " " ##STR137## " " ##STR138## ##STR139## O CO.sub.2.sup..crclbar. ##STR140## ##STR141## O CO.sub.2.sup..crclbar. " ##STR142## " " " ##STR143## " " " ##STR144## " " " ##STR145## " " " ##STR146## " " " ##STR147## " " " ##STR148## " " " ##STR149## " " " ##STR150## " " " ##STR151## " " " ##STR152## " " " ##STR153## " " " ##STR154## " " " ##STR155## " " " ##STR156## " " " ##STR157## " " " ##STR158## " " " ##STR159## " " ##STR160## ##STR161## O CO.sub.2.sup..crclbar. ##STR162## ##STR163## O CO.sub.2.sup..crclbar. " ##STR164## " " " ##STR165## " " " ##STR166## " " " ##STR167## " " " ##STR168## " " " ##STR169## " " " ##STR170## " " " ##STR171## " " " ##STR172## " " " ##STR173## " " " ##STR174## " " " ##STR175## " " " ##STR176## " " " ##STR177## " " " ##STR178## " " " ##STR179## " " " ##STR180## " " " ##STR181## " " ##STR182## ##STR183## O CO.sub.2.sup..crclbar. ##STR184## ##STR185## O CO.sub.2.sup..crclbar. " ##STR186## " " " ##STR187## " " " ##STR188## " " " ##STR189## " " ##STR190## " " " ##STR191## " " " ##STR192## " " " ##STR193## " " " ##STR194## " " " ##STR195## " " " ##STR196## " " " ##STR197## " " " ##STR198## " " " ##STR199## " " " ##STR200## " " " ##STR201## " " " ##STR202## " " " ##STR203## " " ##STR204## ##STR205## O CO.sub.2.sup..crclbar. ##STR206## ##STR207## O CO.sub.2.sup..crclbar. " ##STR208## " " " ##STR209## " " " ##STR210## " " " ##STR211## " " " ##STR212## " " " ##STR213## " " " ##STR214## " " " ##STR215## " " " ##STR216## " " " ##STR217## " " " ##STR218## " " " ##STR219## " " " ##STR220## " " " ##STR221## " " " ##STR222## " " " ##STR223## " " " ##STR224## " " " ##STR225## " " ##STR226## ##STR227## O CO.sub.2 H ##STR228## ##STR229## O CO.sub.2 H " ##STR230## " " " ##STR231## " " " ##STR232## " " " ##STR233## " " " ##STR234## " " " ##STR235## " " " ##STR236## " " " ##STR237## " " " ##STR238## " CO.sub.2.sup..crclbar. " ##STR239## " " " ##STR240## " CO.sub.2 H " ##STR241## " " " ##STR242## " " " ##STR243## " " " ##STR244## " " " ##STR245## " " " ##STR246## " " " ##STR247## " " ##STR248## ##STR249## O CO.sub.2 H ##STR250## ##STR251## O CO.sub.2 H " ##STR252## " " " ##STR253## " " " ##STR254## " " " ##STR255## " " " ##STR256## " " " ##STR257## " " " ##STR258## " " " ##STR259## " " " ##STR260## " " " ##STR261## " " " ##STR262## " " " ##STR263## " " " ##STR264## " " " ##STR265## " " " ##STR266## " " " ##STR267## " " " ##STR268## " " " ##STR269## " " ##STR270## ##STR271## O CO.sub.2 H ##STR272## ##STR273## O CO.sub.2 H " ##STR274## " " " ##STR275## " " " ##STR276## " " " ##STR277## " " " ##STR278## " " " ##STR279## " " " ##STR280## " " " ##STR281## " " " ##STR282## " " " ##STR283## " " " ##STR284## " " " ##STR285## " " " ##STR286## " " " ##STR287## " " " ##STR288## " " " ##STR289## " " " ##STR290## " " " ##STR291## " " ##STR292## ##STR293## O CO.sub.2 H ##STR294## ##STR295## O CO.sub.2 H " ##STR296## " " " ##STR297## " " " ##STR298## " " " ##STR299## " " " ##STR300## " " " ##STR301## " " " ##STR302## " " " ##STR303## " " " ##STR304## " " " ##STR305## " " " ##STR306## " " " ##STR307## " " " ##STR308## " " " ##STR309## " " " ##STR310## " " " ##STR311## " " " ##STR312## " " " ##STR313## " " ##STR314## ##STR315## O CO.sub.2 H ##STR316## ##STR317## O CO.sub.2 H " ##STR318## " " " ##STR319## " CO.sub.2.sup..crclbar. " ##STR320## " " " ##STR321## " CO.sub.2 H " ##STR322## " " " ##STR323## " " " ##STR324## " " " ##STR325## " " " ##STR326## " " " ##STR327## " " " ##STR328## " " " ##STR329## " " " ##STR330## " " " ##STR331## " " " ##STR332## " " " ##STR333## " " " ##STR334## " " " ##STR335## " " ##STR336## ##STR337## O CO.sub.2 H ##STR338## ##STR339## O CO.sub.2 H " ##STR340## " " " ##STR341## " " " ##STR342## " " " ##STR343## " " " ##STR344## " " " ##STR345## " " " ##STR346## " " " ##STR347## " " " ##STR348## " " " ##STR349## " " " ##STR350## " " " ##STR351## " " " ##STR352## " " " ##STR353## " " " ##STR354## " " " ##STR355## " " " ##STR356## " " " ##STR357## " " ##STR358## ##STR359## O CO.sub.2 H ##STR360## ##STR361## O CO.sub.2 H " ##STR362## " " " ##STR363## " " " ##STR364## " " " ##STR365## " " " ##STR366## " " " ##STR367## " " " ##STR368## " " " ##STR369## " " " ##STR370## " " " ##STR371## " " " ##STR372## " " " ##STR373## " " " ##STR374## " " " " " " ##STR375## " " " " " " ##STR376## " " " " " ##STR377## ##STR378## O CO.sub.2.sup..crclbar. ##STR379## ##STR380## O CO.sub.2.sup..crclbar. " ##STR381## " " " ##STR382## " " " ##STR383## " " " ##STR384## " " " ##STR385## " " " ##STR386## " " " ##STR387## " " " ##STR388## " " " ##STR389## " " " ##STR390## " " " ##STR391## " " " ##STR392## " " " ##STR393## " " " ##STR394## " " " ##STR395## " " " ##STR396## " " " ##STR397## " CO.sub.2 H " ##STR398## " CO.sub.2 H ##STR399## ##STR400## O CO.sub.2.sup..crclbar. ##STR401## ##STR402## O CO.sub.2.sup..crclbar. " ##STR403## " " " ##STR404## " " " ##STR405## " " " ##STR406## " " ##STR407## " " " ##STR408## " " " ##STR409## " " " ##STR410## " " " ##STR411## " " " ##STR412## " " " ##STR413## " " " ##STR414## " " " ##STR415## " " " ##STR416## " " " ##STR417## " " " ##STR418## " " " ##STR419## " " " ##STR420## " " ##STR421## ##STR422## O CO.sub.2.sup..crclbar. ##STR423## ##STR424## O CO.sub.2.sup..crclbar. " ##STR425## " " " ##STR426## " " " ##STR427## " " " ##STR428## " " " ##STR429## " " " ##STR430## " " " ##STR431## " " " ##STR432## " " " ##STR433## " " " ##STR434## " " " ##STR435## " " " ##STR436## " " " ##STR437## " " " ##STR438## " " " ##STR439## " " " ##STR440## " " " ##STR441## " " " ##STR442## " " ##STR443## ##STR444## O CO.sub.2.sup..crclbar. ##STR445## ##STR446## O CO.sub.2.sup..crclbar. " ##STR447## " " " ##STR448## " " " ##STR449## " " " ##STR450## " " " ##STR451## " " " ##STR452## " " " ##STR453## " " " ##STR454## " " " ##STR455## " " " ##STR456## " " " ##STR457## " " " ##STR458## " " " ##STR459## " " " ##STR460## " " " ##STR461## " " " ##STR462## " " " ##STR463## " " " ##STR464## " " ##STR465## ##STR466## O CO.sub.2.sup..crclbar. ##STR467## ##STR468## O CO.sub.2.sup..crclbar. " ##STR469## " " " ##STR470## " " ##STR471## " " " ##STR472## " " " ##STR473## " " " ##STR474## " " " ##STR475## " " " ##STR476## " " " ##STR477## " " " ##STR478## " " " ##STR479## " " " ##STR480## " " " ##STR481## " " " ##STR482## " " " ##STR483## " " " ##STR484## " " " ##STR485## " " " ##STR486## " " ##STR487## ##STR488## O CO.sub.2.sup..crclbar. ##STR489## ##STR490## O CO.sub.2.sup..crclbar. " ##STR491## " " " ##STR492## " " " ##STR493## " " " ##STR494## " " " ##STR495## " " " ##STR496## " " " ##STR497## " " " ##STR498## " " " ##STR499## " " " ##STR500## " " " ##STR501## " " " ##STR502## " " " ##STR503## " " " ##STR504## " " " ##STR505## " " " ##STR506## " " " ##STR507## " " " ##STR508## " " ##STR509## ##STR510## O CO.sub.2.sup..crclbar. ##STR511## ##STR512## O CO.sub.2.sup..crclbar. " ##STR513## " " " ##STR514## " " " ##STR515## " " " ##STR516## " " " ##STR517## " " " ##STR518## " " " ##STR519## " " " ##STR520## " " " ##STR521## " " " ##STR522## " " " ##STR523## " " " ##STR524## " " " ##STR525## " " " ##STR526## " " " ##STR527## " " " ##STR528## " " " ##STR529## " " " ##STR530## " " ##STR531## ##STR532## O CO.sub.2.sup..crclbar. ##STR533## ##STR534## O CO.sub.2.sup..crclbar. " ##STR535## " " " ##STR536## " " " ##STR537## " " " ##STR538## " " " ##STR539## " " " ##STR540## " " " ##STR541## " " " ##STR542## " " " ##STR543## " " " ##STR544## " " " ##STR545## " " " ##STR546## " " " ##STR547## " " " ##STR548## " " " ##STR549## " " " ##STR550## " " " ##STR551## " " " ##STR552## " " ##STR553## ##STR554## O CO.sub.2.sup..crclbar. ##STR555## ##STR556## O CO.sub.2.sup..crclbar. " ##STR557## " " " ##STR558## " " " ##STR559## " " " ##STR560## " " " ##STR561## " " " ##STR562## " " " ##STR563## " " " ##STR564## " " " ##STR565## " " " ##STR566## " " " ##STR567## " " " ##STR568## " " " ##STR569## " " " ##STR570## " " " ##STR571## " " " ##STR572## " " " ##STR573## " " " ##STR574## " " ##STR575## ##STR576## O CO.sub.2.sup..crclbar. ##STR577## ##STR578## O CO.sub.2.sup..crclbar. " ##STR579## " " " ##STR580## " " " ##STR581## " " " ##STR582## " " " ##STR583## " " " ##STR584## " " " ##STR585## " " " ##STR586## " " " ##STR587## " " " ##STR588## " " " ##STR589## " " " ##STR590## " " " ##STR591## " " " ##STR592## " " " ##STR593## " " " ##STR594## " " " ##STR595## " " " ##STR596## " " ##STR597## ##STR598## O CO.sub.2.sup..crclbar. ##STR599## ##STR600## O CO.sub.2.sup..crclbar. " ##STR601## " " " ##STR602## " " " ##STR603## " " " ##STR604## " " " ##STR605## " " " ##STR606## " " " ##STR607## " " " ##STR608## " " " ##STR609## " " " ##STR610## " " " ##STR611## " " " ##STR612## " " " ##STR613## " " " ##STR614## " " " ##STR615## " " " ##STR616## " " " ##STR617## " " " ##STR618## " " ##STR619## ##STR620## O CO.sub.2.sup..crclbar. ##STR621## ##STR622## O CO.sub.2.sup..crclbar. " ##STR623## " " " ##STR624## " " " ##STR625## " " " ##STR626## " " ##STR627## " " " ##STR628## " " " ##STR629## " " " ##STR630## " " " ##STR631## " " " ##STR632## " " " ##STR633## " " " ##STR634## " " " ##STR635## " " " ##STR636## " " " ##STR637## " " " ##STR638## " " " ##STR639## " " " ##STR640## " " ##STR641## ##STR642## O CO.sub.2.sup..crclbar. ##STR643## ##STR644## O CO.sub.2.sup..crclbar. " ##STR645## " " " ##STR646## " " " ##STR647## " " " ##STR648## " " " ##STR649## " " " ##STR650## " " " ##STR651## " " " ##STR652## " " " ##STR653## " " " ##STR654## " " " ##STR655## " " " ##STR656## " " " ##STR657## " " " ##STR658## " " " ##STR659## " " " ##STR660## " " " ##STR661## " " " ##STR662## " " ##STR663## ##STR664## O CO.sub.2.sup..crclbar. ##STR665## ##STR666## O CO.sub.2 H " ##STR667## " CO.sub.2 H " ##STR668## " CO.sub.2.sup..crclbar. " ##STR669## " CO.sub.2.sup..crclbar. " ##STR670## " " " ##STR671## " " " ##STR672## " " " ##STR673## " " " ##STR674## " " " ##STR675## " " " ##STR676## " " " ##STR677## " " " ##STR678## " " " ##STR679## " " " ##STR680## " " " ##STR681## " " " ##STR682## " " " ##STR683## " CO.sub.2 H " ##STR684## " CO.sub.2 H ##STR685## ##STR686## O CO.sub.2.sup..crclbar. ##STR687## ##STR688## O CO.sub.2.sup..crclbar. " ##STR689## " " " ##STR690## " " " ##STR691## " " " ##STR692## " " " ##STR693## " " " ##STR694## " " " ##STR695## " " " ##STR696## " " " ##STR697## " " " ##STR698## " " " ##STR699## " " " ##STR700## " " " ##STR701## " " " ##STR702## " " " ##STR703## " " " ##STR704## " " " ##STR705## " CO.sub.2 H " ##STR706## " " ##STR707## ##STR708## O CO.sub.2.sup..crclbar. ##STR709## ##STR710## O CO.sub.2.sup..crclbar. " ##STR711## " " " ##STR712## " " " ##STR713## " " " ##STR714## " " ##STR715## " " " ##STR716## " " " ##STR717## " " " ##STR718## " " " ##STR719## " " " ##STR720## " " " ##STR721## " " " ##STR722## " " " ##STR723## " " " ##STR724## " " " ##STR725## " " " ##STR726## " " " ##STR727## " " " ##STR728## " " ##STR729## ##STR730## O CO.sub.2.sup..crclbar. ##STR731## ##STR732## O CO.sub.2.sup..crclbar. " ##STR733## " " " ##STR734## " " " ##STR735## " " " ##STR736## " " ##STR737## " CO.sub.2 H " ##STR738## " " " ##STR739## " CO.sub.2.sup..crclbar. 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" ##STR1288## " " " ##STR1289## " " " ##STR1290## " " " ##STR1291## " " " ##STR1292## " " " ##STR1293## " CO.sub.2 H " ##STR1294## " " " ##STR1295## " " ##STR1296## ##STR1297## O CO.sub.2.sup..crclbar. ##STR1298## ##STR1299## O CO.sub.2.sup..crclbar. " ##STR1300## " " " ##STR1301## " " " ##STR1302## " " " ##STR1303## " " " ##STR1304## " " " ##STR1305## " " " ##STR1306## " " " ##STR1307## " " ##STR1308## ##STR1309## O CO.sub.2.sup..crclbar. ##STR1310## ##STR1311## O CO.sub.2 H " ##STR1312## " " " ##STR1313## " " " ##STR1314## " " " ##STR1315## " " " ##STR1316## " CO.sub.2 H " ##STR1317## " CO.sub.2.sup..crclbar. " ##STR1318## " " " ##STR1319## " " ##STR1320## ##STR1321## O CO.sub.2.sup..crclbar. ##STR1322## ##STR1323## O CO.sub.2.sup..crclbar. " ##STR1324## " " " ##STR1325## " " " ##STR1326## " " " ##STR1327## " " " ##STR1328## " " " ##STR1329## " " " ##STR1330## " " " ##STR1331## " " ##STR1332## ##STR1333## O CO.sub.2.sup..crclbar. ##STR1334## ##STR1335## O CO.sub.2 H " ##STR1336## " " " ##STR1337## " " " ##STR1338## " " " ##STR1339## " " " ##STR1340## " CO.sub.2 H " ##STR1341## " CO.sub.2.sup..crclbar. " ##STR1342## " " " ##STR1343## " " ##STR1344## ##STR1345## O CO.sub.2.sup..crclbar. ##STR1346## ##STR1347## O CO.sub.2.sup..crclbar. " ##STR1348## " " " ##STR1349## " " " ##STR1350## " " " ##STR1351## " " " ##STR1352## " CO.sub.2 H " ##STR1353## " " " ##STR1354## " " " ##STR1355## " " ##STR1356## ##STR1357## O CO.sub.2.sup..crclbar. ##STR1358## ##STR1359## O CO.sub.2.sup..crclbar. " ##STR1360## " " " ##STR1361## " " " ##STR1362## " " " ##STR1363## " " " ##STR1364## " " " ##STR1365## " CO.sub.2 H " ##STR1366## " " " ##STR1367## " " ##STR1368## ##STR1369## O CO.sub.2.sup..crclbar. ##STR1370## ##STR1371## O CO.sub.2.sup..crclbar. " ##STR1372## " " " ##STR1373## " " " ##STR1374## " " " ##STR1375## " " " ##STR1376## " " " ##STR1377## " " " ##STR1378## " " " ##STR1379## " " ##STR1380## ##STR1381## O CO.sub.2.sup..crclbar. ##STR1382## ##STR1383## O CO.sub.2 H " ##STR1384## " " " ##STR1385## " " " ##STR1386## " " " ##STR1387## " " " ##STR1388## " CO.sub.2 H " ##STR1389## " CO.sub.2.sup..crclbar. " ##STR1390## " " " ##STR1391## " " ##STR1392## ##STR1393## O CO.sub.2.sup..crclbar. ##STR1394## ##STR1395## O CO.sub.2.sup..crclbar. " ##STR1396## " " " ##STR1397## " " " ##STR1398## " " " ##STR1399## " " " ##STR1400## " " " ##STR1401## " " " ##STR1402## " " " ##STR1403## " " ##STR1404## ##STR1405## O CO.sub.2.sup..crclbar. ##STR1406## ##STR1407## O CO.sub.2 H " ##STR1408## " " " ##STR1409## " " " ##STR1410## " " " ##STR1411## " " " ##STR1412## " CO.sub.2 H " ##STR1413## " CO.sub.2.sup..crclbar. " ##STR1414## " " " ##STR1415## " " ##STR1416## ##STR1417## O CO.sub.2.sup..crclbar. ##STR1418## ##STR1419## O CO.sub.2.sup..crclbar. " ##STR1420## " " " ##STR1421## " " " ##STR1422## " " " ##STR1423## " " " ##STR1424## " CO.sub.2 H " ##STR1425## " " " ##STR1426## " " " ##STR1427## " " ##STR1428## ##STR1429## O CO.sub.2.sup..crclbar. ##STR1430## ##STR1431## O CO.sub.2.sup..crclbar. 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REFERENCE EXAMPLE A
Syn isomer of cis racemic 7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-4-thia-3-methoxymethyl-1-azabicyclo�4,2,0!-oct-2-en-2-carboxylic acid
STEP A: Methoxyacetaldehyde
100 ml of dimethyl ketal of methoxyactaldehyde, 100 ml of water and 3.2 ml of concentrated hydrochloric acid were refluxed and then several fractional distillations were carried out to obtain 8.7 g of methoxyacetaldehyde.
STEP B: 1,1-dimethylethyl 2-chloro-3-methoxymethyloxirane-carboxylate
A mixture of 2.106 g of methoxyacetaldehyde, 3.8 ml of tertbutyl dichloroacetate and 25 ml of tetrahydrofuran was cooled to -20.degree. C. and over 15 minutes, 29 ml of potassium tertbutylate in tetrahydrofuran (0.9M) were introduced. The mixture stood for 20 minutes and 25 ml of ether and 25 ml of water were added. The mixture was extracted with ether and the organic phase was washed with water saturated with sodium chloride, then dried and concentrated to dryness under reduced pressure. The residue was chromatographed over silica and eluted with methylene chloride to obtain 1.44 g of 1,1-dimethylethyl 2-chloro-3-methoxymethyloxirane-carboxylate.
STEP C: 1,1-dimethyethyl 7-�2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-2-hydroxy-3-methoxymethyl-4-thia-1-azabicyclo �4,2,0!octane-2-carboxylate.
1.38 g of the product of Step B, 2.736 g of syn isomer of cis, racemic 4-mercaptomethyl-3-�2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-2-oxo-1-azetidine �prepared by the process described in Belgian Patent No. 894,795! and 12 ml of dimethylformamide were mixed together and after 10 minutes of contact, 458 mg of lithium carbonate were added followed by stirring for 2 hours 50 mintes. The reaction mixture was poured into 100 ml of water and 60 ml of ethyl acetate and extraction was done with ethyl acetate. The organic phase was washed with water, dried and concentrated to dryness under reduced pressure. The residue was taken up in ether to obtain 3.058 g of 1,1-dimethylethyl 7-�2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-2-hydroxy-3-methoxymethyl-4-thia-1-azabicyclo�4,2,0!octane-2-carboxylate.
Analysis: C.sub.38 H.sub.41 O.sub.7 N.sub.5 S.sub.2 : molecular weight=743,91 Calculated % C 61.35 % H 5.56 % N 9.41 % S 8.62 Found: 61.1 5.7 8.9 8.4
STEP D: 1,1-dimethylethyl 7-�2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-3-methoxymethyl-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylate
4.44 g of diphosphorus tetraiodide were suspended in 35 ml of pyridine, and after stirring for 5 minutes, 3.058 g of 1,1-dimethylethyl 7-�2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-2-hydroxy-3-methoxymethyl-4-thia-1-azabicyclo�4,2,0!octane-2-carboxylate were added all at once with stirring for 2 hours 40 minutes. The pyridine was distilled off and the residue was taken up in 50 ml of ethyl acetate. After filtering, 50 ml of N hydrochloric acid were added to the filtrate with vigorous stirring and the decanted organic phase was washed with water, dried and concentrated to dryness under reduced pressure. The residue was chromatographed over silica and eluted with a mixture of methylene chloride and ethyl acetate (85-15). The fractions of interest were concentrated to dryness and crystallized from methanol to obtain 703 mg of 1,1-dimethylethyl 7-�2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-3-methoxymethyl-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylate
Analysis: C.sub.38 H.sub.39 O.sub.6 N.sub.5 S.sub.2 : molecular weight=725.89 Calculated: % C 62.88 % H 5.41 % N 9.65 % S 8.83 Found: 62.7 5.4 9.6 8.8
STEP E: Syn isomer of cis, racemic 7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-4-thia-3-methoxymethyl-1-azabicyclo �4,2,0!oct-2-en-2-carboxylic acid
246 mg of the product of Step D were dissolved in 1 ml of trifluoroacetic acid and the mixture was stirred for 50 minutes at ambient temperature. 12 ml of isopropyl ether were added and the precipiate formed was filtered off to obtain 176 mg of crude trifluoroacetate which was dissolved in ethanol. 2 drops of pyridine were added and crystallization was allowed for 1 hour to obtain 88 mg of syn isomer of cis, racemic 7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-4-thia-3-methoxymethyl-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic acid
Analysis: C.sub.15 H.sub.17 O.sub.6 N.sub.5 S.sub.2 : molecular weight=427.46 Calculated % C 42.15 % H 4.01 % N 16.38 % S 15.00 Found: 42.2 4.0 16.2 15.0
REFERENCE EXAMPLE B
Syn isomer of cis, racemic 7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-3-�(1-methyl-1H-tetrazol-5-yl) thiomethyl!-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic acid
STEP A: 2-�(1,1-dimethylethyl)dimethylsilyloxy!-ethanol
At 20.degree. C. and under nitrogen: 18 g of tertbutyl-methylsilyl, 150 ml of dichloromethane, 175 ml of dimethylformamide and 33.6 ml of ethylene glycol were mixed together and after solution has complete, 20.1 ml of triethylamine were added over 5 minutes. Then, 1.8 g of 4-dimethylamino-pyridine were added. After 2 hours 45 minutes of stirring, the solution was poured into 120 ml of water and neutralized with N hydrochloric acid (about 40 ml) to obtain a pH of 3. After decanting, the aqueous phase was extracted with 20 ml of pentane and the combined organic phase was washed with 60 ml of water, which was extracted with 20 ml of pentane. The organic phase was dried and evaporated to dryness under reduced pressure to obtain 13.9 g of 2-�(1,1-dimethylethyl)dimethylsilyloxy!-ethanol with a boiling point of 82.degree.-86.degree. C. at 16 mm/Hg.
STEP B: 2-�(1,1-dimethylethyl)dimethylsilyloxy!-acetaldehyde
Under nitrogen and with stirring, 4.71 ml of oxalyl chloride were dissolved in 120 ml of dichloromethane and the solution was cooled to -70.degree. C. Over 12 minutes while maintaining the temperature at -65.degree. C., a solution of 8 ml of dimethylsulfoxide and 26 ml of dichloromethane was introduced. Then, after 10 minutes of contact at this temperature, a solution of 8.81 g of the product of Step A, 50 ml of dichloromethane and 8.86 ml of pyridine was added over 12 minutes at -65.degree. C. After 15 minutes of contact at this temperature, 35 ml of triethylamine were added over 8 minutes at -65.degree. C. At +13.degree. C., the pH was adjusted to 4 by adding N hydrochloric acid. After decanting, re-extracting with 50 ml of dichloromethane, drying the organic phase and distilling under reduced pressure, the crude product obtained was chromatographed over silica and eluted with dichloromethane to obtain 7.95 g of 2-�(1,1-dimethylethyl)dimethylsilyloxy!-acetaldehyde.
STEP C: 1,1-dimethylethyl 2-chloro-3-(tertbutyldimethylsilyloxymethyl)oxirane-carboxylate
Using the procedure of Step B of reference Example A, while taking the precaution of introducing at the same time the solutions of potassium tertbutylate and 7.95 g of aldehyde of Step B at -20.degree. C. into a solution of 1,1-dimethylethyl dichloroacetate, and, after chromatography over silica (eluent:hexane-dichloromethane 6-4), 9.4 g of 1,1-dimethylethyl 2-chloro-3-(tertbutyldimethylsilyloxymethyl)oxirane-carboxylate.
STEP D: 1,1-dimethylethyl 7-�2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-2-hydroxy-3-�(1,1-dimethylethyl)-dimethylsilyloxymethyl!-4-thia-1-azabicyclo�4,2,0!octane-2-carboxylate
Using the procedure of Step C of reference Example A with a reaction time of 16 hours and after chromatography over silica and elution with dichloromethane and ethyl acetate (75-25), 8.31 g of syn isomer of cis 4-mercaptomethyl-3-�2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-2-oxo-1-azetidine, and product of Step C were reacted to obtain 9.09 g of 1,1-dimethylethyl 7-�2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-2-hydroxy-3-�(1,1-dimethylethyl)-dimethylsilyloxymethyl!-4-thia-1-azabicyclo�4,2,0!octane-2-carboxylate.
STEP E: 1,1-dimethylethyl 7-�2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-3-�(1,1-dimethylethyl)dimethylsilyloxymethyl!-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylate
Using the procedure of Step D of reference Example A, the contact was reduced to 55 minutes and the reaction mixture was poured into water, acidified with 2N hydrochloric acid to a pH of 1.6 and was extracted ethyl acetate. 9.09 g of the product of Step D yielded after chromatography 4 g of 1,1-dimethylethyl 7-�2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-3-�(1,1-dimethylethyl) dimethylsilyloxymethyl!-4-thia-1-azabicyclo�4,2,0!oct-2-ene-2-carboxylate.
UV Spectrum--in ethanol infl.: 233 nm E.sub.1.sup.1 : 364 infl.: 265 nm E.sub.1.sup.1 : 173 max.: 302 nm E.sub.1.sup.1 : 229 .epsilon.=18,900
STEP F: 1,1-dimethylethyl 7-�2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-3-hydroxymethyl-4-thia-1-azabicyclo�4,2,0!oct-2-ene-2-carboxylate
2.595 g of the silyl derivative of Step E were suspended in 30 ml of acetone and 4 ml of N hydrochloric acid and the solution cleared little by little after 3 hours of stirring. 7.7 ml of water saturated with sodium bicarbonate were added. The acetone was distilled off under reduced pressure and the residual gum was dissolved in 5.5 ml of ethyl acetate to which 43 ml of ether were added. After 3 hours 15 minutes of stirring, the crystals formed were filtered off, rinsed and dried to obtain 2.232 g of 1,1-dimethylethyl 7-�2(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-3-hydroxymethyl-4-thia-1-azabicyclo�4,2,0!oct-2-ene-2-carboxylate
STEP G: 1,1-dimethylethyl 7-�2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-3-chloromethyl-4-thia-1-azabicyclo�4,2,0!oct-2-ene-2-carboxylate
623 mg of the alcohol of Step F were dissolved in 8 ml of dichloromethane with 834 ml of tosyl chloride, and over 20 minutes, a solution of 534 mg of 4-dimethylamino-pyridine and 5 ml of dichloromethane was added. After stirring for one hour, 2.2 ml of N hydrochloric acid were added with stirring, and after decanting, the organic phase was dried and distilled under reduced pressure. The residue was chromatographed over silica and eluted with dichloromethane-ethyl acetate (9-1) to obtain 245 mg of 1,1-dimethylethyl 7-�2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-3-chloromethyl-4-thia-1-azabicyclo�4,2,0!oct-2-ene-2-carboxylate crystallizing from ether.
UV Spectrum--EtOH infl.: 224 nm E.sub.1.sup.1 : 441 .epsilon.=38,200 infl.: 264 nm E.sub.1.sup.1 : 179 infl.; 271 nm E.sub.1.sup.1 : 164 max.: 306 nm E.sub.1.sup.1 : 222 .epsilon.=19,200
STEP H: 1,1-dimethylethyl 7-�2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-3-�(1-methyl-1H-tetrazol-5-yl)-thiomethyl!-4-thia-1-azabicyclo�4,2,0!oct-2-ene-2-carboxylate
301 mg of the product of Step G and 114 mg of the sodium salt of 1-methyl-5-mercapto-1,2,3,4-tetrazole were dissolved in 3 ml of dimethylformamide and after 100 minutes of stirring, the solution was poured into 30 ml of water and was extracted with ethyl acetate. The organic phase was dried and distilled to dryness under reduced pressure. The residue was dissolved in 2 ml of ethyl acetate and ether is added to the limit of solubility. The crystals obtained were filtered off after 45 minutes, rinsed with ether and dried to obtained in two lots 283 mg of 1,1-dimethylethyl 7-�2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-3-�(1-methyl-1H-tetrazol-5-yl)-thiomethyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-ene-2-carboxylate
STEP I: 7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-3-�(1-methyl-1H-tetrazol-5-yl)-thiomethyl!-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic acid
Using the procedure of Step E of Example A with the crude product dissolved in sodium bicarbonate water and acidified to pH, then filtered after having distilled off a large part of the water, 371 mg of the product of Step H yielded 61 mg of 7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-3-�(1-methyl-1H-tetrazol-5-yl)-thiomethyl!-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic acid.
UV Spectrum
1) in EtOH max.: 302 nm E.sub.1.sup.1 : 295 .epsilon.=15,100
1) in EtOH/HCl 0.1N infl. 273 nm E.sub.1.sup.1 : 304 infl. 285 nm E.sub.1.sup.1 : 318 .epsilon.=16,300 infl. 292 nm E.sub.1.sup.1 : 312 .epsilon.=16,000 infl. 309 nm E.sub.1.sup.1 : 245 .epsilon.=12,500
The corresponding optically active products were prepared, particularly the syn isomer of (6S,7S) 1,1-dimethylethyl 7-�2-(2-tritylaminoethiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-3-hydroxymethyl-4-thia-1-azabicyclo�4,2,0!oct-2-ene-2-carboxylate. Using the procedure of reference Example A and starting with the syn isomer of cis (3S,4S) 4-mercaptomethyl-3-�2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-2-oxo-1-azetidine, described in French application No. 2,538,389. The reaction product possessed the following physicochemico characteristics: melting point of 180.degree. C.
UV Spectrum:
1) in ethanol: infl.: 222 nm E.sub.1.sup.1 =444 infl: 237 nm E.sub.1.sup.1 =352 max.: 302 nm E.sub.1.sup.1 =223 .epsilon.=15,900
2) in ethanol+HCl 0.1N infl.: 221 nm E.sub.1.sup.1 =464 infl.: 263 nm E.sub.1.sup.1 =204 infl.: 285 nm E.sub.1.sup.1 =294 max.: 293 nm E.sub.1.sup.1 =340 .epsilon.=22,000
2) in ethanol+HCl 0.1N (cont'd) infl.: 300 nm E.sub.1.sup.1 =299 infl.: 310 nm E.sub.1.sup.1 =230
REFERENCE EXAMPLE C
(6S,7S) 7-�(2-triphenylmethylaminothiazol-4-yl)-2-(Z)-methoxyimino-acetamido!-2-�(1,1-dimethylethyl)-oxycarbonyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-ene-3-yl!-methyl-triphenyl-phosphonium chloride
2.182 g of 1,1-dimethylethyl (6S,7S)-�-2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-8-oxo-3-chloromethyl-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylate, prepared as in Step G of reference Example B and 1.679 g of triphenyl phosphine were dissolved in 24 ml of tetrahydrofuran, and 14.1 g of silica were added. The tetrahydrofuran was distilled off under reduced pressure over 2 hours and the remainder was cooled, stirred for 26 hours at 20.degree. C. then chromatographed over silica (eluent, dichloromethane-methanol, 9/11) to obtain 1.89 g of (6S,7S) 7-�(2-triphenylmethylaminothiazol-4-yl)-2-(Z)-methoxyimino-acetamido!-2-�(1,1-dimethylethyl)-oxycarbonyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-ene-3-yl-methyl-triphenyl-phosphonium chloride.
REFERENCE EXAMPLE D
Trifluoromethane sulfonate of syn isomer of (6S,7S) 7-�3-�7-��(2-amino-4-thiazolyl) (methoxyimino)-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl! propen 2(E)-yl! thieno �2,3-b! pyridinium
STEP A: 1,1-dimethylethyl (6S,7S) 7-��2-(2-triphenylmethylamino-thiazol-4-yl! 2(Z) methoxyimino acetamido-3-�3-�(1,1-dimethylethyl)-dimethylsilyloxy! propen-1-yl!-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-2-carboxylate
1,89 g of 1,1-dimethylethyl 7-��2-(2-triphenylmethylamino-thiazol-4-yl! 2(Z) methoxyimino-acetamido!-3-methyl triphenyl-phosphonium-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-2-carboxylate hydrochloride, 30 ml of dichloromethane, 0.68 ml of 2�1,1-dimethylethyl dimethylsilyl oxy!-acetaldehyde and 0.53 ml of triethylamine were mixed together and stirred at +20.degree. C. for 14 hours. The solution was chromatographed over silica and eluted with a mixture of dichloromethane and ethyl acetate (9/1) to obtain 1.305 g of the expected product containing a mixture of isomer E (2/3) and Z (1/3).
NMR Spectrum (CDCl.sub.3): 0.9-0.92 ppm SitBu; 1.50-1.53 ppm CO.sub.2 O tBu; 2.95-3.11 ppm CH.sub.2 S; 4.05 ppm OCH.sub.3 ; 4.31-4.37 ppm CH.sub.2 O; 4.11 ppm H.sub.6 ; 5.4-5.5 ppm H.sub.7 ; 5.75-5.87 ppm and 6.11-6.24 ppm Z(1/3); 6.17-6.34 ppm and 6.97-7.16 ppm E(2/3); 6.50-6.56 ppm H.sub.5 thiazol syn; 7.34 ppm .0..sub.3.
STEP B: 1,1-dimethylethyl 7-��2-(2-triphenylmethylamino-thiazol-4-yl! 2(Z) methoxyimino-acetamido!-3-�3-hydroxy-propen-1(E)-yl)-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-2-carboxylate and 1,1-dimethylethyl 7-��2-(2-triphenylmethylamino-thiazol-4-yl! 2(Z) methoxyimino-acetamido!-3-�3-hydroxy-propen-1(Z)-yl)-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-2-carboxylate
1.305 g of the product of Step A were dissolved in 15 ml of acetone and 2 ml of a normal aqueous of hydrochloric acid were added. The mixture was stirred for 90 minutes. After concentrating to dryness by distilling under reduced pressure, aqueous sodium bicarbonate was added, and extraction was done with dichloromethane. The extracts were concentrated to dryness by distilling under reduced pressure and the residue was chromatographed over silica and eluted with a mixture of dichloromethane and ethyl acetate (1/1) to obtain 536 mg of isomer E and 369 mg of isomer Z of the expected product.
Isomer E:
IR Spectrum. (chloroform). 3607 cm.sup.-1 OH; 3405 cm.sup.-1 amide NH; 1684 cm.sup.-1 C.dbd.O; 1515 cm.sup.-1 amide II; 1772 cm.sup.-1 beta lactam C.dbd.O; 1595, 1544, 1527 cm.sup.-1 ; aromatic, thiazol, conjugated system; 1700 cm.sup.-1 tertbutyl ester; 1370 cm.sup.-1 CH.sub.3 ; 1154 cm.sup.-1 C--O--C; 2820 cm.sup.-1 OMe; 1049 cm.sup.-1 C.dbd.N--OR.
UV Spectrum: ethanol. Max. 231 nm E.sub.1.sup.1 =497 .epsilon.=32,200 Inflexion 258 nm E.sub.1.sup.1 =290 Inflexion 264 nm E.sub.1.sup.1 =264 Inflexion 270 nm E.sub.1.sup.1 =240 Max. 320 nm E.sub.1.sup.1 =245 .epsilon.=18,100
NMR Spectrum, (CDCl.sub.3) 1.51 ppm tBu; 3.05 ppm CH.sub.2 S; 4.02 ppm OCH.sub.3 ; 4.28 ppm CH.sub.2 OH; 5.48 ppm H.sub.7 ; 6.24-6.41 and 6.97-7.13 ppm ethylene H's, delta E J=15 Hz.; 7.29 ppm .0..sub.3 ; 6.53 ppm H.sub.5 thiazol "syn".
ISOMER Z:
IR Spectrum. (chloroform). 3605 cm.sup.-1 OH; 3405 cm.sup.-1 amide NH; 1685 cm.sup.-1 C.dbd.O; 1505 cm.sup.-1 amide II; 1773 cm.sup.-1 beta lactam C.dbd.O; 1704 cm.sup.-1 tertbutyl ester; 1368 cm.sup.-1 Me; 1154 cm.sup.-1 C--O--C; 1585, 1573, 1527, 1493 cm.sup.-1, trityl, aromatics, thiazole, conjugated system, 2820 cm.sup.-1 C.dbd.N--OMe; 1050 cm.sup.-1 C.dbd.N--OR.
UV Spectrum: ethanol. Inflexion 230 nm E.sub.1.sup.1 =411; Inflexion 260 nm E.sub.1.sup.1 =220; Inflexion 265 nm E.sub.1.sup.1 =198; Inflexion 271 nm E.sub.1.sup.1 =176; Max. 308 nm E.sub.1.sup.1 =194 .epsilon.=14,300
NMR Spectrum, (CDCl.sub.3) 1.49 ppm tBu; 3.06 ppm S--CH.sub.2 ; 4.04 ppm OMe; 4.27 ppm CH.sub.2 OH; 5.48 ppm H.sub.7 ; 5.85-5.98 and 6.21-6.34 ppm ethylene H's, delta Z J=11 Hz.; 6.56 ppm H.sub.5 thiazol "syn"; 7.29 ppm .0..sub.3.
STEP C: Trifluoromethane sulfonate of (6S, 7S) 7-�3-�7-�2-(2-triphenyl-methylamino thiazol-4-yl) 2(Z) (methoxyimino)-acetamido!-2-�1,1-dimethylethyloxycarbonyl!-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl! propen 2(E) yl!-thieno �2,2-b! pyridinium
222 mg of isomer E of Step B were dissolved in 4.8 ml of dichloromethane, and 3 ml of solution of 536 mg of thieno-pyridine in 10 ml of methylene chloride were added. The mixture was cooled to -70.degree. C. and then, dropwise 2.7 ml of a solution of trifluoromethane sulfonic anhydride (0.42 ml in 10 ml of methylene chloride) were added. The temperature was taken slowly to +20.degree. C. and the solution was concentrated to dryness by distilling under reduced pressure. Ethyl acetate was added to the residue which was then washed with water containing 0.7 ml of an N aqueous solution of hydrochloric acid, followed by decanting, washing with water and extracting with ethyl acetate. The extracts were concentrated to dryness by distilling under reduced pressure and the residue was chromatographed over silica and eluted with a mixture of dichloromethane and methanol (92/8) to obtain 236 mg of the expected compound (isomer E).
STEP C': Trifluoromethane sulfonate of (6S, 7S) 7-�3-�7-��(2-triphenylmethylaminothiazol-4-yl) 2(Z) (methoxyimino)-acetamido!-2-��1,1-dimethylethyloxy!-carbonyl!-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl! propen 2(Z) yl!-thieno �2,3-b! pyridinium
145 ml of isomer Z of Step B were dissolved in 5 ml of dichloromethane, and 120 .mu.l of thieno �2,3-b! pyridine were added. The mixture was cooled to -70.degree. C. and then, dropwise 1.76 ml of a methylene chloride solution of trifluoromethane sulfonic anhydride (0.42 ml in 10 ml of methylene chloride) were added. The temperature was taken slowly to +20.degree. C. and the solution was chromatographed over silica and eluted with a mixture of dichloromethane and methanol (92/8) to obtain 157 mg of the expected compound.
STEP D: Trifluoromethane sulfonate of (6S, 7S, .DELTA.Z) 7-�3-�7-��(2-(2-amino-4-thiazol-yl)-(methoxyimino)-acetamido!-2-carboxy-8-oxo-4thia-1-azabicyclo �4,2,0! oct-2-en-3-yl!-propen 2(E)-yl!-thieno �2,3-b! pyridinium
221 mg of isomer (E) of Step C and 2.5 ml of a 33% aqueous solution of formic acid were mixed together and heated to 65.degree. C. for 55 minutes and then cooled. The mixture was diluted with water, filtered and washed with ether. The aqueous phase was concentrated to dryness by distilling under reduced pressure and after water was added and drying, 93 mg of the expected product were obtained.
______________________________________I.R. Spectrum (nujol): ##STR1862##1660 cm.sup.-1 ;1550 and 1535 cm.sup.-1 , aromatic + amide II + thiazole + conjugatedsystem.1030 cm.sup.-1 CF.sub.3 SO.sub.3.U.V. Spectrum (ethanol):Max. 238 nm E.sub.1.sup.1 = 625; .epsilon. = 44,200Max. 307 nm E.sub.1.sup.1 = 251; .epsilon. = 17,700Inflexion 318 nm E.sub.1.sup.1 = 232;Inflexion 338 nm E.sub.1.sup.1 = 160;______________________________________
By formic hydrolysis, isomer Z or syn isomer hydrolyzed totally into isomer E (isomerization).
Preparation of the hydrochloride of (6S, 7S) 7-��(2-trifluoromethylaminothiazol-4-yl) 2(Z)-methoxy imino-acetamido!-2-�1,1-dimethylethyl-oxycarbonyl-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl!-methyltriphenyl phosphonium
2.182 g of 1,1-dimethyl ethyl (6S, 7S) 7-��2-(2-tritylamino-thiazol-4-yl) 2-(Z) methoxyimino-acetamido-3-chloromethyl-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-2-carboxylate and 1.679 g of triphenyl phosphine were dissolved in 24 ml of tetrahydrofuran and after 14.1 g of silica were added, the tetrahydrofuran was distilled for 2 hours, following by cooling and stirring for 26 hours at 20.degree. C. After chromatographing over silica and elution with a mixture of dichloromethane and methanol (90/10), 1.89 g of the product sought were obtained.
In the following examples there are described several preferred embodiments to illustrate the invention. However, it should be understood that the invention is not intended to be limited to the specific embodiments.
EXAMPLE 1
Syn isomer of trifluoromethane sulfonate of (6S,7S) 7-�3-�7-�(2-amino-4-thiazolyl)-(methoxyimino)-acetamido!-2-carboxy-8-oxo-4-thia-1-aza-bicyclo�4,2,0!oct-2-en-3-yl!propen-2(E)-yl!thieno�2,3-b!pyridinium
STEP A: 1,1-dimethylethyl (6S,7S)7-�2-(2-triphenylmethylamino-thiazol-4-yl)-2(Z)-methoxyimino-acetamido!-3-�3-�(1,1-dimethylethyl)dimethylsilyl-oxy!-propen-1-yl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylate
1.89 g of hydrochloride of 1,1-dimethylethyl 7-�2-(triphenylmethylamino-thiazol-4-yl)-2(Z)methoxyimino-acetamido!-3-�methyltriphenyl-phosphonium!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylate, 30 ml of dichloromethane, 0.68 ml of 2-(1,1-dimethylethyl-dimethylsilyl-oxy)-acetaldehyde, and 0.53 ml of triethylamine were mixed together, and stirred at +20.degree. C. for 14 hours. The solution was chromatographed over silica and eluted with a mixture of dichloromethane and ethyl acetate (9/1) to obtain 1.305 g of 1,1-dimethylethyl (6S,7S) 7-�2-(triphenylmethylamino-thiazol-4-yl)-2(Z)-methoxyimino-acetamido!-3-�3-�(1,1-dimethylethyl)dimethylsilyl-oxy!-propen-1-yl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylate containing a mixture of isomer E (2/3) and Z (1/3).
NMR Spectrum (CDCl.sub.3): 0.90-0.92 ppm SltBu 1.50-1.53 ppm CO.sub.2 tBu 2.95-3.11 ppm CH.sub.2 S 4.05 ppm OCH.sub.3 4.31-4.37 ppm CH.sub.2 O 4.11 ppm H.sub.6 5.4-5.5 ppm H.sub.7 5.75-5.87 ppm and Z(1/3) 6.11-6.24 ppm 6.17-6.34 ppm and E(2/3) 6.97-7.16 ppm 6.50-6.56 ppm H.sub.5 thiazole, syn 7.34 ppm .0..sub.3.
STEP B: 1,1-dimethylethyl 7-�2-(2-triphenylmethylamino-thiazol-4-yl)-2(Z)-methoxyimino-acetamido!-3-�3-hydroxypropen-1(E)-yl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylate and 1,1-dimethylethyl 7-�2-(2-triphenylmethylamino-thiazol-4-yl)-2(Z)-methoxyimino-acetamido-3-�3-hydroxypropen-1(Z)-yl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylate
1.305 g of the product of Step A of Example 1 were dissolved in 15 ml of acetone, 2 ml of an aqueous normal solution of hydrochloric acid were added with stirring for 150 minutes, followed by concentration to dryness by distillation under reduced pressure. After adding sodium bicarbonate water, extracting with dichloromethane, and concentrating the extracts to dryness by distilling under reduced pressure, the residue was chromatographed over silica and eluted with a mixture of dichloromethane and ethyl acetate (1/1) to obtain 536 mg of the E isomer of 1,1-dimethylethyl 7-�2(2-triphenylmethylamino-thiazol-4-yl)-2(Z)-methoxyimino-acetamido!-3-�3-hydroxypropen-1(E)-yl!-8-oxo-4-thia-1-aza-bicyclo�4,2,0!oct-2-en-2-carboxylate and 369 mg of the Z isomer of the said product.
I.R. Spectrum (chloroform): isomer E 3607 cm.sup.-1 OH 3405 cm.sup.-1 amide NM 1684 cm.sup.-1 C.dbd.O 1515 cm.sup.-1 amide II 1772 cm.sup.-1 lactam C.dbd.O 1595 cm.sup.-1 ; 1544 cm.sup.-1 ; 1527 cm.sup.-1 ; aromatic thiazole, conjugated system. 1700 cm.sup.-1 tertbutyl ester 1370 cm.sup.-1 CH.sub.3 1154 cm.sup.-1 C--O--C 2820 cm.sup.-1 OMe 1049 cm.sup.-1 C.dbd.N--OR
U.V. Spectrum (Ethanol) max. 231 nm E.sub.1.sup.1 =497 .epsilon.=32,200 infl. 258 nm E.sub.1.sup.1 =290 infl. 264 nm E.sub.1.sup.1 =264 infl. 270 nm E.sub.1.sup.1 =240 max. 320 nm E.sub.1.sup.1 =245 .epsilon.=18,100
NMR Spectrum (CDCl.sub.3) 1.51 ppm tBu 3.05 ppm CH.sub.2 S 4.02 ppm OCH.sub.3 4.28 ppm CH.sub.2 OH 5.48 ppm H.sub.7 6.24-6.41 and 6.97-7.13 ppm, H of ethylenes, E J=15 Hz 7.29 ppm .0.3 6.53 ppm H.sub.5 thiazole, syn
I.R. Spectrum (chloroform): isomer Z 3605 cm.sup.-1 OH 3405 cm.sup.-1 NH amide 1685 cm.sup.-1 C.dbd.O 1505 cm.sup.-1 amide II 1773 cm.sup.-1 .beta. lactam C.dbd.O 1704 cm.sup.-1 tertbutyl ester 1368 cm.sup.-1 Me 1154 cm.sup.-1 C--O--C 1585 cm.sup.-1, 1573 cm.sup.-1, 1527 cm.sup.-1, 1493 cm.sup.-1, trityl aromatics, thiazole, conjugated system 2820 cm.sup.-1 C.dbd.N--OMe 1050 cm.sup.-1 C.dbd.N--OR
U.V. Spectrum (ethanol) infl. 230 nm E.sub.1.sup.1 =411 infl. 260 nm E.sub.1.sup.1 =220 infl. 265 nm E.sub.1.sup.1 =198 infl. 271 nm E.sub.1.sup.1 =176 max. 308 nm E.sub.1.sup.1 =194 .epsilon.=14,300
NMR Spectrum (CDCl.sub.3) 1.49 ppm tBu 3.06 ppm S--CH.sub.2 4.04 ppm OMe 4.27 ppm CH.sub.2 OH 5.48 ppm H.sub.7 5.85 ppm-5.98 ppm and 6.21-6,34 ppm, H of ethylenes .DELTA.Z J=11 Hz 6.56 ppm H.sub.5 thiazole "syn" 7.29 ppm .0..sub.3
STEP C: (6S,7S)trifluoromethane sulfonate of 7-�3-�7-�2-(2-triphenylmethylamino-thiazol-4-yl)-2(Z)-methoxyimino-acetamido-2-�1,1-dimethylethyloxy-carbonyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!-propen-2-(E)-yl!thieno�2,3-b!pyridinium
222 mg of the E isomer of Step B were dissolved in 4.8 ml of dichloromethane, and to this was added 3 ml of a solution of 536 mg of thienopyridine and 10 ml of methylene chloride. After cooling to -70.degree. C. 2.7 ml of a solution of 0.43 ml of trifluoromethane sulfonic anhydride in 10 ml of methylene chloride were added dropwise. The temperature was slowly raised to -20.degree. C., followed by concentrating to dryness by distilling under reduced pressure. Ethyl acetate was added to the residue which was then washed with water containing 0.7 ml of a N aqueous solution of hydrochloric acid, decanted, washed with water, extracted with ethyl acetate, and the extracts were concentrated to dryness by distilling under reduced pressure. The residue was chromatographed over silica and eluted with a mixture of dichloromethane and methanol (92/8) to obtain 236 mg of isomer E of (6S,7S) trifluoromethane sulfonate of 7-3-�7-�2-(2-triphenylmethylamino-thiazol-4-yl)2(Z)-methoxyimino-acetamido!-2-�1,1-dimethylethyl-oxy-carbonyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!-propen-2(E)yl!thieno �2,3-b!pyridinium.
STEP C': (6S,7S) trifluoromethane sulfonate of 7-�3-�7-�(2-triphenylmethylamino-thiazol-4-yl)-2(Z)-methoxyimino-acetamido!-2-�1,1-dimethylethyl-oxy-carbonyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl! propen-2(Z)-yl!thieno�2,3-b!pyridinium
145 mg of the Z isomer of Step B of Example 1 were dissolved in 5 ml dichloromethane, and 120 .mu.l of thieno�2,3-b!-pyridine were added followed by cooling to -70.degree. C. 1.76 ml of a solution of 0.42 ml of trifluoromethane sulfonic anhydride in 10 ml of methylene chloride were added dropwise, then the temperature was slowly raised to +20.degree. C. The solution was chromatographed over silica and eluted with a mixture of dichloromethane and methanol (92/8) to obtain 157 mg of (6S,7S) trifluoromethane sulfonate of 7-�3-�2-�(2-triphenylmethylamino-thiazol-4-yl)-2(Z)-methoxyimino-acetamido!-2-�1,1-dimethylethyl-oxy-carbonyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!propen-2(Z)-yl!thieno!-�2,3-b!pyridinium.
STEP D: Syn isomer of (6S,7S) trifluoromethane sulfonate of 7-�3-�7-�(2-amino-4-thiazolyl)-methoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!propen-2(E)-yl!thieno�2,3-b!pyridinium
221 mg of isomer E of Step C and 2.5 ml of a 33% aqueous solution of formic acid were mixed together and heated to 65.degree. C. for 55 minutes, then cooled, diluted with water, filtered and washed with ether. The aqueous phase was concentrated to dryness by distilling under reduced pressure and water was added and after separating and drying, 93 mg of syn isomer of (6S,7S) trifluoromethane sulfonate of 7-�3-�7-�(2-amino-4-thiazolyl)-methoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!propen-2(E)-yl!thieno �2,3-b!pyridinium were obtained.
______________________________________I.R. Spectrum (nujol): ##STR1863##1660 cm.sup.-11550 and 1535 cm.sup.-1 aromatic + amide II + thiazole + conjugatedsystem.1030 cm.sup.-1 CF.sub.3 SO.sub.3U.V. Spectrum (ethanol):max. 238 nm E.sub.1.sup.1 = 625 .epsilon. = 44,200max. 307 nm E.sub.1.sup.1 = 251 .epsilon. = 17,700infl. 318 nm E.sub.1.sup.1 = 232Infl. 338 nm E.sub.1.sup.1 = 166NMR Spectrum (DMSO):3.83 ppm OCH.sub.35.55 to 6.44 ppm CH.sub.2.sup.+ 1H ethylene6.81 ppm H.sub.5 thiazole7.23 ppm NH.sub.27.84 to 9.24 ppm aromatics______________________________________
By hydrolysis with formic acid, the isomer Z hydrolyzed entirely into isomer E (isomerization).
EXAMPLE 2
Syn isomer of (6S,7S) 7-�2-(2-aminothiazol-4-yl)-2(Z)-methoxyimino-acetamido!-3-�3-(1-methyl-1H-1,2,3,4-tetrazol-5-yl)thio-propen-(E)-yl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic acid
STEP A: 1,1-dimethylethyl 7-�2-(2-triphenylmethylamino-thiazol-4-yl)-2(Z)-methoxyimino-acetamido!-3-�3-(1-methyl-1H-1,2,3,4-tetrazol-5-yl)thio-propen-(E)-yl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylate
37 ml of 1,1-dimethylethyl 7-�2-(2-triphenylamino-thiazol-4-yl)-2(Z)-methoxyimino-acetamido!-3-�3-hydroxypropen-1(E)-yl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylate, 24 mg of tetrabutyl ammonium iodide, 0.8 ml of methylene chloride and 23 .mu.l of 2,6-lutidine were mixed together and cooled to -70.degree. C. Then, dropwise, 0.25 ml of a solution of trichloromethane sulfonic anhydride, titrating 0.42 ml of anhydride per 10 ml of methylene chloride were added, followed by 14 mg of the sodium salt of 1-methyl-5-mercapto-1,2,3,4-tetrazole and then 0.5 ml of dimethylformamide. After stirring at 20.degree. C. and concentrating to dryness, the residue was chromatographed over silica and eluted with a mixture of methylene chloride and ethyl acetate (9/1) to obtain 1,1-dimethylethyl 7-�2-(2-triphenylmethylamino-thiazol-4-yl)-2(Z)-methoxyimino-acetamido!-3-�3-(1-methyl-1H-1,2,3,4-tetrazol-5-yl)thio-propen-(E)-yl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylate.
STEP B: 7-�2-(2-aminothiazol-4-yl)-2(Z)-methoxyimino-acetamido!-3-�3-(1-methyl-1H-1,2,3,4-tetrazol-5-yl)thio-propen-(E)-yl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic acid
329 mg of the compound of Step A and 9.6 ml of a 33% aqueous solution of formic acid were mixed together and heated for 25 minutes at +65.degree. C., then cooled, diluted with water, filtered, and concentrated to dryness by distilling under reduced pressure. The residue was triturated in water and the insoluble matter formed was eliminated by filtering, and after concentrating to dryness, 142 mg of 7-�2-(2-aminothiazol-4-yl)-2(Z)-methoxyimino-acetamido!-3-�3-(1-methyl-1H-1,2,3,4-tetrazol-5-yl)thio-propen-(E)-yl!-8-oxo-4-thia-1-azabicyclo �4,2,0!oct-2-en-2-carboxylic acid with a specific rotation of �.alpha.!.sub.D.sup.20 =-99.degree. (c=0.8% DMSO) were obtained.
______________________________________I.R. Spectrum (nujol):3410 cm.sup.-1 ; 3300 cm.sup.-1 ; 3210 cm.sup.-1 absorption OH/NH ##STR1864##1665 cm.sup.-1 other carbonyl;1626 cm.sup.-1 ;1556 cm.sup.-1 aromatic conjugated system NH.sub.2U.V. Spectrum (ethanol HCl, 0.1N):max. 239 nm E.sub.1.sup.1 = 390 .epsilon. = 21,000max. 266 nm E.sub.1.sup.1 = 414 .epsilon. = 22,300Infl. 280 nm E.sub.1.sup.1 = 390max. 329 nm E.sub.1.sup.1 = 304 .epsilon. = 16,300NMR Spectrum (DMSO)3.86 and 3.94 ppm NCH.sub.3 and OMe4.03-4.10 ppm CCH.sub.2 S5.56 to 5.73 ppm H.sub.7 .beta. lactam (cis) ##STR1865## ##STR1866##6.84 ppm H.sub.5 thiazole syn7.22 ppm NH.sub.29.17-9.27 ppm NHCO______________________________________
EXAMPLE 3
Internal salt of syn isomer of (6S,7S) 7-�3-�7-�2-(2-aminothiazol-4-yl)-2-(methoxyimino)-acetamido!-2-carboxy-8-oxo-4-thia-1-azabiclo�4,2,0!-oct-2-en-3-yl!propen-2-(E)-yl!thieno�2,3-b!pyridinium
281 mg of the product of Step C of Example 1 were dissolved in 3.17 ml of 66% formic acid, and the solution was heated at 65.degree. C. for two hours. It was then diluted with 3.2 ml of water and filtered and the filtrate was concentrated to dryness under reduced pressure. The residue was dissolved in 1.3 ml of a 1M aqueous solution of triethylamine carbonate and 1.3 ml of acetonitrile and chromatographed over silica (eluent:water-acetonitrile 9-1, then 85-15) to obtain 77 mg of internal salt of syn isomer of (6S,7S) 7-�3-�7-�2-(2-aminothiazol-4-yl)-2-(methoxyimino)-acetamido!-2-carboxy-8-oxo-4-thia-1-azabiclo �4,2,0!-oct-2-en-3-yl!-propen-2-(E)-yl!thieno�2,3-b!pyridinium.
NMR Spectrum (DMSO): 3.83 ppm (s): OCH.sub.3 5.49 ppm: H.sub.7 .beta.-lactam, cis 5.88-7.48 ppm: H of ethylene 6.80 ppm(s): H.sub.5 thiazole
IR Spectrum (nujol):
NH/OH .beta.-lactam C=0: 1760 cm.sup.-1, amide C=0: 1665 cm.sup.-1
NH.sub.2 def. aromatic, COO.sup.-, amide II thiazole: 1635 cm.sup.-1, 1600 cm.sup.-1 1558 cm.sup.-1, 1540 cm.sup.-1
C.dbd.N--OR: 1035 cm.sup.-1
EXAMPLE 4
Trifluoroacetate of Syn Isomer of (6S,7S) 7-�2-(2-aminothiazol-4-yl)-2-(methoxyimino)-acetamido!-3-�3-acetoxy-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic Acid
Step A: 1,1-dimethylethyl 7-�2-(2-tritylaminothiazol-4-yl)-2-(Z)-methoxyimino-acetamido!-3-�(3-acetoxy)-propen-1(E)-yl!-8-oxo-4-thia-1-azabicyclo�4,2,0! oct-2-en-2-carboxylate
300 mg of the E isomer of Example 1 Step B, 1.5 ml of pyridine and 0.73 ml of acetic anhydride were stirred for 2 hours at ambient temperature. 20 ml of water and 10 ml of N hydrochloric acid were added, followed by extraction with methylene chloride. 395 mg of crude product were obtained which was chromatographed over silica and eluted with a mixture of methylene chloride and ethyl acetate (6-4) to obtain 255 mg of 1,1-dimethylethyl 7-�2-(2-tritylaminothiazol-4-yl)2-(Z)-methoxyimino-acetamido!-3-�(3-acetoxy)-propen-1(E)-yl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylate melting at .perspectiveto.170.degree. C.
Step B: Trifluoroacetate of Syn Isomer of (6S,7S)7-/2-(2-aminothiazol-4-yl)2-methoxyimino)-acetamido!-3-�3-acetoxy-1(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic Acid
210 mg of the product of Step A and 1.05 ml of trifluoroacetic acid with 10% of water were stirred for 55 minutes at ambient temperature and 5 ml of ether were added with stirring for a further hour, then, after separating, 133 mg of trifloroacetate of syn isomer of (6S,7S) 7-�2-(2-aminothiazol-4-yl)-2-(methoxyimino)-acetamido!-3-�3-acetoxy-1(E)propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0! oct-2-en-2-carboxylic acid were obtained.
NMR Spectrum (DMSO):
6.92 ppm: H.sub.6 of the thiazole
9.27-9.37 ppm: H amido
5.63 to 5.68 ppm: H.sub.7
4.02-4.08 ppm: H.sub.5
6.22 to 6.3 and 7.09 to 6.93 ppm: H ethylenes
2.07 ppm: H of acetyl
IR Spectrum (nujol):
Absorption region OH/NH .beta.-lactam C=0: 1767 cm.sup.-1, 1740 cm.sup.-1, 1698 cm.sup.-1, 1667 cm.sup.-1, 1640 cm.sup.-1,
Strong absorptions: 1140 cm.sup.-1, 1250 cm.sup.-1
UV Spectrum:
1) EtOH
max. 236 nm E.sub.1.sup.1 =387 .epsilon.=23,100
infl. 260 E.sub.1.sup.1 =256
max. 320 nm E.sub.1.sup.1 =260 .epsilon.=15,500
2) EtOH+HCl 0.1N
max. 238 nm E.sub.1.sup.1 =291 .epsilon.=17,300
max. 266 nm E.sub.1.sup.1 =331 .epsilon.=19,700
infl. 283 nm E.sub.1.sup.1 =289
max. 324 nm E.sub.1.sup.1 =234 .epsilon.=13,900
EXAMPLE 5
Trifluoromethane Sulfonate of Syn Isomer of (6S,7) 3-�7-�2-�2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!-2(Z) Propenyl Trimethylammonium and Isomer (E) Propenyl
Step A: Trifluoromethane Sulfonate of Syn Isomer of (6S,7S) 3-�7-�2-(2-tritylamino-thiazol-4-yl)-2-methoxyimino-acetamido!-2-�(1,1-dimethylethoxy)-carbonyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!propen-2(E) yl-trimethylammonium, and the Isomer (propen-2(Z)yl)
282 mg of tert.-butyl 7-�2-(2-tritylaminothiazol-4-yl)-2-(methoxyimino)-acetamido!-3-�3-hydroxy-1(E+Z)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylate were dissolved in 3 ml of methylene chloride, then cooled to -70.degree. C. and 1.6 ml of a 1.53 mmol of trimethylamine were added. 0.094 ml of trifluoromethane sulfonic anhydride were added dropwise with stirring at -70.degree. C. for 30 minutes. 7 ml of methylene chloride and 5 ml of 0.1N hydrochloric acid were added and the mixture was allowed to warm up again. The organic phase was separated and dried, then chromatographed over silica with elution by a mixture of methylene chloride and methanol (95-5) to obtain 108 mg of isomer Z(30%), 117 mg of isomer E (33%) and 53 mg of a mixture of E and Z.
Step B: Trifluoromethane Sulfonate of Syn Isomer of 3-�7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!-2-(Z) Propenyl Trimethylammonium and the 2 (E) Propenyl Isomer
108 mg of the isomer (Z) of Step A were dissolved in 2 ml of formic acid with 66% of water and stirred for 2 hours at 66.degree. C. after which it was cooled and diluted with 2 ml of water. The reaction mixture was washed with ether, then with methylene chloride, and the aqueous phase was evaporated. The residue was taken up 3 times with 5 ml of acetonitrile and 1 ml of methanol. 5 ml of methylene chloride were added to the residue, and after stirring for 1 hour and separation, 55 mg of trifluoromethane sulfonate of syn isomer of 3-�7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!-2-(Z) propenyl trimethylammonium were obtained.
NMR Spectrum (DMSO):
3.06 ppm (s): N.sup..sym. (CH.sub.3).sub.3
3.86 ppm (s): OCH.sub.3
.perspectiveto.4.10 ppm (m): CH.sub.2 --N.sup..sym.
3.02 to 3.27 ppm: S--CH.sub.2
6.72 ppm: --CH.dbd.CH--CH.sub.2 .DELTA.Z
6.81 ppm: H.sub.5 thiazole syn
9.3 ppm: NHCO
UV Spectrum
1) EtOH
max. 231 nm E.sub.1.sup.1 =336 .epsilon.=21,200
max. 302 nm E.sub.1.sup.1 =202 .epsilon.=12,700
2) EtOH+HCl 0.1N
max. 232 nm E.sub.1.sup.1 =257 .epsilon.=16,200
max. 261 nm E.sub.1.sup.1 =250 .epsilon.=15,800
max. 284 nm E.sub.1.sup.1 =237 .epsilon.=14,900
infl. 310 nm E.sub.1.sup.1 =179
By starting from the (E) isomer obtained at Step A, and operating as above, 56 mg of the expected 2(E) propenyl isomer were obtained.
NMR Spectrum (DMSO)
3.02 ppm: N.sup..sym. (Me).sub.3
3.87 ppm (s): OMe.sub.3
4.11 ppm: CH.sub.2 --N.sup..sym.
5.61 to 5.78 ppm: H.sub.7 (cis)
6.73 ppm: H.sub.5 thiazole syn
5.96 to 6.22 ppm: H ethylene .DELTA.F
7.11-7.28 ppm
UV Spectrum
1) EtOH
max. 235 nm E.sub.1.sup.1 =381 .epsilon.=24,000
max. 325 nm E.sub.1.sup.1 =244 .epsilon.=15,400
2) EtOH+HCl 0.1N
infl. 245 nm E.sub.1.sup.1 =299
max. 263 nm E.sub.1.sup.1 =318 .epsilon.=20,100
max. 332 nm E.sub.1.sup.1 =212 .epsilon.=13,400
EXAMPLE 6
Internal Salt of Syn Isomer of (6S,7S) 3-�3-�7-�(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!-2(E) Propenyloxycarbonyl!-1-methylpyridinium
Step A: 1,1-dimethylethyl (6S,7S) 7-�2-(2-trityl-aminothiazol-4-yl)-2-(Z)-methoxyimino)-acetamido!-3-�(3-(nicotinoyloxy)-1-(E) Propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylate
1.5 g of nicotinic acid were heated to reflux in 1.8 ml of thionyl chloride for one and a half hours. After taking up in toluene and evaporating, the residue was triturated with ether, then dried to obtain 2.12 g of nicotinoyl chloride hydrochloride. 258 mg of the E isomer of Step B of Example 1 were dissolved in 1 ml of pyridine, and 93 mg (0.525 mM) of the freshly prepared nicotinoyl chloride hydrochloride were added and stirred for 2 hours under an inert atmosphere. After diluting with 10 ml of methylene chloride, washing with 1N hydrochloric acid and then with a solution of sodium bicarbonate, drying and evaporating, the residue was chromatographed over silica and eluted with a mixture of methylene chloride and acetone (9-1) to obtain 232 mg of 1,1-dimethylethyl (6S,7S) 7-�2-(2-trityl-aminothiazol-4-yl)-2-(Z)-(methoxyimino)-acetamido!-3-�(3-nicotinoyloxy)-1-(E)propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylate.
Step B: Iodide of E Isomer of (6S,7S) 3-�3-�7-�2-(2-tritylaminothiazol-4-yl)-2-(Z)-methoxyimino-acetamido!-2-(1,1-dimethylethoxycarbonyl)-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!-1-(E) Propenyloxycarbonyl-1-methyl-pyridinium
225 mg of the product of Step A were dissolved in 1 ml of dimethylsulfoxide and 0.16 ml of methyl iodide were added. The mixture was stirred for 5 hours and the dimethyl sulfoxide was evaporated under reduced pressure at 40.degree. C. The residue was chromatographed over silica (eluent:methylene chloride-methanol 92-8) to obtain 187 mg of iodide of E isomer of (6S,7S) 3-�3-�7-�2-(2-trityl-aminothiazol-4-yl)-2-(Z)-methoxyimino-acetamido!-2-(1,1-dimethylethoxycarbonyl)-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!-1-(E)-propenyloxycarbonyl-1-methyl-pyridinium.
Step C: Internal Salt of Syn Isomer of (6S,7S) 3-�3-�7-�(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo�4,2,0!-oct-2-en-3-yl!-2-(E)-propenyloxycarbonyl!-1-methyl-pyridinium
187 mg of the product of Step B were dissolved in 1 ml of trifluoroacetic acid and left at ambient temperature for 10 minutes. The product was precipitated with 10 ml of isopropyl ether and after separation, the residue was dissolved in 5 ml of hot ethanol. The mixture was concentrated to about 1 ml and redissolved by heating, after which 0.05 ml of pyridine was added. By cooling, stirring for 10 minutes, separating, washing with ethanol and then with ether, 34 mg of internal salt of syn isomer of (6S,7S) 3-�3-�7-�(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!-2-(E)-propenyloxycarbonyl!-1-methylpyridinium were obtained.
NMR Spectrum (DMSO)
3.78-4.86 ppm (s): OCH.sub.3
4.05 ppm (m): H.sub.6
4.37-4.44 ppm: N.sup.+ --CH.sub.3
5.05 ppm: --CH.sub.2 O--
5.66 ppm: H.sub.7
6.24 ppm (t,d): .dbd.CH--CH.sub.2
7.15 ppm (d): --CH.dbd.CH--CH.sub.2
6.82 ppm: H.sub.5 thiazole syn
7.23 ppm: NH.sub.2
8.06 to 9.57 ppm: H pyridine and H mobile
EXAMPLE 7
Trifluoromethane Sulfonate of (6S,7S) 1-�3-�7-�2-(2-aminothiazol-4-yl)-2-(methoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!-2(Z)-propenyl!-1,4-diazabicyclooctane Trifluoroacetate
Step A: Trifluoromethane Sulfonate of 1,1-dimethylethyl (6S,7S)7-�2-(2tritylaminothiazol-4-yl)-2-(methoxyimino-acetamido!-3-�3-(1,4diazabicyclooctane)-1-(Z)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-carboxylate
300 mg of 1,1-dimethylethyl (6S,7S) 7-�2-(2-tritylaminothiazol-4-yl)-2-(methoxyimino-acetamido!-3-hydroxy-1-(Z)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-carboxylate, 6 ml of methylene chloride and 179 mg of 1,4-diazabicyclo-octane were mixed together and then cooled to -70.degree. C. Dropwise 0.114 ml of trifluoromethane sulfonic anhydride were added over 25 minutes at this temperature. After being left for 15 minutes at -15.degree. C. with stirring, 20 ml of water and 6 ml of 0.1N hydrochloric acid were poured in. Extraction was done with methylene chloride and the extracts were dried and concentrated to dryness to obtain 350 mg of crude product which was then chromatographed over silica and eluted with a mixture of methylene chloride and methanol (9-1) to obtain 240 mg of trifluoromethane sulfonate of 1,1-dimethyl ethyl (6S,7S))7-�2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-3-�3-(4-diazabicyclooctane)-1-(Z)-propenyl!8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-carboxylate.
Step B: Trifluoromethane Sulfonate of (6S,7S)1-�3-�7-��2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0!oct-2-en-3-yl!-2-(Z)propenyl!-1,4-diazabicyclooctane Trifluoroacetate
190 mg of the product of Step A and 1 ml of trifluoroacetic acid with 10% of water were stirred for 60 minutes and precipitation was caused by adding 6 ml of ether, and after filtering and drying, 146 mg of trifluoromethane sulfonate of (6S,7S)1-�3-�7-��2-(2-aminthiazol-4-yl)2-methoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!-2-(Z)propenyl!-1,4-diazabicyclooctane trifluoroacetate melting at 190.degree. C. were obtained.
NMR Spectrum (DMSO)
6.88 ppm: H.sub.5 of thiazole
9.3-9.4 ppm: H of amido
5.58 to 5.73 ppm: H.sub.6
6.73-6.87 ppm) H ethylenes .DELTA.Z
5.86 to 6.11 ppm)
UV Spectrum
1) EtOH
max. 236 nm E.sub.1.sup.1 =236 .epsilon.=18,800
max. 303 nm E.sub.1.sup.1 =150 .epsilon.=12,000
2) EtOH+0.1N HCl
max. 233 nm E.sub.1.sup.1 =176 .epsilon.=14,000
max. 261 nm E.sub.1.sup.1 =177 .epsilon.=14,000
infl. 283 nm E.sub.1.sup.1 =164
infl. 291 nm E.sub.1.sup.1 =157
infl. 311 nm E.sub.1.sup.1 =119
EXAMPLE 8
Internal Salt of Syn Isomer of (6S,7S) 4-�3-�7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!-2-(E)-propenyl!-2-methylthiazolo�5,4-b!pyridinium
Step A: Trifluoromethane Sulfonate of Syn Isomer of (6S,7S)4-��7-�2-(2-tritylaminothiazol-4-yl)-2-(Z)-methoxyimino-acetamido!-2-�1,1-dimethylethoxycarbonyl!-8-oxo-4-thia-1-azabicyclo-�4,2,0!oct-2-en-3-yl!-2-(E) propenyl!-2-methyl-thiazolo�5,4-b!pyridinium
350 mg of the Z isomer of Step B of Example 1 in 10 ml of methylene chloride and 356 mg of methylthiazolo-pyridine were cooled to -70.degree. C. and 2.34 ml of a solution made up of 0.5 ml of trifluoromethane sulfonic anhydride in 10 ml of methylene chloride were introduced. The mixture was stirred for 5 minutes at -70.degree. C. under nitrogen and then the temperature was allowed to return to 20.degree. C. After diluting with methylene chloride, washing with water, drying and evaporating to dryness under reduced pressure, the residue obtained was chromatographed over silica (eluant:methylene chloride-acetone, 9-1 then methylene chloride-methanol 92-8) to abtain 347 mg of trifluoromethane sulfonate of syn isomer of (6S,7S) 4-��7-�2-(2-tritylaminothiazol-4-yl)-2-(Z)-methoxyimino-acetamido!-2-�1,1-dimethylethoxycarbonyl!-8-oxo-4-thia-1-azabicyclo-!4,2,0!oct-2-en-3-yl!2-(E)-propenyl!-2-methylthiazolo�5,4-b!pyridinium
Step B: Internal Salt of Syn Isomer of (6S,7S) 4-�3-�7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!-2-(E)-propenyl!-2-methylthiazolo�5,4-b!Pyridinium
Using the procedure of Example 3, 330 mg of the product of Step A were reacted and elution was done with distilled water containing 5% of acetonitrile, then 10% and finally 20%. The acetonitrile was evaporated off and the residue was taken up with 1 ml of acetone, isolated and rinsed with a minimum of acetone by centrifuging to obtain 98 mg of internal salt of syn isomer of (6S,7S) 4-�3-�7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!-2-(E) propenyl!-2-methylthiazolo�5,4,-b!pyridinium.
NMR Spectrum (DMSO):
3.84 ppm: OCH.sub.3
6.80 ppm: H.sub.5 of the thiazole
5.58 ppm: H.sub.6 .beta.-lactam, cis
5.93 and 7.41 ppm: H ethylenes, .DELTA.E
UV Spectrum
1) EtOH
max. 225 nm E.sub.1.sup.1 =598 .epsilon.=34,200
infl. 260 nm E.sub.1.sup.1 =332
infl. 295 nm E.sub.1.sup.1 =306
max. 304 nm E.sub.1.sup.1 =333 .epsilon.=19,000
infl. 320 nm E.sub.1.sup.1 =256
2) EtOH+HCl 0.1N
max. 220 nm E.sub.1.sup.1 =526 .epsilon.=30,100
max. 265 nm E.sub.1.sup.1 =413 .epsilon.=23,600
infl. 280 nm E.sub.1.sup.1 =381
infl. 289 nm E.sub.1.sup.1 =357
infl. 299 nm E.sub.1.sup.1 =316
max. 331 nm E.sub.1.sup.1 =200 .epsilon.=11,400
EXAMPLE 9
Internal Salt of Syn Isomer of (6S,7S) 1-�3-�7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!-2-(E)-propenyl!5,6,7,8-tetrahydroquinolinium
Step A: Trifluoromethane Sulfonate of Syn Isomer of (6S,7S) 1-�3-�7-�2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-2-(1,1-dimethyl ethyloxycarbonyl)-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!-2-(E)-propenyl!-5,6,7,8-tetrahydroquinolinium
Using the procedure of Step A of Example 8, 162 .mu.l of 2,3-cyclohexenopyridine were reacted to obtain 73 mg of trifluoromethane sulfonate of syn isomer of (6S,7S) 1-�3-�7-�2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-2-(1,1-dimethyl ethyloxycarbonyl)-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!-2-(E)-propenyl!5,6,7,8-tetrahydroquinolinium.
Step B: Internal Salt of Syn Isomer of (6S,7S) 1-�3-�7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!-2-(E)-propenyl!-5,6,7,8-tetrahydroquinolinium
136 mg of the product of Step A were dissolved in 1.5 ml of 66% formic acid and the operation was continued as in Example 3 to obtain 25 mg of internal salt of syn isomer of (6S,7S) 1-�3-�7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!-2-(E)-propenyl!-5,6,7,8-tetrahydroquinolinium.
NMR Spectrum (DMSO)
3.84 ppm: OCH.sub.3
5.46 ppm: H.sub.7 .beta.-lactam (cis)
6.8 ppm: H.sub.5 of the thiazole syn
7.09 ppm: H ethylene .DELTA.E
max. 232 nm E.sub.1.sup.1 =411 .epsilon.=22,800
infl. 264 nm E.sub.1.sup.1 =290
infl. 274 nm E.sub.1.sup.1 =269
infl. 282 nm E.sub.1.sup.1 =239
max. 317 nm E.sub.1.sup.1 =277 .epsilon.=15,400
EXAMPLE 10
Internal Salt of Syn Isomer of (6S,7S) 7-�3-�7-�2-(2-aminothiazol-4-yl)-2-difluoromethoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0!oct-2-en-3-yl!-2-(E) propenyl!thieno�2,3-b!pyridinium
Using the procedure of Example 5, 2.527 g of 1,1-dimethylethyl 7-�2-(2-tritylaminothiazol-4-yl)-2-(Z)-difluoromethoxyimino-acetamido!-3-(3-hydroxy-(E+Z)-propen-1-yl)-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl-2-carboxylate and 1.89 ml of thieno-�2,3-b!pyridine were reacted and after hydrolysis with formic acid, 813 mg of internal salt of syn isomer of (6S,7S)7-�3-�7-�2-(2-aminothiazol-4-yl)-2-difluoromethoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl)-2-(E) propenyl!thieno�2,3-b!pyridinium with a specific rotation of �.alpha.!.sub.D =132.5.degree..+-.2.degree. (c=1% in (1-1) mixture of H.sub.2 O--CH.sub.3 CN) were obtained.
NMR Spectrum (DMSO)
2.89 to 3.06 ppm: S--CH.sub.2
5.51 ppm: H.sub.7 .beta.-lactam (cis)
7.06 ppm: H.sub.5 of the thiazole, syn
7.48 ppm: H ethylenes, .DELTA.E
UV Spectrum (ethanol)--HCl 0.1N.
max. 240 nm E.sub.1.sup.1 =614 .epsilon.=36,400
infl. 260 nm E.sub.1.sup.1 =316
infl. 280 nm E.sub.1.sup.1 =296
infl. 300 nm E.sub.1.sup.1 =258
max. 329 nm E.sub.1.sup.1 =238 .epsilon.=14,100
EXAMPLE 11
Internal Salt of Syn Isomer of (6S,7S) 4-�3-�7-�2-(2-aminothiazol-4-yl)-2-difluoromethoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!-2-(E)-propenyl!thieno�3,2-b!pyridinium
Using the procedure of Example 5, 300 mg of 1,1-dimethylethyl 7-�2-(2-tritylaminothiazol-4-yl)-2-(Z)-difluoromethoxyimino-acetamido!-3-�3-hydroxy-(E)-propen-1-yl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl-2-carboxylate and 210 mg of thieno�3,2-b-!pyridine were reacted and after treatment with formic acid and then with trifluoroacetic acid, 117 mg of product were obtained which was taken up with 0.5 ml of acetonitrile and 0.5 ml of triethylamine carbonate. The mixture was chromatographed over silica and eluted with a mixture of acetonitrile with 5% of water, then with 10% and finally with 15% of water to obtain 43 mg of internal salt of syn isomer of (6S,7S) 4-�3-�7-�2-(2-aminothiazol-4-yl-2-difluoromethoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3yl!-2-(E)-propenyl thieno�3,2-b!pyridinium.
UV Spectrum EtOH--HCl 0.1N
max. 239 nm E.sub.1.sup.1 =569 .epsilon.=33,700
infl. 260 nm E.sub.1.sup.1 =274
max. 290 nm E.sub.1.sup.1 =260 .epsilon.=15,400
max. 327 nm E.sub.1.sup.1 =254 .epsilon.=15,100
EXAMPLE 12
Trifluoromethane Sulfonate of Syn Isomer of (6S,7S) 7-�3-�7-�2-(2-aminothiazol-4-yl)-2-propenyloxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!-2-(E)-propenyl!thieno�2,3-b!pyridinium
Using the procedure of Example 5, 160 mg of 1,1-dimethylethyl 7-�2-(2-tritylaminothiazol-4-yl)-2-(Z)-propenyloxyimino-acetamido!-3-(3-hydroxy-(E)-propenyl)-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl-2-carboxylate and 2.2 ml of a solution of thienopyridine (266 mg/5 cm.sup.3 of CH.sub.2 Cl.sub.2) were reacted and after hydrolysis with formic acid, 53 mg of trifluoromethane sulfonate of syn isomer of (6S,7S) 7-�3-�7-�2-(2-aminothiazol-4-yl)-2-propenyloxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-3-yl!-2-(E)-propenyl thieno�2,3-b!pyridinium were obtained.
NMR Spectrum (DMSO)
6.80 ppm: H.sub.5 of the thiazole
6.33 ppm H ethylene, trans
7.18 ppm
5.95 ppm: --CH.dbd.CH.sub.2
7.88 ppm: H.sub.3)
8.27 ppm: H.sub.2)
8.14 ppm: H.sub.6) bicyclic aromatic
9.08 ppm: H.sub.5)
9.22 ppm: H.sub.7)
UV Spectrum
1) EtOH
max. 239 nm E.sub.1.sup.1 =686 .epsilon.=50,600
infl. 260 nm E.sub.1.sup.1 =263
max. 306 nm E.sub.1.sup.1 =264 .epsilon.=19,500
infl. 322 nm E.sub.1.sup.1 =244
2) EtOH+HCl 0.1N
max. 240 nm E.sub.1.sup.1 =612 .epsilon.=45,200
max. 270 nm E.sub.1.sup.1 =363 .epsilon.=25,500
infl. 280 nm E.sub.1.sup.1 =333
infl. 291 nm E.sub.1.sup.1 =288
infl. 301 nm E.sub.1.sup.1 =237
max. 330 nm E.sub.1.sup.1 =218 .epsilon.=16,000
EXAMPLE 13
Syn Isomer of (6S,7S) 7-�(2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-3 �3-�(5-methyl-1,3,4-thiadiazol-2-yl)thio!-1-(E)propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic Acid
Step A: Syn Isomer of (6S,7S) 1,1-dimethylethyl 7-�(2-triphenylmethyl-aminothiazol-4-yl)-2-methoxyimino-acetamido!-3-�3-�(5-methyl-1,3,4-thiadiazol-2-yl)thio!-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-carboxylate
A mixture of 184.5 mg of the E isomer of Step B of Example 1 in 4 ml of anhydrous methylene chloride, 120 mg of tetrabutylammonium iodide and 116 .mu.l of 2,6-lutidine was cooled to -70.degree. C. and 620 .mu.l of a solution (0.609M/l) of trifluoromethane sulfonic anhydride in methylene chloride was added dropwise. After 10 minutes at -70.degree. C., the temperature was allowed to return to 20.degree. C. and the solvent was evaporated off under reduced pressure. Then there were added successively while stirring, 66.1 mg of 2-mercapto 5-methyl-1,3,4-thiadiazole, 2.5 ml of dimethylformamide and 104 mg of anhydrous potassium carbonate. The mixture was stirred for half-an-hour at 20.degree.-25.degree. C. and then poured into 10 ml of N hydrochloric acid and was extracted with ethyl acetate. The extracts were washed with a 5% aqueous solution of sodium bicarbonate, then with water, dried and evaporated to dryness under reduced pressure. The residue was chromatographed over silica and eluted with a mixture of ethyl acetate and methylene chloride (15-85) to obtain 147 mg of syn isomer of (6S,7S) 1,1-dimethylethyl 7-�(2-triphenylmethylaminothiazol-4-yl)-2-methoxyimino-acetamido!-3-�3-�(5-methyl-1,3,4-thiadiazol-2-yl)-thio!-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo �4,2,0!oct-2-en-carboxylate.
Step B: Syn Isomer of (6S,7S) 7-�(2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-3-�3-�(5-methyl-1,3,4-thiadiazol-2-yl)thio!-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic Acid
At ambient temperature, 118 mg of the product of Step A and 2.3 ml of trifluoroacetic acid were stirred for 20 minutes. 25 ml of anhydrous ether were added dropwise and the mixture was centrifuged. The residue was taken up in 5 ml of ether and then the centrifuging was repeated, with the residue again taken up with 5 ml of ether, followed by drying under reduced pressure. The product was taken up in 1.5 ml of ethanol and 100 .mu.l of a 1M/l solution of pyridine in ethanol, then centrifuged twice more, with the residue being taken up in 1 ml of ether each time. After drying, 52 mg of syn isomer of (6S,7S) 7-�(2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-3-�3-�(5-methyl-1,3,4-thiadiazol-2-yl)thio!-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo �4,2,0!oct-2-en-2-carboxylic acid were obtained.
NMR Spectrum (DMSO)
6.81 ppm: H.sub.5 of the thiazole
5.64 ppm: H.sub.7
4.01 ppm: H.sub.6
6.96 and 6.19 ppm: H ethylenes
7.23 ppm: H of amino
3.85 ppm: H of the methoxy
2.68 ppm: H of the methyl of the thiadizaole
UV Spectrum EtOH--HCl 0.1N
infl. 243 nm E.sub.1.sup.1 =430
max. 267 nm E.sub.1.sup.1 =580 .epsilon.=29,300
max. 329 nm E.sub.1.sup.1 =340 .epsilon.=18,800
IR Spectrum (nujol)
General absorption NH/OH--lactam C.dbd.O: 1759 cm.sup.31 1
others C=0: 1660 cm.sup.-1
region C.dbd.C; C.dbd.N: 1630 cm.sup.-1
amide II: 1540 cm.sup.-1
EXAMPLE 14
(6S,7S) 7-�2-(2-aminothiazol-4-yl)-2-(Z)-methoxyimino-acetamido!-3-�3-(1H-tetrazol-1-yl)-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo-�4,2,0!oct-2-en-2-carboxylic Acid and (6S,7S) 7-�2-(2-aminothiazol-4-yl)-2-(Z)-(methoxyimino-acetamido!-3-�3-(2H-tetrazol-2-yl)-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic Acid
Step A: 1,1-dimethylethyl 7-�2-(2-tritylaminothiazol-4-yl)-2-(Z) methoxyimino-acetamido!-3-�3-(1H-tetrazol-1-yl)-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylate and 1,1-dimethylethyl 7-�2-(2-tritylaminothiazol-4-yl)-2-(Z)-methoxyimino-acetamido!-3-�3-(2H-tetrazol-2-yl)-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylate
230 mg of the isomer of Step B of Example 1, 149 mg of tetrabutylammonium, and 0.143 ml of 2,6-lutidine were dissolved in 5 ml of dichloroethane. The solution was cooled to -70.degree. C., and 1.7 ml of a solution of trifluoromethyl sulfonic anhydride (0.42 ml in q.s. for 10 ml of CH.sub.2 l.sub.2) were added dropwise. The temperature was allowed to return to 20.degree. C. and the solvent was evaporated off. 44 mg of 1H-tetrazole, 131 mg of potassium carbonate and 3 ml of dimethylformamide were added and after 30 minutes of stirring, the solution was poured into water containing 1.5 ml of 2N hydrochloric acid, and was extracted with ethyl acetate. The organic phase was washed with water containing 0.2N thiosulfate in excess, then dried and concentrated to dryness. The residue was chromatographed over silica and eluted with a mixture of methylene chloride and ethyl acetate, first (75,25), then (50-50) 90 mg of the "position 2" isomer and 99 mg of the "position 1" isomer were isolated.
Step B: (6S,7S) 7-�2-(2-aminothiazol-4-yl)-2-(Z)-methoxyimino-acetamido!-3-�3-(1H-tetrazol-1-yl)-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo �4,2,0!oct-2-en-2-carboxylic Acid
The 99 mg of the "position 1" isomer were dissolved in 1.2 ml of 66% formic acid and the solution was heated to 65.degree. C. for 2 hours then cooled, diluted with 1.5 ml of water, filtered and the filtrate was rinsed with water and then with ether to obtain 49 mg of (6S,7S) 7-�2-(2-aminothiazol-4-yl)-2-(Z)-methoxyimino-acetamido!-3-�3-(1H-tetrazol-1-yl)-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic Acid.
NMR Spectrum (DMSO)
3.87 ppm: H OCH.sub.3
6.11 to 6.41 and 6.84 to 7.0 ppm: H ethylenes .DELTA.E
6.84 ppm: H.sub.5 of the thiazole, syn
5.61 to 5.76 ppm: H.sub.7 .beta.-lactam cis
UV Spectrum EtOH+HCl 0.1N
max. 238 nm E.sub.1.sup.1 =377 .epsilon.=18,500
max. 263 nm E.sub.1.sup.1 =419 .epsilon.=20,600
infl. 280 nm E.sub.1.sup.1 =356
max. 325 nm E.sub.1.sup.1 =299 .epsilon.=14,700
Step C: (6S,7S) 7-�2-(2-aminothiazol-4-yl)-2-(Z)-methoxyimino-acetamido!-3-�3-(2H-tetrazol-2-yl)-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo �4,2,0!-oct-2-en-2-carboxylic Acid
Using the procedure of Step B, 90 mg of the "position 2" isomer were reacted to obtain 31 mg of the expected product.
NMR Spectrum (DMSO)
3.88 ppm: H of OCH.sub.3
6.11 to 6.44 and 6.9-7.07 ppm: H ehtylenes .DELTA.E
6.87 ppm: H.sub.5 of the thiazole, syn
5.7 ppm: H.sub.7 .beta.lactam, cis.
UV Spectrum EtOH
max. 234 nm E.sub.1.sup.1 =470 .epsilon.=23,400
infl. 260 nm E.sub.1.sup.1 =302
max. 320 nm E.sub.1.sup.1 =303 .epsilon.=15,100
EXAMPLE 15
Syn Isomer of (6S,7S) 7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-3-�3-(2-methyl-1H-imidazol-1-yl)-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic Acid
Step A: Syn Isomer of (6S,7S) 1,1-dimethylethyl 7-�2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-3-�3-(2-methylimidazol-1-yl)-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylate
Using the procedure of Step A of Example 13, 62 mg of 2-methylimidazole were reacted to obtain 82 mg of syn isomer of (6S,7S) 1,1-dimethylethyl 7-�2-(2-tritylaminothiazol-4-yl)-2-methoxyimino-acetamido!-3-�3-(2-methylimidazol-1-yl)-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylate.
Step B. Syn Isomer of (6S,7S) 7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-3-�3-(2-methyl-1H-imidazol-1-yl)-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic Acid
80.5 mg of the product of Step A and 1 ml of 66% formic acid were heated for 3 hours at 60.degree.-65.degree. C. and then was evaporated to dryness under reduced pressure. The residue was taken up twice consecutively with 5 ml of water, then evaporated to dryness. The residue was taken up in 7 ml of ether, stirred for half-an-hour, then separated to obtain 41.5 mg of syn isomer of (6S,7S) 7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-3-�3-(2-methyl-1H-imidazol-1 yl)1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic acid
NMR Spectrum (DMSO)
3.85 ppm (s): OCH.sub.3
6.55-6.61 ppm (d-j=16): H ethylenes .DELTA.E
5.58 to 5.64 ppm (m): H.sub.7 .beta.lactam, cis
7.13 ppm: H.sub.5 of the thiazole
UV Spectrum EtOH+HCl 0.1N
infl. 217 nm
max. 238 nm .epsilon.=17,300
max. 264 nm .epsilon.=19,100
infl. 281 nm
max. 327 nm .epsilon.=13,100
EXAMPLE 16
Syn Isomer of (6S,7S) 7�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-3-�(5-methylthio-1,3,4-thiadiazol-2yl)thio)-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic Acid
Using the procedure of Example 13, 2-mercapto-5-methylthio-1,3,4-thiadiazole was reacted and eluting the chromatography with a mixture of methylene chloride and ethyl acetate (95-5), then (9-1) and after unblocking the functions and purification, 69 mg of syn isomer of (6S,7S) 7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-3-�(5-methylthio 1,3,4-thiadiazol-2-yl)thio)-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic acid were obtained.
NMR Spectrum (DMSO)
6.81 ppm: H.sub.5 of the thiazole, syn
5.85 ppm: OCH.sub.3
5.64 ppm: H.sub.7 .beta.-lactam, cis
6.18 and 6.98 ppm: H of ethylenes, trans
2.74 ppm: S--CH.sub.3
UV Spectrum
1) EtOH+(1 ml DMSO)
max. 298 nm E.sub.1.sup.1 =378 .epsilon.=22,100
infl. 320 nm E.sub.1.sup.1 =350 .epsilon.=20,500
2) EtOH-HCl 0.1N
max. 280 nm E.sub.1.sup.1 =469 .epsilon.=27,500
max. 330 nm E.sub.1.sup.1 =310 .epsilon.=18,200
EXAMPLE 17
Syn Isomer (6S,7S) 7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-3-�3-(5-amino-1,3,4-thiadiazol-2-yl)thio)-�1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic Acid
Using the procedure of Example 13, 184.5 mg of the E isomer of Step B of Example 1, and 66.6 mg of 2-amino-5-mercapto-1,3,4-thiadiazole in dimethylformamide were reacted. The chromatography over silica was eluted with a mixture of methylene chloride and ethyl acetate (1-1) and the blocked functions were freed by trifluoroacetic acid to obtain 60.5 mg of syn isomer of (6S,7S) 7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-3-�3-(5-amino-1,3,4-thiadiazol-2-yl)-thio)-�1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic acid.
NMR Spectrum (DMSO)
6.82 ppm: H.sub.5 of the thiazole
3.86 ppm: OCH.sub.3
5.64 ppm: H.sub.7
6.90 ppm (d=J=1.5))
6.15 ppm (d+J=7.5 and 15)) H ethylenes E
UV Spectrum
1) EtOH
max. 287 nm E.sub.1.sup.1 =411 .epsilon.=22,800
infl. 282 nm E.sub.1.sup.1 =309
max. 322 nm E.sub.1.sup.1 =312 .epsilon.=17,300
2) EtOH-HCl 0.1N
max. 271 nm E.sub.1.sup.1 =472 .epsilon.=26,200
max. 330 nm E.sub.1.sup.1 =285 .epsilon.=15,800
EXAMPLE 18
Syn Isomer of (6S,7S) 7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-3-�3-�(9H-purin-6-yl)thio!-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic Acid
Using the procedure of Example 13, 76 mg of 6-mercaptopurine were reacted and the product was chromatographed on silica, Elution first with a mixture of methylene chloride and ethyl acetate (75-25), then with ethyl acetate alone and finally with a mixture of methylene chloride and methanol (95-5) after unblocking and the purification yielded 76 mg of syn isomer of (6S,7S) 7-�2-(2-aminothiazol-4-yl)-2-methoxyiminoacetamido!-3-�3-�(9H-purin-6-yl)thio -1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic acid
NMR Spectrum (DMSO) 6.82 ppm(s): H.sub.5 of the thiazole 5.64 ppm: H.sub.7 .beta.-lactam, cis 6.26 ppm: H ethylenes .DELTA.E 7.06 ppm:
UV Spectrum
1) EtOH+2 cm.sup.3 DMSO max. 240 nm E.sub.1.sup.1 =401 .epsilon.=23,000 max. 292 nm E.sub.1.sup.1 =423 .epsilon.=24,300 max. 320 nm E.sub.1.sup.1 =311 .epsilon.=17,800 infl. 257.410 nm
2) EtOH--HCl 0.1N infl. 240 nm E.sub.1.sup.1 =319 infl. 264 nm E.sub.1.sup.1 =375 max. 287 nm E.sub.1.sup.1 =475 .epsilon.=27,200 max. 323 nm E.sub.1.sup.1 =286 .epsilon.=16,400
EXAMPLE 19
Syn isomer of (6S,7S) 7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-3-�3-(1,3,4-thiadiazol-2-yl)thio!-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic acid
Using the procedure of Example 13, 59.1 mg of 5-mercapto-1,3,4-thiadiazole were reacted to obtain 47.1 mg of the expected product.
NMR Spectrum (DMSO) 6.85 ppm(s): H.sub.5 of the thiazole 3.87 ppm(s): OCH.sub.3 3.65 ppm: .beta.-lactam,cis 6.01 ppm (d-J=15.5) H, ethylenes, E 7.06 ppm (d-J=15.5 and 7)
UV Spectrum EtOH--HCl 0.1N infl. 241 nm E.sub.1.sup.1 =335 max. 269 nm E.sub.1.sup.1 =425 .epsilon.=22,900 max. 329 nm E.sub.1.sup.1 =278 .epsilon.=15,000
EXAMPLE 20
Syn isomer of (6S,7S) 7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!3-�3�(1,2,3-triazol-5-yl)thio!-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic acid
Using the procedure of Example 13, sodium thiolate was reacted without addition of potassium carbonate and the chromatography was done by elution with a mixture of methylene chloride and ethyl acetate (75-25). The deblocking of the functions was done with formic acid: 2 ml of 66% for 149 mg of blocked product. Stirring was maintained for 3 hours at 60.degree.-65.degree. C. and the formic acid was expelled at 30.degree. C. under reduced pressure. The residue was taken up twice in water and evaporating off each time. The residue was triturated wit ether, then separated to obtain 89 mg of product which was dissolved in 6 ml of tetrahydrofuran and 1 ml of methanol. This solution was introduced dropwise into 100 ml of ether under vigorous stirring and then after separation, 69.5 mg of syn isomer of (6S,7S)-7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-3-�3-�(1,2,3-triazol-5-yl)-thio!-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic acid were obtained.
NMR Spectrum (DMSO) 6.81 ppm(s): H.sub.5 of the thiazole, syn 3.85 ppm(s): OCH.sub.3 5.63 ppm: H.sub.7 .beta.-lactam, cis 6.76
______________________________________NMR Spectrum (DMSO)6.81 ppm (s) H.sub.5 of the thiazole, syn3.85 ppm (s) OCH.sub.35.63 ppm H.sub.7 .beta.-lactam, cis 6.76 ppm H ethylenes .DELTA.E6.08 ppmUV Spectrum EtOH - HCl 0.1 Nmax. 240 nm E.sup.1.sub.1 = 396 .epsilon. = 20,700max. 266 nm E.sup.1.sub.1 = 416 .epsilon. = 21,700infl. 282 nm E.sup.1.sub.1 = 387max. 328 nm E.sup.1.sub.1 = 320 .epsilon. = 16,700______________________________________
6.08 ppm
UV Spectrum EtOH--HCl 0.1N max. 240 nm E.sub.1.sup.1 =396 .epsilon.=20,700 max. 266 nm E.sub.1.sup.1 =416 .epsilon.=21,700 infl. 282 nm E.sub.1.sup.1 =387 max. 328 nm E.sub.1.sup.1 =320 .epsilon.=16,700
EXAMPLE 21
Syn isomer of (6S,7S) 7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-3-�3-�(4-methyl-5-trifluoromethyl-4H-1,2,4-triazol-3-yl)-thio-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic acid
Using the procedure of Example 13, 90 mg of 4-methyl-5-trifluoromethyl-4H-1,2,4-triazol-3-thione were reacted and chromatography was done by eluting with a mixture of methylene chloride and ethyl acetate (75-25). After treatment with 66% formic acid, 78 mg of syn isomer of (6S,7S) 7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-3-�3-�(4-methyl-5-trifluoromethyl-4H-1,2,4-triazol-3-yl)-thio-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic acid were obtained.
NMR Spectrum (DMSO) 3.67 and 3.85 ppm: N--CH.sub.3 and O--CH.sub.3 5.64 ppm: H.sub.7 .beta.-lactam, cis 6.2 and 6.89 ppm: H ethylenes, .DELTA.E 6.81 ppm: H.sub.5 1 of the triazole
UV Spectrum EtOH--HCl 0.1N infl. 240 nm E.sub.1.sup.1 =328 max. 260 nm E.sub.1.sup.1 =345 .epsilon.=20,900 infl. 280 nm E.sub.1.sup.1 =303 max. 326 nm E.sub.1.sup.1 =215 .epsilon.=13,000
EXAMPLE 22
Syn isomer of (6S,7S) 7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-3-�3-(thiazolo�5,4-b!pyridin-2-yl)-thio-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic acid
Using the procedure of Example 13, 205 mg of 2-mercaptothiazolo �5,4-b!pyridine were reacted and chromatographed and eluted with a mixture of methylene chloride and acetone (9-1). The functions were unblocked by formic acid on 150 mg of the product obtained and 67 mg of crude product were obtained. 45 mg of the latter were chromatographed over silica and eluted with ethyl acetate, then with a mixture of acetone, ethyl acetate and water (5-4-1) to obtain 17 mg of syn isomer of (6S,7S) 7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-3-�3-thiazolo�5,4-b!pyridin-2-yl)-thio-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic acid.
NMR Spectrum (DMSO) 6.79 ppm: H.sub.5 of the triazole 3.84 ppm: OCH.sub.3 5.54 ppm: H.sub.7 .beta.-lactam 5.98 and 7.27 ppm: H ethylenes
IR Spectrum (nujol) General absorption region OH/NH C.dbd.O .beta.-lactam: 1754 cm.sup.-1 shoulder: 1660 cm.sup.-1 maximum: 1650 cm.sup.-1 region --C.dbd.C C.dbd.N: large absorption aromatic: 1580 cm.sup.-1, 1620 cm.sup.-1 NH def. amide II: 1535 cm.sup.-1 region --CH.dbd.CH--: 975 cm.sup.-1
EXAMPLE 23
Syn isomer of (6S,7S) 7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-3-�3-(1H,1,2,4-triazol-3-yl)thio-1-(E)-propenyl!-8-oxo-4-thia-1-azabicyclo�4,2,0!oct-2-en-2-carboxylic acid
Using the procedure of Example 21, 50 mg of 1H-1,2,4-triazol-3-thione were reacted to obtain 62 mg of the expected product.
NMR Spectrum (DMSO) 5.56 to 5.71 ppm: H.sub.7 .beta.-lactam 6.04 to 6.4 ppm
______________________________________NMR Spectrum (DMSO)5.56 to 5.71 ppm H.sub.7 .beta.-lactam6.04 to 6.4 ppmand H ethylenes .DELTA.E6.84-7.02 ppm6.84 ppm H.sub.5 of the triazole, syn.UV Spectrum EtOHmax. 234 nm E.sup.1.sub.1 = 481 .epsilon. = 25,100max. 320 nm E.sup.1.sub.1 = 323 .epsilon. = 16,900______________________________________
and 6.84-7.02 ppm 6.84 ppm: H.sub.5 of the triazole, syn.
UV Spectrum EtOH max. 234 nm E.sub.1.sup.1 =481 .epsilon.=25,100 max. 320 nm E.sub.1.sup.1 =323 .epsilon.=16,900
EXAMPLE 24
Internal salt of syn isomer of (6S,7S) 2-�3-�7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0!oct-2-en-3-yl!-2-(E)-propenyl!isoquinolinium
Using the procedure of Example 21, 148 mg of the E isomer of Step B of Example 1 were reacted and after adding the trifluoromethane sulfonic anhydride and distilling off the solvent, 5 ml of acetonitrile and 52 .mu.l of isoquinoline were added. After 75 minutes, the aceonitrile was driven off and the residue was dissolved in ethyl acetate, washed with water containing an excess of 0.2N sodium thiosulfate, washed with water, dried and concentrated to dryness. The residue was chromatographed over silica and eluted with a mixture of methylene chloride and methanol (92-8) to obtain 83 mg of the blocked intermediate product. After treatment with 66% formic acid, filtering and evaporating the solvent, the residue obtained was taken up in 1 ml of acetonitrile and 1 ml of a 1M solution of triethylamine, then chromatographed over silica and eluted first with a water-acetonitrile mixture (9-1) and then with a (85-15) mixture to obtain 16.76 mg of internal salt of syn isomer of (6S,7S) 2-�3-�7-�2-(2-aminothiazol-4-yl)-2-methoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0!oct-2-en-3-yl!-2-(E)-propenyl!isoquinolinium.
NMR Spectrum (DMSO) 3.83 ppm: OCH.sub.3 5.45 ppm: H.sub.7 and CH.sub.2 --N.sup.+ 6.79 ppm: H.sub.5 of the triazole 5.91-7.42 ppm: H ethylenes, .DELTA.E
UV Spectrum EtOH max. 224 nm E.sub.1.sup.1 =951 .epsilon.=52,400 infl. 232 nm E.sub.1.sup.1 =840 infl. 262 nm E.sub.1.sup.1 =296 infl. 277 nm E.sub.1.sup.1 =252 max. 289 nm E.sub.1.sup.1 =226 .epsilon.=12,400 max. 323 nm E.sub.1.sup.1 =280 .epsilon.=15,400
EXAMPLES 25 to 39
Using the procedure of the foregoing examples the products of the Tables hereafter were obtained.
__________________________________________________________________________R R.sub.1 n.sub.2 CO.sub.2 A__________________________________________________________________________ ##STR1867## ##STR1868## O CO.sub.2 H Example 25 ##STR1869## " CO.sub.2.sup..crclbar. Example 26" ##STR1870## " CO.sub.2.sup..crclbar. Example 27" ##STR1871## " CO.sub.2 H Example 28" ##STR1872## " CO.sub.2 H Example 29" ##STR1873## " CO.sub.2.sup..crclbar. Example 30 ##STR1874## ##STR1875## O CO.sub.2 H Example 31" ##STR1876## " CO.sub.2 H Example 32" ##STR1877## " CO.sub.2 H Example 33" ##STR1878## " CO.sub.2 H Example 34 ##STR1879## ##STR1880## " CO.sub.2.sup.- Example 35 ##STR1881## ##STR1882## " CO.sub.2 H Example 36 ##STR1883## ##STR1884## O CO.sub.2 H Example 37" ##STR1885## " CO.sub.2 H Example 38 ##STR1886## ##STR1887## " CO.sub.2 H Example 39__________________________________________________________________________
EXAMPLE 40
Trifluoroacetate of (6S, 7S, .DELTA.Z) 5-�3-�7-�(2-amino-4-thiazolyl)-methoxyimino)-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl!-2(E) propenyl!-2-(trifluoromethyl)-thiazolo �4,5-c! pyridinium
321 mg of 1,1-dimethylethyl 7-�(2-tritylamino-thiazol-4-yl) (methoxyimino)-acetamido!-8-oxo-3-iodopropenyl-4-thia-1-azabicyclo �4,2,0! oct-2-en-2-carboxylate and 85 mg of trifluoromethyl-thiazolo-pyridine were stirred for 90 minutes by centrifuging in 1 ml of dry dimethylsulfoxide. After distilling off as much as possible of the solvent and concentrating to dryness under pressure reduced to less than 1 mm Hg for 3 hours, the residue was chromatographed over silica and eluted with methylene chloride, then with mixtures of methylene chloride and acetone (90-10) and methylene chloride and methanol (92-8) to obtain 410 mg of the blocked iodide of the expected product.
2 ml of trifluoroacetic acid with 10% of anisole were added to the product with stirring for 20 minutes. After cooling slightly, 25 ml of isopropyl ether were added slowly with stirring for 20 minutes to obtain 137 mg of the expected product by centrifuging.
EXAMPLE 41
(6S, 7S, .DELTA.Z) 7-�(2-amino-4-thiazolyl) (methoxyimino)-acetamido!-3-�3-�1,4-dihydro-3-formylamino-4-oxo-1-pyridyl! 1(E) propenyl-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-ene-2-carboxylic acid
The procedure of Example 40 was repeated with 85 mg of oxazolapyridine to obtain 311 mg of trifluoroacetate of the expected product. 200 mg of the latter were chromatographed over silica in HPLC in a mixture of acetonitrile and water (1-1) and eluted successively with mixtures of water with 5,10 and then 15% of acetonitrile to obtain after lyophilization 48 mg of the expected product.
______________________________________NMR Spectrum, DMSO, 250 MHz, in ppm______________________________________6.81 H.sub.5 of thiazol3.85 H of OCH.sub.35.63 H.sub.7 of the cephem4.07 H.sub.6 6.90 H ethylenes6.086.25-7.28 H.sub.5 and H.sub.6 of pyridine8.71-8.30 H.sub.2 of the pyridine and H of the formyl.______________________________________
EXAMPLE 42
Iodide of (6S, 7S, .DELTA.Z) 5-�3-�7-�(2-amino-4-thiazolyl) (difluoromethoxyimino)-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl!-2(E) propenyl!-thieno �3,2-c! pyridinium, trifluoroacetate
Using the procedure of Example 40, 200 mg of 1-1-methylethyl-7-�(2-tritylamino-thiazol-4-yl) (difluoromethoxyimino)-acetamido!-8-oxo-4-thia-3-iodopropenyl-1-azabicyclo �4,2,0! oct-2-en-2-carboxylate, 38 mg of thieno �3,2-c! pyridine were reacted to obtain 44 mg of the expected product.
UV Spectrum, in EtOH: Max. 238 nm E.sub.1.sup.1 =620; .epsilon.=51,700 Inflexion 260 nm E.sub.1.sup.1 =232; Max. 319 nm E.sub.1.sup.1 =235; .epsilon.=19,600
UV Spectrum, in EtOH/HCl 0.1N: Max. 239 nm E.sub.1.sup.1 =566; .epsilon.=47,200 Inflexion 260 nm E.sub.1.sup.1 =286; Inflexion 275 nm E.sub.1.sup.1 =249; Inflexion 284 nm E.sub.1.sup.1 =226; Max. 327 nm E.sub.1.sup.1 =190; .epsilon.=15,900
EXAMPLE 43
Iodide of (6S, 7S, .DELTA.Z) 5-�3-�7-�(2-amino-thiazol-4-yl) (difluoromethoxyimino)-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl!-2(E) propenyl!-4-methyl-thieno �3,2-c! pyridinium, (trifluoroacetate
Using the procedure of Example 42, 50 mg of methyl thieno �3,2-c! pyridine, were reacted to obtain 59 mg of the expected product.
UV Spectrum, in EtOH: Inflexion 212 nm E.sub.1.sup.1 =438 .epsilon.=37,200 Max. 238 nm E.sub.1.sup.1 =666 .epsilon.=56,600 Inflexion 260 nm E.sub.1.sup.1 =233 Max. 317 nm E.sub.1.sup.1 =236 .epsilon.=20.000
UV Spectrum, in EtOH/HCl 0.1N: Max. 234 nm E.sub.1.sup.1 =619 .epsilon.=52,600 Inflexion 259 nm E.sub.1.sup.1 =290 Inflexion 266 nm E.sub.1.sup.1 =277 Inflexion 280 nm E.sub.1.sup.1 =236 Inflexion 295 nm E.sub.1.sup.1 =193 Max. 323 nm E.sub.1.sup.1 =143 .epsilon.=16,400 Inflexion 323 nm E.sub.1.sup.1 =181
EXAMPLE 44
Iodide of (6S, 7S, .DELTA.Z) 5-�3-�7-�(2-amino-thiazol-4-yl) (fluoromethoxyimino)-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl!-2(E) propenyl!-thiazolo �4,3-c! pyridinium (trifluoroacetate)
Using the procedure of Example 40, 200 mg of 1,1-dimethylethyl-7-�2-tritylamino-thiazol-4-yl!-fluoromethoxyimino-acetamido!-8-oxo-4-thia-3-iodopropenyl-1-azabicyclo �4,2,0! oct-2-en-2-carboxylate and 35 mg of thiazolo �4,5-c! pyridine were reacted to obtain 82 mg of the expected product.
UV Spectrum, in EtOH/HCl 0.1N: Max. 224 nm E.sub.1.sup.1 =647 .epsilon.=52,900 Max. 264 nm E.sub.1.sup.1 =336 .epsilon.=27,500 Max. 331 nm E.sub.1.sup.1 =190 .epsilon.=15,500
NMR Spectrum, DMSO, 250 MHz, in ppm: 6.98 H.sub.5 of ethanol 7.14 CH.dbd.CH--CH.sub.2 5.45 to 5.90 CH.sub.2 F and CH.sub.2 N.sup.+.
EXAMPLE 45
Iodide of (6S, 7S, .DELTA.Z) 5-�3-�7-�(2-amino-thiazol-4-yl) (fluoromethoxyimino)-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl!-2(E) propenyl!-4-methyl-thieno �3,2-c! pyridinium, (trifluoroacetate)
Using the procedure of Example 44, 38 mg of methyl-thieno �3,2-c! pyridine were reacted to obtain 42 mg of the expected product.
UV Spectrum, in EtOH Max. 212 nm E.sub.1.sup.1 =440 .epsilon.=36,500 Max. 238 nm E.sub.1.sup.1 =642 .epsilon.=53,300 Inflexion 260 nm E.sub.1.sup.1 =231 Max. 317 nm E.sub.1.sup.1 =217 .epsilon.=18,000
UV Spectrum, in EtOH/CHl 0.1H: Max. 239 nm E.sub.1.sup.1 =604 .epsilon.=50,200 Inflexion 257 nm E.sub.1.sup.1 =322 Inflexion 280 nm E.sub.1.sup.1 =249 Max. 324 nm E.sub.1.sup.1 =181 .epsilon.-15,000
EXAMPLE 46
Iodide of (6S, 7S, .DELTA.Z) 5-�3-�7-�(2-amino-thiazol-4-yl) (fluoromethoxyimino)-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl�-2(E) propenyl!thieno �3,2-c! pyridinium
Using the procedure of Example 44, 52 mg of thieno �3,2-c! pyridine were reacted to obtain 77 mg of the blocked iodide of the product. The 77 mg and 0.924 ml of formic acid with 66% of water were stirred at 70.degree. C. for 150 minutes. After cooling, the precipitate was separated and the filtrate was evaporated to dryness. The residue was taken up in 0.5 ml of ethanol and 1 ml of water and taken to dryness. The residue was taken up again in 5 ml of ethyl acetate and the solid product was triturated, separated and dried to obtain 47 mg of the expected product.
UV Spectrum, in EtOH Max. 238 nm E.sub.1.sup.1 =440 .epsilon.=36,500 Inflexion 260 nm E.sub.1.sup.1 =251 Max. 320 nm E.sub.1.sup.1 =220 .epsilon.=15,500
UV Spectrum, in EtOH/HCl 0.1N: Max. 240 nm E.sub.1.sup.1 =634 .epsilon.=44,600 Inflexion 260 nm E.sub.1.sup.1 =304 Max. 325 nm E.sub.1.sup.1 =192 .epsilon.=13,500
EXAMPLE 47
Internal salt of (6S, 7S, .DELTA.Z) 5-�3-�7-�(2-amino-thiazol-4-yl)-(methoxyimino)-acetamido!2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl!-2(E) propenyl!-thiazolo �4,5-c! pyridinium
Using the producedure of Example 40, thiazolo �4,5-c! pyridine was reacted to obtain 151 mg of the trifluoroacetate of the expected product which was dissolved in a (1-1) acetonitrile-water mixture and then chromatographed by HPLC over silica and eluted successively with mixtures of water with 5,10 and 20% of acetonitrile to obtain 46.5 mg of the expected product.
UV Spectrum, in EtOH Max. 225 nm E.sub.1.sup.1 =870 .epsilon.=48,500 Inflexion 260 nm E.sub.1.sup.1 =381 Max. 320 nm E.sub.1.sup.1 =305 .epsilon.=17,000
UV Spectrum, in EtOH/HCl 0.1N: Max. 225 nm E.sub.1.sup.1 =782 .epsilon.=43,600 Max. 268 nm E.sub.1.sup.1 =468 .epsilon.=26,100 Max. 330 nm E.sub.1.sup.1 =249 .epsilon.=13,900
EXAMPLE 48
Internal salt of (6S, 7S, .DELTA.Z) 5-�3-�7-�(2-amino-thiazol-4-yl) (methoxyimino)-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl!-2(E) propenyl!2-methyl 1H-imidazolo �4,5,-c! pyridinium
Using the procedure of Example 47, 2-methyl-1H-imidazolo �4,5-c! pyridine was reacted to obtain 50 mg of the expected product.
UV Spectrum, in EtOH/HCl 0.1N: Max. 213 nm E.sub.1.sup.1 =856 .epsilon.=47,400 Inflexion 242 nm E.sub.1.sup.1 =350 Max. 267 nm E.sub.1.sup.1 =454 .epsilon.=25,200 Max. 330 nm E.sub.1.sup.1 =250 .epsilon.=13,900
EXAMPLE 49
Internal salt of (6S, 7S, .DELTA.Z) 5-�3-�7-�(2-amino-thiazol-4-yl) (methoxyimino)-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl!-2(E) propenyl!-2-phenyl-oxazolo �4,5-c! pyridinium
Using the procedure of Example 47, 2-phenyl-oxazolo �4,5-c! pyridine was reacted to obtain 90 mg of the expected product.
UV Spectrum, in EtOH: Max. 239 nm E.sub.1.sup.1 =582 .epsilon.=36,000 Inflexion 270 nm E.sub.1.sup.1 =464 Inflexion 287 nm E.sub.1.sup.1 =524 Max. 293 nm E.sub.1.sup.1 =555 .epsilon.=34,300 Inflexion 304 nm E.sub.1.sup.1 =467 Inflexion 311 nm E.sub.1.sup.1 =305
UV Spectrum, in EtOH/HCl 0.1N: Max. 241 nm E.sub.1.sup.1 =508 .epsilon.=31,400 Inflexion 278 nm E.sub.1.sup.1 =616 Max. 284 nm E.sub.1.sup.1 =617 .epsilon.-38,100 Inflexion 291 nm E.sub.1.sup.1 =609 Inflexion 305 nm E.sub.1.sup.1 =403 Max. 330 nm E.sub.1.sup.1 =241 .epsilon.=14,900
EXAMPLE 50
Internal salt of the syn isomer of (6S,7S) 5-�3-�7-�(2-amino-thiazol-4-yl)-2-(methoxyimino)-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0!-oct-2-en-3-yl!-2(E) propenyl!-2-ethyl thiazolo �4,5-c! pyridinium
Using the procedure of Example 47, 2-ethylthiazolo �4,5-c! pyridine was reacted to obtain 16 mg of the expected product.
______________________________________NMR Spectrum, DMSO, 250 MHz, in ppm:______________________________________6.79 H.sub.5 of the thiazol5.47 H.sub.7 of the cephem3.96 H.sub.6 7.33 ethylene H of the propenyl5.919.88 H.sub.2 of the pyridinium8.86 H.sub.5 and H.sub.6 of the pyridinium3.33 H of the CH.sub.2 of the ethyl1.43 H of the CH.sub.3 of the ethyl______________________________________
EXAMPLE 51
Internal salt of (6S, 7S) syn isomer of 5-�3-�7-�(2-aminothiazol-4-yl) (difluoromethoxyimino)-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl!-2(E) propenyl!-thiazolo �4,5-c! pyridinium
Using the procedure of Example 47, 1,1-dimethylethyl 7-�(2-tritylamino-thiazol-4-yl) (difluoromethoxyimino)-acetamido!-8-oxo-3-iodopropenyl-4-thia-1-azabicyclo �4,2,0! oct-2-ene-2-carboxylate was reacted to obtain 183 mg of the expected product.
UV Spectrum, in EtOH: Max. 225 nm E.sub.1.sup.1 =855 .epsilon.=50,800 Inflexion 253 nm E.sub.1.sup.1 =355 Max. 320 nm E.sub.1.sup.1 =300 .epsilon.=17,800
UV Spectrum, in EtOH/HCl 0.1N: Max. 226 nm E.sub.1.sup.1 =760 .epsilon.=45,100 Max. 262 nm E.sub.1.sup.1 =400 .epsilon.=23,700 Max. 330 nm E.sub.1.sup.1 =242 .epsilon.=14,400
EXAMPLE 52
Trifluoroacetate of (6S, 7S, .DELTA.Z) 2-amino-5-�3-�7-�(2-amino-thiazol-4-yl) (difluoromethoxyimino)-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl!-2(E) propenyl!-thiazolo �4,5-c! pyridinium
Using the procedure of Example 51, 2-amino-thiazolo �4,5-c! pyridine was reacted to obtain after stirring for 15 minutes 62 mg of trifluoroacetate of the unblocked product in 0.3 ml of ethanol and 13 .mu.l of pyridine, then centrifuging 31 mg of the expected product.
UV Spectrum, in EtOH: Inflexion 233 nm E.sub.1.sup.1 =494 Max. 249 nm E.sub.1.sup.1 =782 .epsilon.=57,600 Inflexion 291 nm E.sub.1.sup.1 =195 Max. 323 nm E.sub.1.sup.1 =285 .epsilon.=21,000
UV Spectrum, in EtOH/HCl 0.1N: Max. 248 nm E.sub.1.sup.1 =812 .epsilon.=59,800 Max. 273 nm E.sub.1.sup.1 =324 Max. 329 nm E.sub.1.sup.1 =240 .epsilon.=17,700
EXAMPLE 53
Trifluoromethane sulfonate of 7-�3-�-7-(2-amino-4-thiazolyl) (fluoromethoxyimino)-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl!-2(E) propenyl!thieno �2,3-b! pyridinium (trifluoroacetate)
Under an inert atmosphere, 150 mg of 1,1-dimemthylethyl (6S, 7S, .DELTA.Z) 3-hydroxy (E) propenyl-7-�3-�7-�(2-tritylamino-4-thiazolyl!-�(2-fluoro methyloxyimino!-acetamido!-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl!-2-carboxylate, 5 ml of methylene chloride and 107 mg of thieno �2,3-b! pyridine were mixed together, and at -70.degree. C. over about 5 minutes, 1.34 ml of a 5% by volume solution of trifluoromethane sulfonic anhydride in methylene chloride were introduced with stirring at -70.degree. C. for 15 minutes. The temperature was raised to 0.degree. C. over 15 minutes, and the solution was concentrated to dryness under reduced pressure at 5.degree. C. The residue was chromatographed on silica under nitrogen pressure and eluted with a mixture of methylene chloride and methanol (90/10) to obtain 141 mg of the expected product.
Under an inert atmosphere, the 141 mg of the said product and 1.7 ml of a 66% aqueous solution of formic acid were mixed together and stirred at 66.degree. C. for 150 minutes and then cooled. The precipatate formed was eliminated by filtering and washed with water. 20 ml of ethanol were added to the filtrate which was then concentrated to dryness by distilling under reduced pressure. 1 ml of water and 1 ml of ethanol were added to the residue which was again concentrated to dryness. 5 ml of ethyl acetate were added to the residue which was then triturated and the precipitate formed was separated, washed and dried to obtain 80 mg of incompletely unblocked product. Under an inert atmosphere, the 80 mg of the said product and 320 .mu.l of trifluoroacetic acid with 10% of water were mixed together and stirred at 20.degree. C. for 20 minutes. 5 ml of ether were added slowly, and after stirring, the precipitate formed was separated, washed and dried to obtain 68 mg of the product.
UV Spectrum, (ethanol) Max. 238 nm E.sub.1.sup.1 =497 .epsilon.=41,700 Inflexion 260 nm E.sub.1.sup.1 =190 Inflexion 300 nm E.sub.1.sup.1 =191 Max. 308 nm E.sub.1.sup.1 =203 .epsilon.=17,000 Max. 323 nm E.sub.1.sup.1 =195 .epsilon.=16,400
UV Spectrum, (ethanol+HCl 0.1N): Max. 240 nm E.sub.1.sup.1 =439 .epsilon.=36,800 Inflexion 262 nm E.sub.1.sup.1 =240 Inflexion 260 nm E.sub.1.sup.1 =227 Inflexion 301 nm E.sub.1.sup.1 =176 Max. 331 nm E.sub.1.sup.1 =170 .epsilon.-14,300
EXAMPLE 54
Internal salt of (6S, 7S, .DELTA.Z) 1-�3-�7-�(2-amino-thiazol-4-yl) (methoxyimino)-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl!-2(E) propenyl!-2-(5-nitro-1H-imidazol-1-yl)-ethyl!-pyrrolidinium
Using the procedure of Step C of reference Example D, 1-�5-nitro-1H-imidazol-1-yl) ethyl!-pyrrolidine was heated to obtain 77 mg of trifluoromethylsulfonate of the blocked product. After treatment with trifluoroacetic acid with 10% of anisole, and precipitation by isopropyl ether as in Example 47, the product obtained was chromatographed by HPLC with a water-acetonitrile mixture (85-15) to obtain 19 mg of the expected product after lyophylization.
______________________________________NMR Spectrum, DMSO, 250 MHz, in ppm.______________________________________ 6.81 H.sub.5 of the thiazol 5.52 H.sub.7 of the cephemabout 3.96 H.sub.6 7.48 (m) Delta E5.73 (d, J = 16 Hz)about 2.12 H.sub.3 and H.sub.4 pyrrolidine 3.10 to 4.87 H.sub.2 and H.sub.5 pyrrolidine, H of ethyl. 8.16 and 8.69 H.sub.2 and H.sub.3 imidazol.______________________________________
EXAMPLE 55
Internal salt of (6S,7S) 7-�3-�7-�(5-amino-1,2,4-thiadiazol-3-yl) (methoxyimino)-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl!-2(E)-propenyl!-thieno �2,3-b! pyridinium
Using the orocedure of Example 53, 1,1-dimethylethyl 7-�2-(5-tritylamino-1,2,4-thiadiazol-3-yl)-2-methoxyimino)-acetamido!-2-�3-hydroxy propen (Z)-1-yl!-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-2-carboxylate (prepared like the product of Step B of reference Example D) to obtain the trifluoromethylsulfonate of the blocked product. The unblocking was done as in Example 47 and chromatographed in HPLC over lichrosorb with a mixture of water and acetonitrile (85-15) to obtain 52 mg of the expected product after lyophylization.
UV Spectrum, (ethanol+HCl 0.1N): Max. 239 nm E.sub.1.sup.1 =780 .epsilon.=43,500 Inflexion 270 nm E.sub.1.sup.1 =302 .epsilon.=16,800 Inflexion 294 and 304 nm, Max. 330 nm E.sub.1.sup.1 =249 .epsilon.=13,900
EXAMPLE 56
(6S,7S syn .DELTA.E)7-�(2-aminothiazol-4-yl) (methoxyimino-acetamido!-8-oxo-3-�3-�(1,3,4-thiadiazol-2-yl)-thio!-1-(E)-propenyl!-4-thia-1-azabicyclo �4,2,0! oct-2-en 2-carboxylate of 2,2-dimethyl-1-oxo-propoxy!-methyl
STEP A: Iodomethyl pivalate
1.55 g of potassium iodide were dissolved in 8 ml of acetone and 1.40 g of chloromethyl pivalate were added. The mixture was stirred for 45 minutes at +70.degree. C. and then for one hour at ambient temperature and filtered to obtain solution A.
STEP B: Potassium salt of 7-�(2-aminothiazol-4-yl) (methoxyimino)-acetamido!-8-oxo-3-�3-�(1,3,4-thiadiazol-2-yl)-thio-2(E)-propenyl!-4-thia-1-azabicyclo �4,2,0! oct-2-en-2-carboxylate acid
0.129 g of anhydrous potassium carbonate was stirred for one hour at ambient temperature in 5 ml of dimethylformamide and 0.500 g of the acid prepared like the product of the example described below, starting with 2-mercapto 1,3,4-thiadiazol were added and stirred for 5 minutes to obtain solution B.
STEP C: 2,2-dimethyl-1-oxo-propoxy!-methyl (6S,7S syn .DELTA.E) 7-�(2-aminothiazol-4-yl)-(methoxyimino)-acetamido�-8-oxo-3-�3-�(1,3,4-thiadiazol-2-yl) thio!-2(E)-propenyl!-4-thia-1-azabicyclo �4,2,0! oct-2-en-2-carboxylate
Solution A was introduced rapidly into solution B and stirred for 30 minutes under an inert atmosphere. The reaction mixture was poured into 70 g of water and ice and 50 ml of ethyl acetate were added. After decanting, the mixture was re-extracted and the combined organic phases were washed with a 0.2N solution of sodium thiosulfate, a solution of sodiu M bicarbonate and an aqueous solution of sodium chloride, followed by drying and evaporating to dryness. The residue was triturted in isopropyl ether, filtered, washed with a little petroleum ether (b.p. 60.degree.-80.degree. C.) and then with isopropyl ether. The dried product was chromatographed over silica and eluted with ethyl acetate to obtain 275 mg of the expected product.
UV Spectrum, in EtOH: Max. 238 nm E.sub.1.sup.1 =372 .epsilon.=24,300 Inflexion 250 nm E.sub.1.sup.1 =299 Max. 333 nm E.sub.1.sup.1 =234 .epsilon.=15,300
UV Spectrum, in HCl 0.1N: Inflexion 245 nm E.sub.1.sup.1 =317 Max. 265 nm E.sub.1.sup.1 =349 .epsilon.=22,800 Max. 335 nm E.sub.1.sup.1 =226 .epsilon.=14,800
Preparation of syn isomer of (6S, 7S) 7-�2-(2-amino-thiazol-4-yl)2-(Z)-methoxyimino-acetamido!-3-��3-1-methyl-1H-1,2,3,4-tetrazol-5-yl!-thio!propen (E) yl!-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-2-carboxylic acid
STEP A: 1,1-dimethyl ether �7-�2-(2-triphenylmethylamino-thiazol-4-yl!-2(Z) methoxyimino-acetamido!-3-��3-(1-methyl-1H-1,2,3,4-tetrazol-5-yl)thio!-propen (E) yl!-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-2-carboxylate
37 mg of 1,1-dimethylethyl 7-�2-(2-triphenylmethylamino-thiazol-4-yl!-2(Z) methoxyimino-acetamido!-3-��(3-hydroxy)-propen-1(E)-yl!-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-2-carboxylate, 24 mg of tertabutyl ammonium iodide, 0.8 ml of methylene chloride and 23 .mu.l of 2,6-lutidine were mixed together and cooled to -70.degree. C. 0.25 ml of a solution of trifluoromethane sulfonic anhydride titrating 0.42 ml of anhydride for 10 ml of methylene chloride, were added dropwise and then 14 mg of sodium salt of 1-methyl-5-mercapto-1,2,3,4-tetrazol and then 0.5 ml of dimethylformamide were added. The mixture was stirred at 20.degree. C. and after concentrating to dryness, the residue was chromatographed over silica and eluted with a mixture of methylene chloride and ethyl acetate (9/1) to obtain the expected product.
STEP B: 7-�(2-amino-thiazol-4-yl)-2(Z) methoxyimino-acetamido!-3-��3-�1-methyl-1H-�(1,2,3,4-tetrazol-5-yl)-thio!-propen-(E)-yl!-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-2-carboxylic acid
329 mg of the compound of Step A and 9.6 ml of a 33% aqueous solution of formic acid were mixed together and heated for 75 minutes at +65.degree. C. and then cooled, diluted with water. The mixture was filtered, and the filtrate was concentrated to dryness by distilling under reduced pressure. The residue was triturated in water and the insoluble matter formed was eliminated by filtering. The filtrate was concentrated to dryness to obtain 142 mg of the expected compound.
Preparation of 1,1-dimethylethyl 7-�(2-tritylamino-thiazol-4-yl)-(Z) (methoxyimino)-acetamido!-3-�3-iodopropen-1-(E)-yl!-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-2-carboxylate
1.476 g of 1,1-dimethylethyl 7-�-(2-tritylamino-thiazol-4-yl)-(Z) (methoxyimino)-acetamido!-3-�3-hydroxy-propen-1-(E)-yl!-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-2-carboxylate, 900 mg of tetrabutylammonium iodide in 25 ml of methylene chloride and 0.932 ml of lutidine were cooled to -70.degree. C. and at -65.degree. C. to -70.degree. C. and over 5 minutes, 8.52 ml of 0.5 ml of trifluoromethylsulfonic acid anhyride extended to 10 ml with methylene chloride were added with stirring for 5 minutes. At ambient temperature, 25 ml of a 0.2N aqueous solution of sodium thiosulfate were added with stirring for 5 minutes. Then, after decanting, extraction was done with methylene chloride. The organic phases were dried and concentrated to dryness. The residue was chromatographed over silica and eluted with a mixture of methylene chloride and ethyl acetate (80-20). The product was taken up in isopropyl ether and 1.215 g of the expected product were obtained.
In the same way, the 2-(fluoromethoxyimino) or 2-(difluoromethoxyimino) derivatives were obtained with the corresponding alcohols.
EXAMPLE 57
Injectable preparations were prepared comprising 500 mg of the internal salt of (6S, 7S) 7-�3-�7-�2-�(2-amino-4-thiazolyl)-2-(Z)-difluoromethoxyimino-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl-2-(E) propenyl!-thieno �2,3-b! pyridinium, or 500 mg of internal salt of (6S, 7S, .DELTA.Z) 5-�3-�7-�(2-amino-thiazol-4-yl)-(methoxyimino)-acetamido!2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl!-2(E) propenyl!-thiazolo �4,5-c!pyridinium, or 500 mg of internal salt of (6S,7S) syn isomer of 5-�3-�7-�(2-aminothiazol-4-yl) (difluoromethoxyimino)-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl!-2(E) propenyl!thiazolo �4,5-c! pyridinium or 500 mg of trifluoromethane sulfonate of 7-�3-�7-(2-amino-4-thiazolyl) (fluoromethoxyimino)-acetamido!-2-carboxy-8-oxo-4-thia-1-azabicyclo �4,2,0! oct-2-en-3-yl!-2(E) propenyl! thieno�2,3-b!pyridinium (trifluoroacetate) and sterile aqueous excipient q.s. for 5 ml.
PHARMACOLOGICAL STUDY OF THE PRODUCTS OF THE INVENTION
Activity in vitro, method of dilutions in liquid medium
A series of tubes were prepared, in each of which the same quantity of a sterile nutritive medium was distributed, together with an increasing quantity of the product under study; then each tube was inoculated with a bacterial strain. After incubation for twenty-four or forty-eight hours in an oven at 37.degree. C., the inhibition to growth was evaluated by transillumination which enabled the minium inhibiting concentration (M.I.C.) express in .mu.g/ml to be determined. The following results were obtained.
______________________________________ Prod. Ex. 3 Prod. Ex. 10STRAINS 24 H 48 H 24 H 48 H______________________________________Staphylococcus aureus SG 511 0,08 0,15 0,08 0,15Staphylococcus aureus 285 0,15 0,3 0,08 0,15Staphylococcus aureus 54146 0,15 0,15 0,15 0,3Streptococcus pyogenes A 561 .ltoreq.0,01 .ltoreq.0,01 .ltoreq.0,01 .ltoreq.0,01Streptococcus pyogenes 77 A .ltoreq.0,01 .ltoreq.0,01 .ltoreq.0,01 .ltoreq.0,01Escherichia Coli 1894 .ltoreq.0,01 .ltoreq.0,01 .ltoreq.0,01 .ltoreq.0,01Escherichia Coli 078 .ltoreq.0,01 .ltoreq.0,01 .ltoreq.0,01 .ltoreq.0,01Escherichia Coli TEM .ltoreq.0,01 .ltoreq.0,04 0,04 0,08Escherichia Coli 1507 E .ltoreq.0,01 .ltoreq.0,01 .ltoreq.0,01 .ltoreq.0,01Escherichia Coli DC0 .ltoreq.0,01 .ltoreq.0,02 0,02 0,04Escherichia Coli DC2 .ltoreq.0,01 .ltoreq.0,01 .ltoreq.0,01 .ltoreq.0,01Salmonella typhimurium MZ 11 .ltoreq.0,01 0,01 0,04 0,04Klebsiella pneumoniae 52145 0,04 0,04 0,04 0,04Klebsiella aerogenes 1522 E 0.08 0,08 0,15 0,15Enterobacter cloacae 1321 E .ltoreq.0,01 .ltoreq.0,01 0,02 0,02Proteus mirabilis A 235 0,02 0,02 0,04 0,04Proteus vulgaris A 232 0,08 0,3 0,08 0,08______________________________________ Prod. Ex. 30 Prod. Ex. 19STRAINS 24 H 48 H 24 H 48 H______________________________________Staphylococcus aureus SG 511 0,3 0,3 0,6 0,6Staphylococcus aureus 285 0,3 0,3 0,6 0,6Staphylococcus aureus 54146 0,3 0,6 0,6 1,2Streptococcus pyogenes A 561 .ltoreq.0,01 .ltoreq.0,01 .ltoreq.0,01 .ltoreq.0,01Streptococcus pyogenes 77 A .ltoreq.0,01 .ltoreq.0,01 .ltoreq.0,01 .ltoreq.0,01Escherichia Coli 1894 .ltoreq.0,01 .ltoreq.0,01 .ltoreq.0,01 .ltoreq.0,01Escherichia Coli 078 .ltoreq.0,01 .ltoreq.0,01 0,04 0,04Escherichia Coli TEM 0,02 0,02 0,15 0,15Escherichia Coli 1507 E .ltoreq.0,01 .ltoreq.0,01 .ltoreq.0,01 .ltoreq.0,01Escherichia Coli DC0 0,04 0,04 0,15 0,15Escherichia Coli DC2 .ltoreq.0,01 .ltoreq.0,01 .ltoreq.0,01 .ltoreq.0,01Salmonella typhimurium MZ 11 0,02 0,02 0,15 0,15Klebsiella pneumoniae 52145 0,02 0,02 0,3 0,3Klebsiella aerogenes 1522 E 0,04 0,04 0,3 0,3Enterobacter cloacae 1321 E .ltoreq.0,01 .ltoreq.0,01 0,04 0,08Proteus mirabilis A 235 0,02 0,04 0,08 0,08Proteus vulgaris A 232 0,02 0,04 0,04 0,04______________________________________
__________________________________________________________________________ Product Product Product Product Product Product Product Product Example Example Example Example Example Example Example ExampleSTRAINS 40 41 42 43 44 45 46 47__________________________________________________________________________STAPHYLOCOCCUS AUREUS SG511 1.200 2.500 0.150 0.080 0.300 0.150 0.150 0.150STAPHYLOCOCCUS AUREUS SG511 S 5.000 2.500 0.150 0.150 0.600 0.300 0.150 0.150STAPHYLOCOCCUS AUREUS 285 1.200 2.500 0.150 0.150 0.300 0.150 0.150 0.150STAPHYLOCOCCUS AUREUS 54146 5.000 2.500 0.300 0.150 0.600 0.300 0.150 0.300STREPTOCOCCUS PYOGENES A 561 0.020 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 0.020 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010STREPTOCOCCUS PYOGENES 77 A 0.020 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010STREPTOCOCCUS FAECIUM M 78 L >20.000 >20.000 >20.000 >20.000 >20.000 >20.000 >20.000 20.000ESCHERICHIA COLI UC 1894 0.040 0.150 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010ESCHERICHIA COLI O 78 0.150 1.200 .ltoreq.0.010 0.020 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010ESCHERICHIA COLI TEM 0.600 2.500 0.020 0.080 0.020 0.040 0.020 .ltoreq.0.010ESCHERICHIA COLI 1507 E 0.080 0.150 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010ESCHERICHIA COLI DC 0 0.600 2.500 0.040 0.080 0.020 0.040 0.020 .ltoreq.0.010ESCHERICHIA COLI DC 2 0.080 1.200 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010SALMONELLA TYPHIMURIUM MZ 11 0.150 1.200 .ltoreq.0.010 0.040 0.020 0.020 .ltoreq.0.010 .ltoreq.0.010KLEBSIELLA PNEUMONIAE 52145 0.600 5.000 0.040 0.150 0.040 0.040 0.040 .ltoreq.0.010KLEBSIELLA AEROGENES 1082 E 20.000 >20.000 0.150 1.200 5.000 2.500 0.300 2.500KLEBSIELLA AEROGENES 1522 E 0.600 2.500 0.300 0.600 0.150 0.150 0.080 0.040ENTEROBACTER CLOACAE P 99 >20.000 >20.000 2.500 2.500 5.000 5.000 2.500 5.000ENTEROBACTER CLOACAE 1321 E 0.300 1.200 0.020 0.080 0.040 0.040 0.020 .ltoreq.0.010SERRATIA RG 2532 2.500 20.000 0.300 0.300 0.150 0.300 0.150 0.080PROTEUS MIRABILIS A 235 0.300 0.600 0.020 0.040 0.040 0.080 0.020 0.020PROTEUS VULGARIS A 232 2.500 2.500 0.040 0.040 0.020 0.080 0.020 0.020PROVIDENCIA DU 48 2.500 5.000 0.600 0.300 0.600 0.150 0.300 0.300__________________________________________________________________________ Product Product Product Product Product Product Product Product Example Example Example Example Example Example Example ExampleSTRAINS 48 49 50 51 52 53 54 55__________________________________________________________________________STAPHYLOCOCCUS AUREUS SG511 0.600 0.150 0.300 0.300 0.300 0.150 0.300 0.150STAPHYLOCOCCUS AUREUS SG511 S 0.600 0.150 0.300 0.300 0.300 0.150 0.300 0.300STAPHYLOCOCCUS AUREUS 285 0.300 0.150 0.150 0.150 0.150 0.080 0.300 0.150STAPHYLOCOCCUS AUREUS 54146 1.200 0.150 0.300 0.600 0.300 0.150 0.600 0.300STREPTOCOCCUS PYOGENES A 561 .ltoreq.0.010 .ltoreq.0.010 0.020 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010STREPTOCOCCUS PYOGENES 77 A .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010STREPTOCOCCUS FAECIUM M 78 L >20.000 >20.000 >20.000 10.000 >20.000 10.000 >20.000 10.000ESCHERICHIA COLI UC 1894 0.080 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010ESCHERICHIA COLI O 78 0.080 0.150 .ltoreq.0.010 .ltoreq.0.010 0.020 .ltoreq.0.010 0.080 0.080ESCHERICHIA COLI TEM 0.300 0.600 0.020 0.040 0.040 0.020 0.300 0.080ESCHERICHIA COLI 1507 E 0.040 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 0.020ESCHERICHIA COLI DC 0 0.300 0.600 0.040 0.040 0.040 0.020 0.300 0.040ESCHERICHIA COLI DC 2 0.040 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 .ltoreq.0.010 0.020 0.040SALMONELLA TYPHIMURIUM MZ 11 0.150 0.150 .ltoreq.0.010 0.020 0.020 .ltoreq.0.010 0.080 0.040KLEBSIELLA PNEUMONIAE 52145 0.300 0.300 0.040 0.040 0.150 0.040 0.600 0.080KLEBSIELLA AEROGENES 1082 E 20.000 10.000 0.600 1.200 0.600 1.200 10.000 >20.000KLEBSIELLA AEROGENES 1522 E 1.200 1.200 0.080 0.150 0.150 0.150 0.600 0.150ENTEROBACTER CLOACAE P 99 >20.000 5.000 5.000 2.500 2.500 2.500 5.000 20.000ENTEROBACTER CLOACAE 1321 E 0.600 0.150 0.040 0.040 0.080 0.020 0.150 0.080SERRATIA RG 2532 2.500 2.500 0.300 0.300 0.300 0.040 1.200 0.300PROTEUS MIRABILIS A 235 0.300 0.300 0.040 0.040 0.040 0.020 0.300 0.080PROTEUS VULGARIS A 232 0.300 0.300 0.150 0.040 0.040 0.040 2.500 0.600PROVIDENCIA DU 48 1.200 5.000 0.600 1.200 1.200 1.200 5.000 0.300__________________________________________________________________________
Various modifications of the compounds and methods of the invention may be made without departing from the spirit or scope thereof and it is to be understood that the invention is intended to be limited only as defined in the appended claims.

Number	Date	Country	Kind
85 12218	Aug 1985	FRX
87 01456	Feb 1987	FRX

Number	Name	Date
4908359	Costerousse et al.	Mar 1990
5262411	Shirasaka et al.	Nov 1993
5385897	Teutsch et al.	Jan 1995

	Number	Date	Country
Parent	605982	Oct 1990
Parent	151698	Feb 1988

4-thia-1-aza-bicyclo�4,2,0!oct-2-ene antibiotics

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