CA2122571C

CA2122571C - Adhesion receptor antagonists

Info

Publication number: CA2122571C
Application number: CA002122571A
Authority: CA
Inventors: Peter Raddatz; Joachim Gante; Horst Juraszyk; Hanns Wurziger; Helmut Prucher; Sabine Bernotat-Danielowski; Guido Melzer
Original assignee: Merck Patent GmbH
Current assignee: Merck Patent GmbH
Priority date: 1993-05-01
Filing date: 1994-04-29
Publication date: 2005-04-12
Anticipated expiration: 2014-04-29
Also published as: NO941592L; SK281469B6; SK48494A3; CZ285761B6; AU675698B2; CN1052231C; CN1097421A; ES2134870T3; AU6064394A; CZ101994A3; ATE181735T1; HU224549B1; JP3570744B2; GR3031271T3; US5532255A; JPH072847A; CA2122571A1; DK0623615T3; RU2145961C1; PL178131B1

Abstract

Novel compounds of the formula I
(see formula I) in which R1, X and Y have the meanings given in Patent Claim 1, and their salts, inhibit the binding of fibrinogen to the fibrinogen receptor and can be used for treating thromboses, stroke, cardiac infarction, inflam-mations, arteriosclerosis, osteoporosis and tumours.

Description

Adhesion receptor antagonists The invention relates to novel compounds of the formula I

Y
I
in which X is O, S, NH or NA, Y is an aziridino, azetidino, pyrrolidino, piperidino, 1-oxa-8-azaspiro[4.5]dec-8-yl, hexahydroazepino or 4-R4-piperazino radical which is unsubstituted or substituted once by R2, which can additionally be substituted by an OZ, S2 or N(Z)2 group and/or by carbonyl oxygen, Z is in each case H, A, phenyl-CkH2k or acyl having 1-11 C atoms, R1 is a phenyl radical which is substituted once by CN, HZN-CH2-, (A) 2N-CH2-, H2N-C (=NH) -, H2N-C (=NH) -NH-, H2N-C (=NH) -NH-CH2-, HO-NH-C (=NH) - or HO-NH-C (=NH) -NH, R2 is -CmH2~"-COORS Or -CnH2n-0-C~H2~-COORS, R3 is H, A or benzyl, R4 is H, A, benzyl or -CmH2m-COOR3, A is in each case alkyl having 1-6 C atoms, k and m are in each case 0, 1, 2 or 3, n is 0, 1 or 2, and p is 1, 2 or 3, -la-and salts thereof.
Similar compounds are known from EP-A1-0 381 033.
The invention was based on the object of discovering novel compounds possessing valuable properties, in particular those compounds which can be used for preparing pharmaceuticals.
This object was achieved by the invention. It was found that the compounds of the formula I, and their solvates and salts, possess valuable pharmacological properties while being well tolerated. In particular, they inhibit the binding of fibrinogen, fibronectin and - 2 _ the von Willebrand factor to the fibrinogen receptor of blood platelets (glycoprotein IIb/IIIa), as well as the binding of these proteins. and further adhesive proteins, such as vitronectin, collagen and laminin, to the corres-poadiag receptors on the surface of various cell types.
The compaunds consequently influence cell-cell and cell-matrix interactions. They prevent the development of blood-platelet thrombi in particular, and can therefore be used foz the treatment of thromboses, stroke, cardiac infarction, inflaamiations and arteriosclerosis. Ia addition the compounds have an effect on tumour cells, by preventing them from farming metastases. Consequently, they can also be employed as anti-tumour agents.
The compounds are also suitable as anti-microbial active substances which are able to prevent infections, for example those initiated by bacteria, fungi or yeasts.
The substances can therefore preferably be gives as accompanying anti-microbial active substances, when organisms are subjected to interventions is which exogenous, for example biomater'ials, implants, catheters or pacemakers. are employed. They act as antiseptics.
The properties of the compounds can be demon-strated by methods which are described in EP-A1-0 462 960. The inhibition of the binding of fibrin to the fibrinogen receptor can be demonstrated by the method given is EP-Al-0 381 033. The inhibitory effect on blood platelet aggregation can be demonstrated in vitro by the method of Born (Nature 4832, 927-929. 1962).
The invention relates additionally to a process for preparing a compound of the given formula I, and its salts, characterized in that (a) a compound of the formula I is liberated from one of its functional derivatives by treating with a solvo-lysing or hydrogenolysing agent, or in that (b) a compound of the formula II

2~E,,~c~rl~
_ 3 --~CH2 E
II
R
O
in which E is C1, Br, I, or a reactive esterified OH group, and R1 and X have the abovementioned meanings, is reacted with as amino compound of the formula III
H-Y III
in which Y has the abovementioned meaning, or in that (c) a compound of the formula IV
R1-NH-CHZ-CH (XH) -CHI-Y IV
in which Rl, X and Y have the abovementioned meaaiags, or one of its reactive derivatives, is reacted with a reactive derivative of carbonic acid, or in that (d) is order to prepare a guaaidino compound of the formula I (Rl = phenyl radical substituted once by HiN-C(=NH)-NH), an amino compound corresponding to the formula I, which, however, contains as amino-phenyl group in place of the radical Rl. ie treated with an amidinating agent, and/or in that, in a compound of the formula I, one or both radicals Rl and/or Y is/are transformed into (an)other radicals) Rl and/or Y, and/or a ~compouad of the formula I is converted into one of its salts by treatment with an acid or a base.
The compounds of the formula I possess at least one chiral centre and can therefore occur in several anaatiomeric forms. All these forms (e. g. D and L forms), 2~~?~"~~.
and their mixtures (e.g. the DL forms), are included is the formula I.
Both is the above aad in the following, the radicals or parameters X, Y, Z, R1 to R', A, Ac, k, m, n, p and E have the meanings given in the formulae I or II, unless otherwise expressly indicated. In the case where several groups A and/or Z are present in the molecule I, II and/or III, they can be identical or different from one another.
In the above formulae, the group A has 1-6, preferably 1,2, 3 or 4, C atoms. Specifically, A prefer-ably is methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl or tart-butyl, and, additionally, also pentyl, 1-, 2- or 3-methylbutyl, l,l-, 1,2- or 2,2-dimethylpropyl, 1-ethylpropyl, hexyl or 1-, 2-, 3- or 4-methylpentyl.
X is preferably O, or else S, NH or NA, e.g.
N_ CH3 .
Y is preferably .. 3- (R'OOC) -azetidino, 3- (R'OOC-CHs-O-) -azetidino, 2= (R'OOC-) -pyrrolidino, 3- (R'OOC-) -pyrrolidino, 2- (R'OOC-) -piperidino, 3- (R'OOC-) -piperidino, 4- (R'OOC-) -piperidino, 2- (R300C-CHz-) -piperidiao, 3- (R300C-CHs-) -piperidino, 4- (R300C-CHI-) -piperidino, 4- (R300C-CHiCHz-) -piperidino, 4-hydroxy-4- (R'OOC) -piperidino, 4-hydroxy-4- (R'OOC-CHs-) -piperidino, 4-amino-4-(R300C)-piperidiao, 4-amino-4-(R'OOC-CHs-)piperidino, 3-oxo-4-(R'OOC-CHz-)-piperidino, 2- (R300C-CH~-O-) -piperidino, 3- (R;OOC-CHz-O-) -piperidino, 4- (R;OOC-CHz-O-) -piperidino, 1-oxa-2-oxo-8-azaspiro I4 .5] -dec-8-yl, 2-, 3- or 4-(R'OOC)-hexahydroazepino, 4- (R300C-CHz-) -piperazino, 4- (R300C-CHsCHs-) -piperaziao, 2-(R300C)-piperazino, 3-(R300C)-piperaziao, or 4-benzyl-3- (R'OOC) -piperazino.
Z is preferably H, more preferably A such ae methyl or ethyl, phenyl, benzyl, acetyl or benzoyl.
Rl is preferably a phenyl radical, which is sub-stituted, as indicated, in the 4 position, or else in the 2 or 3 position, those which are specifically preferred being 2-, 3- or (in particular) 4-cyaaophenyl, 2-, 3- or ~ r- r~ ~a ~. ~ !.. ~ ., _,~
' ' - 5 _ (in particular) 4-aminomethylphenyl, 2-, 3- or (in particular) 4-dimethylaminophenyl, 2-, 3- or (in particu lar) 4-amidinophenyl, 2-, 3- or 4-guanidinophenyl or 2-, 3- or 4-guanidinomethylphenyl, 2-, 3- or (ia particular) 4-hydroxyamidinopheayl.
R' is preferably -COOR', -CHsCOOR' or -O-CHzCOOR'.
R' is preferably H, methyl, ethyl, tert-butyl or benzyl.
R' is preferably H, methyl, ethyl, benzyl or CH2COOR3.
Ac is preferably alkanoyl having 1-6 carbon atoms, such as formyl, acetyl, propionyl, butyryl, isobutyryl, valeryl or caproyl, and also benzoyl, tolyl, 1- or 2-naphthoyl or phenylacetyl.
The parameters k and m are preferably 0 or 1. The parameter n is preferably 0. The parameter p is prefer-ably 1.
Those compounds of the formula I' are preferred in which at least one of the indicated radicals, groups and/or parameters has one of the indicated preferred meanings. Some groups of preferred compounds are those of the formulae Ia to Id which correspond to the formula I
where, however, in Ia X is O;
in Ib X is O, and Rl is cyanophenyl;
in Ic X is O, and R' is aminomethylphenyl;
in Id X is O, and Rl is amidinophenyl.
Furthermore, compounds are preferred which are of the formulae Ie, as well as Iae, Ibe, Ice and Ide, which correspond to the formulae I, Ia, Ib, Ic and Id where, however in addition, Y is 3-R'-azetidino, 2-R'-pyrrolidino, 2-R'-piperidino, 3-R'-piperidino, 4-R'-piper-idino, 4-R'-piperazino or 3-R'-4-R'-piper-azino, R' is -COOR', -CH=COORS or -OCHzCOOR', and R' is -CHzCOOR'.
Smaller, selected, groups of compounds are those of the formulae If sad Ig. They correspond to the formula I where, however, in If X is O, Y is 3- (R'OOC-CHs-O-) -azetidiao, 2- (R'OOC-) -pyrrolidino, 2-, 3- or 4- (R300C-) -piperidino, 4- (R'OOC-CHz-) -piperidino, 3- or 4- (R'OOC-CHz-O-) -piperidino, 4- (R'OOC-CHI) -piperazino or 3-(R'OOC-)-4-R'- piperaziao, Rl is 4-cyanophenyl, 4-amiaomethylphenyl, 4-ami-dinophenyl. or 4-guanidinomethylphenyl, R' is H, Cl-C,-alkyl or benzyl and R' is H or benzyl, and in Ig X is 0, Y is 4- (R'OOC-) -piperidino or 4- (R'OOC-GHzO-) -piperidino, R1 is 4-cyanophenyl, 4-aminomethylphenyl or 4-amidinophenyl, and ..
R' is H, Cl-C,-alkyl or ~ beazyl .
The compounds of the formula I, and also the starting compounds for their preparation, are otherwise prepared by methods which are knows per se, as described is the literature (e.g. in the standard works, such as Houben-Weyl, Methoden der organischen Chemie (Methods of Organic Chemistry), Georg-Thieme Verlag, Stuttgart;
additionally EP-Al-0381033 and EP-Al-0462960), speeifically under reaction conditions which are knows.
and suitable, for the said reactions. In this context, use can also be made of variants which are known per se but which are not mentioned here in detail.
If desired. the starting compounds can also be formed in situ; such that they are not isolated from the reaction mixture but. instead. immediately further reacted to give the compounds of the formula I.
The compounds of the formula I can be obtained by liberating them from their functional derivatives by solvolysis. in particular hydrolysis, or by hydrogenolysis.

~~.~2~'~I
Preferred starting compounds for the solvolysis or hydrogenolysis are those which, while otherwise corresponding to the formula I, contain corresponding protected amino and/or hydroxyl groups in place of one or more free amino and/or hydroxyl groups, preferably those which carry an amino protective group in place of an H atom which is linked to an N atom. in particular those which carry an R'-N- group, where R' is an amino protec-tive group, in place of an Hr1 group, aad/or those which carry a hydroxyl protective group in place of the H atom of a hydroxyl group, e.g. those which correspond to the formula I but carry a -COOR" group, where R" is a hydroxyl protective group, in place of a -COON group.
Several - identical or different - protected amino and/or hydroxyl groups may also be present is the molecule of the starting compouund. If the protective groups which are present differ from each other, they can in many cases be eliminated selectively.
The expression "amino protective group" is well known and relates to groups which are suitable for protecting (for blocking) an amino group from chemical reactions but which are readily removable once the desired chemical reaction at another site is the molecule has been carried out. Typical groups of this nature are, in particular, vasubstituted or substituted acyl, aryl (e. g. 2,4-diaitrophenyl (DNP)); aralkoxymethyl (e. g.
beazyloxymethyl (BOM)) or aralkyl (e. g. benzyl, 4-nitro-beazyl or triphenylmethyl) groups. Since the amino protective groups are removed following the desired reaction (or sequence of reactions), their nature and size is othex~rise not critical; however, those are preferred which have 1-20, in particular 1-8, C atoms. In connection with the present process, the expression "acyl group" is to be interpreted in the widest sense. It embraces acyl groups derived from aliphatic, araliphatic, aromatic or heterocyclic carboxylic acids or sulfonic acids, such as, in particular, alkoxycarbonyl, aryloxy-carbonyl sad, above all, aralkoxycarbonyl groups.
Examples of acyl groups of this nature are alka.noyl, such 21l ~5"l.~
-~_ as acetyl, propionyl or butyryl; aralkanoyl, such as phenylacetyl; aroyl, such as benzoyl or tolyl; aryloxy-alkanoyl, such as phenoxyacetyl; alkoxycarbonyl, such as methoxycarbonyl, ethoxycarbonyl, 2,2,2,-trichloroethoxy-carbonyl, isopropoxycarbonyl, tent-butoxycarbonyl (BOC) or 2-iodoethoxycarbonyl; aralkyloxycarbonyl, such as benzyloxycarbonyl (CBZ), 4-methoxybenzyloxycarbonyl or 9-fluorenylmethoxycarbonyl (FMOC). Those amino protective groups which are preferred are BOC, DNP and BOM, and, additionally, CBZ, benzyl and acetyl.
The expression "hydroxyl protective group" is likewise well known and relates to groups which are suitable for protecting a hydroxyl group from chemical reactions but which are readily removable once the desired chemical reaction has been carried out at another site in the molecule. Typical groups of this nature are the abovementioned unsubstituted or substituted aryl, aralkyl or acyl groups, and additionally, alkyl groups.
The nature and size of the hydroxyl protective groups is not critical, since they are removed once more following the desired chemical reaction or sequence of reactions;
groups having 1-20, in particular 1-10, C atoms are preferred. Examples of hydroxyl protective groups are, inter alia, tert-butyl, benzyl, p-nitrobenzoyl, p-toluenesulfonyl and acetyl, with beazyl and acetyl being particularly preferred.
The functional derivatives of the compounds of the formula I to be used as starting compounds caa be prepared by customary methods, such as are described, for example, in the said standard works and patent applica-tions, e.g. by the reaction of compounds which correspond to the formulae II and III, with, howQVer. at least one of these compounds containing a protective group in place of a H atom. ' The liberation of the compounds of the formula I
from their functional derivatives is achieved - is dependence on the protective group used - e.g. using strong acids, expediently using trifluoroacetic acid or perchloric acid, or else using other strong inorganic ~1~«~'T~.
g -acids, such as hydrochloric acid or sulfuric acid, strong organic carboxylic acids, such as trichloroacetic acid, or sulfonic acids, such as benzenesulfonic acid or p-toluenesulfoaic acid. It is possible, but not always necessary, for as additional inert solvent to be present.
Suitable inert solvents are, preferably, organic, for example carboxylic, acids, such as acetic acid, ethers, such as tetrahydrofuran or dioxane, amides, such as dimethylformamide (DMF), halogenated hydrocarbons, such as dichloromethane, sulfoxides such as dimethyl sulfoxide (DMSO), and, is addition, alcohols, such as methanol, ethanol or isopropanol, as well as water.
Additionally mixtures of the abovementioned solvents are suitable. Trifluoroacetic acid is preferably used in excess without addition of any further solvent;
perchloric acid is used in the form of a mixture consist-ing of acetic acid sad 70% perchloric acid in the ratio 9:1. The reaction temperatures for the cleavage are expediently between about 0 and about 50°; preferably, they are between 15 and 30° (room'temperature).
The BOC group can, for example, preferably be eliminated using 40% trifluoroacetic acid in dichloro-methane, or using about 3 to 5N HC1 in dioxaae, at 15-60°, and the FMOC group using an approximately 5-20%
solution of dimethylamine, diethylamine or piperidine is DMF at 15-50°. Elimination of the DNP group is also achieved, for example, using an approximately 3-10%
solution of 2-mercaptoethanol in DMF/water at 15-30°.
Protective groups (e. g. BOM, CBZ or beazyl) which are removable by hydrogenolysis can be eliminated, for example, by treating with hydrogen in the presence of a catalyst (e.g. a precious metal catalyst such as palladium, expediently on a carrier such as carbon). In this context, suitable solvents those given above, in particular, for example, alcohols, such as methanol or ethanol or amides, such ae DMF. The hydrogenolysis is carried out, as a rule, at temperatures of between about 0 and 100° and pressures of between about 1 and 200 bar, preferably at 20-30° and 1-10 bar. Hydrogenolysis of the - to -CBZ group is achieved satisfactorily, for example, on 5-10~ Pd-C in methanol at 20-30°.
Compounds of the formula I can preferably also be obtained by reacting a compound of the formula II with a base of the formula III. The knows methods of N-alkyla-tioa are then expediently utilized.
The leaving group E is preferably C1, Br, I, C1-C6-alkylsulfonyloxy, such as methanesulfonyloxy or ethanesulfoayloxy, or C6-Cl°-arylsulfoayloxy, such as benzenesulfonyloxy, p-toluenesulfonyloxy or 1- or 2-naph-thalenesulfonyloxy.
The reaction is preferably effected in the presence of an additional base, e.g. of an alkali metal or alkaline earth metal hydroxide or carbonate. such as sodium, potassium or calcium hydroxide, or sodium, potassium or calcium carbonate, is an inert solvent, e.g.
a halogeaated hydrocarbon, such as dichloromethane, an ether, such as THF or dioxane, an amide, such as DMF or dimethylacetamide, or a nitrile, such as acetonitrile, at temperatures of between about '-20 and 200, preferably between 0 and 120°. If the leaving group E of I is differeeat, the addition of an iodide, such as potassium iodide, is advisable.
The starting compounds of the formula II are novel, as a rule. They can be prepared, for example, by reacting a substituted aniline of the formula R1-NHs with a compound of the formula RSCHs-CHIt6-CHzOH (where RS is E, R6 is XR', R' is a protective group, and RS and R6 together are also O) to give a compound of the formula Rl-N8-CHz-CHR°-CHsOH (where R° is XR' or OH), where appro-priate eliminating the protective group R' to give com-pounds of the formula Rl-NH-CH,-CH (7~) -CSs08, reacting with a derivative of carbonic acid, such as diethyl carbonate, to give 3-R1-5-hydroxymethyl-2-oxazolidinones, and converting the hydroxymethyl group into a CHsE group, e.g. using SOCls, SOBrz, methaaesulfonyl chloride or p-tolueaesulfonyl chloride. The compounds of the formula H-Y (III) are known, as a rule, or can be prepared in analogy with knows compounds.

- 11 _ In addition, compounds of the formula I can be obtained by reacting a compound of the formula IV (or a reactive derivative thereof) with a reactive derivative of carbonic acid.
Suitable carbonic acid derivatives are, in particular, dialkyl carbonates, such as diethyl carbonate, and, additionally, alkyl esters of chloro-formic acid. such as ethyl chlorofoz~ate. Preferably, the carbonic acid derivative, which is expediently employed in excess, also serves as a solvent or suspending agent.
One of the given solvents can be present as well, provided it is inert is this reaction. Furthermore, the addition of a base is advisable, in particular of an alkali metal alcoholate, such as potassium tert-butylate.
Reaction temperatures of between 0 and 150°, preferably of between 70 and 120°, are expediently employed The starting compounds of the formula IV are novel, as a rule. They can be obtained., .for example, by functionalizing the abovementioned compounds of the formula R1-NH-CHz-CH (~) -CHzOH to 'give compounds of the formula Rl-NH-CHz-CH (XH) -CHz-E cad reacting with compounds of the formula H-Y . (III) .
In order to prepare compounds of the formula I, in which Rl is a guanidinophenyl group, a corresponding aminophenyl compound can be treated with an amidiaating agent. 1-Amidino-3,5-dimethylpyrazol which is, in parti-cular, employed is particular in the fox~n of its nitrate, is preferred as as amidinating agent. The reaction is expediently carried out in the presence of a base, such as triethylamine or ethyl diisopropylamine, in an inert solvent or solvent mixture, e.g. water/dioxaae, at temperatures of between 0 cad 120°, preferably 60 and 120°.
It is furthermore possible, is a compound of the formula I, to convert one or both of the radicals Rl and/or Y into (an)other radicals) Rl and/or Y.
In particular, cyano groups can be reduced to aminomethyl groups, or converted into amidino groups or hydroxyamidino groups, carboxyl groups esterified, ester 2 ~ ~. ~ :i'~ ~.~
groups cleaved, beazyl groups removed hydrogeaolytically, and aminomethyl groups converted into guanidiaomethyl groups.
Reduction of cyano groups to aminomethyl groups is expediently effected by catalytic hydrogenation, e.g.
on Raney nickel at temperatures of between 0 and 100°, preferably 10 and 30°, and pressures of between 1 and 200 bar, preferably at atmospheric pressure, is an inert solvent, e.g. a lower alcohol, such as methanol or ethanol. expediently in the presence of ammonia. If the reaction is carried out, for example, at about 20° and 1 bar, benzyl ester groups or N-benzyl groups present in the starting material are then preserved. If it is desired to cleave these groups hydrogenolytically, a precious metal catalyst, preferably Pd-carbon, is then expediently used, it being possible to add an acid, such as acetic acid, and Water as well, to the solution.
In order to prepare an amidine of the formula I
(R1 = amidinophenyl), ammonia can be added onto a nitrile of the formula I (Rl = cyanophenyl). The addition is preferably effected in several steps, by, in a manner known per se, a) transforming the aitrile with°~$sS into a thioamide, which is converted with an alkylating agent, e.g. CH3I, into the corresponding S-alkyl imidothio eater, which latter reacts with NH3 to give the amidine, b) transforming the nitrile with as alcohol, e.g. ethanol in the presence of HCl, into the corresponding imido ester, and treating the latter with ammonia, or c) reac-ting the nitrite with lithium bis(trimethylsilyl)amide and subsequently hydrolysing the product.
The corresponding N-hydroxyamidines of the formula I (Rl = phenyl substituted by HO-NH-C(=NH)) can be obtained from the nitrites in an analogous manner if the work is carried out according to a) or b) but using hydroxylamine in place of ammonia.
For the esterification, as acid of the formula I
(R' = H) can be treated with an excess of alcohol of the formula R'-OH (R' - A or benzyl). expediently is the presence of a strong acid, such as hydrochloric acid or ~~.~..~~rl sulfuric acid, at temperatures of between 0 and 100, preferably 20 and 50°.
Conversely, an ester of the formula I (R' _ A or benzyl) can be converted into the corresponding acid of the formula I (R' - H), expediently by solvolysis in accordance with one of the abovementioned methods, e.g.
with NaOH or KOH in water/c'ioxane at temperatures of between 0 and 40°, preferably 10 and 30°.
A base of the formula I can be converted with an acid into the associated acid addition salt. Those acids, in particular, are suitable for this reaction which yield physiologically harmless salts. Thus, inorganic acids, e.g. sulfuric acid, nitric acid, hydrohalic acids, such as hydrochloric acid or hydrobromic acid, phosphoric acids, such as orthophosphoric acid, and sulfamic acid, and, in addition, organic acids, is particular aliphatic, alicyclic, araliphatic, aromatic or heterocyclic monobasic or polybasic carboxylic, sulfonic or sulfuric acids, e.g. formic acid, acetic,. acid, trifluoroacetic acid, propionic acid, pivalic acid, diethylacetic acid, malonic acid, succinic acid, pimelic acid, fumaric acid, malefic acid, lactic acid, tartaric acid, malic acid, citric acid, gluconic acid, ascorbic acid, nicotinic acid, isonicotinic acid, methanesulfoaic acid or ethane-sulfonic acid, ethanedisulfonic acid, 2-hydroxyethane-sulfonic acid, beazenesulfonic acid, p-toluenesulfoaic acid, aaphthalenemonosulfonic and naphthalenedisulfonic acids, and laurylsulfuric acid, can be used. Salts with acids with are not physiologically harmless, e.g.
picrates, may be used for isolating and/or purifying the compounds of the formula I.
The free bases of the formula I can, if desired, be liberated from their salts by treatiag with strong bases. such as sodium or potassium hydroxide, or sodium or potassium carbonate.
It is also possible to convert carboxylic acids of the formula I (R' - H) into their metal or ammonium salts, e.g. their sodium, potassium or calcium salts, by reaction with corresponding bases.

2~~~J~r1 The compounds of the formula I contain one or more chiral centres and can therefore be present in racemic or in optically active form. Racemates which are obtained can be resolved mechanically or chemically into the eaantiomers in accordance with methods which are known per se. Preferably, diastereomers are formed from the racemic mixture by reaction with an optically active resolving agent. Suitable resolving agents are, for example, optically active acids, such as the D and L
forms of tartaric acid, diacetyltartaric acid, dibenzoyl-tartaric acid, mandelic acid, malic acid or lactic acid, or the various optically active camphorsulfonic acids, such as /S-camphorsulfonic acid. Enantiomeric resolution using a column filled with an optically active resolving agent (e. g. dinitrobenzoylphenylglycine) is also advan-tageous; a mixture of hexane/isopropanol/acetonitrile, e.g. in the volume ratio of 82:15:3, is an example of a suitable eluent.
Naturally, it is also possible to obtain optically active compounds of the formula I in accordance with the above-described methods by using starting compounds (e.g. those of the formula II) which are already optically active.
The novel compounds of the formula I, and their physiologically harmless salts, may be used for producing pharmaceutical preparations by bringing them into a suitable dosage form together with at least one excipient or auxiliary agent, and, if desired, together with one or more additional active compound(s). The formulations thus obtained can be employed as pharmaceuticals in human or veterinary medicine. Those organic or inorganic compounds can be used as carrier substances which are suitable for enteral (e. g. oral or rectal) or parenteral adminis-tration, or for administration in the form of an inhalation spray. and do not react with the novel com-pounds, for example water, vegetable oils, benzyl alcohols. polyethylene glycols, glycerol triacetate and other fatty acid glycerides, gelatin, soybean lecithin, carbohydrates, such as lactose or starch, magnesium stearate, talc and cellulose. Tablets, coated tablets, capsules, syrups, juices or drops, in particular, can be employed for oral use; lacquered tablets and capsules possessing gastric juice-resistant coatings or capsule casings are of special interest. Suppositories caa be employed for rectal use, and solutions. preferably oily or aqueous solutions, and, additionally, suspensions, emulsions or implants, for parenteral administration.
For administration as an inhalation spray, sprays can be used which contain the active substance either dissolved or suspended in a propellaat gas mixture.
Expediently the active compound is then used is micro nized form, it being possible for one or more additional physiologically tolerated solvents. e.g. ethanol, to be present. Inhalation solutions can be administered using customary inhalers. The novel compounds can also be lyophilized and the resulting lyophilizates be used, for example, for producing injection preparations. The given formulations can be sterilized and/or contain auxiliary agents, such as preservatives, stabilizers and/or wetting agents, emulsifiers, salts for affecting the osmotic pressure, buffering substances, and colorants and/or fragrances. They may, if desired, also contain one or more additional active compounds, e.g. one or more vitamins.
The substances according to the invention are administered. as a rule, in aaalogy with other known and commercially available pharmaceuticals, in particular, however, in analogy with the compounds described in EP-A-459256, preferably is dosages between about 5 mg and 1 g, is particular between 50 and 500 mg, per dosage unit. The daily dosage is preferably between about 0.1 and 20 mg/kg, in particular 1 and 10 mg/kg, of body weight. However, the specific dose for each particular patient depends on a wide variety of factors, for example the activity of the specific compound employed. on age, body weight, general health, and sex. on the food, on the time and route of administration, on the speed of ex-cretion, on the combination of medicines employed, and on 21 ~ ~ j'~ ~.

the severity of the particular disease to which the therapy applies. Oral administration is preferred.
Ia the above and that which follows, all tempera tures are given in °C. In the examples below, "customary working-up" means: if necessary, Water is added, pH
values are adjusted to between 2 and 8 depending on the constitution of the end product, extraction takes place with ethyl acetate or dichloromethane, the phases are separated, the organic phase is dried over sodium sulfate and evaporated, and purification is then effected by chromatography on silica gel and/or by crystallization.
FAB = (M' + 1) peak in the mass spectrum, obtained by the "fast-atom bombardment" method.
Example 1 A solution of 1 g of ethyl 1-tert-butoxycarbonyl-4-(3-(4-cyanophenyl)-2-oxo-5-oxazolidiaylmethyl)-piperaziae-2-carboxylate (obtainable by reacting 3-(4-cyanophenyl)-5-bromomethyl-2-oxazolidinone with ethyl 1-tert-butoxycarbonylpiperazine-2-carboxylate in accordance With the method described is Example 3) in 12 ml of dichloromethaae and 12 ml of trifluoroacetic acid is left to stand at 20° for 1 h. and they concen trated by evaporation. Ethyl 1-(3-(4-cyanophenyl)-2-oxo 5-oxazolidinylmethyl)piperazine-3-carboxylate is obtained, FAB 359.
1-(3-(4-cyaaophenyl)-2-oxo-5-oxazolidinylmethyl)-piperaziae-3-carboxylic acid, and its benzyl ester, is obtained is an analogous manner from 1-tert-butoxy-carbonyl-4-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinyl-methyl)piperazine-2-carboxylic acid, or its benzyl ester.
Example 2 A solution of 1 g of tert-butyl 1- (3- (4-benzyl-oxycarbonylaminomethylphenyl)-2-oxo-5-oxazolidiayl-methyl)piperidine-4-oxyacetate (obtaiaa~ble from 3-(4-beazyloxycarbonylamiaomethylphenyl)-5-chloromethyl-2-oxazolidinone and tent-butyl piperidine-4-oxyacetate in accordance with the method described in Example 3) in a mixture of 38 ml of methanol, 6 ml of water and 6 ml of acetic acid is hydrogenated on 0.6 g of 5% Pd-carbon at ~~;~;;,~''l_i.

20° and 1 bar until H~ uptake has ceased. The mixture is filtered and the filtrate is concentrated by evaporation, and tart-butyl 1-(3-(4-aminomethylphenyl)-2-oxo-5-oxa-zolidinylmethyl)piperidine-4-oxyacetate is obtained, m.p. 95-96°, FAB 420.
Example 3 A mixture of 2.96 g of 3-(4-cyanophenyl)-5-methanesulfonyloxymethyl-2-oxazolidinone (m. p. 162-163°; obtainable by reacting 4-aminobenzonitrile with 2,3-epoxypropanol to give 4-(2,3-dihydroxypropylamino)-beazonitrile (oily), reacting with diethyl carbonate/
potassium tert-butylate at 110° to give 3-(4-cyan-ophenyl)-5-hydroxymethyl-2-oxazolidiaone (m.p. 130-131°) and esterifying with methanesulfonyl chloride), 1.69 g of ethyl piperidine-4-carboxylate, 70 ml of acetonitrile, 1.38 g of potassium carbonate and 1.65 g of potassium iodide is boiled for 25 h. After customary working up, ethyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinylmethyl)-piperidiae-4-carboxylate ("IA") is obtained, FA8 358.
The following are obtained~in an analogous manner:
with benzyl piperidine-4-carboxylate:
benzyl 1-(3-(4-cyanopheayl)-2-oxo-5-oxazolidinyl methyl)piperidine-4-carboxylate, m.p. 96°, FAB 420;
with tert-butyl piperidine-4-carboxylate:
tart-butyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidia-ylmethyl)piperidiae-4-carboxylate;
with ethyl piperidine-3-carboxylate:
ethyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidiayl-methyl)piperidine-3-carboxylate;
with benzyl piperidine-3-carboxylate:
benzyl 1-(3-(4-cyanopheayl)-2-oxo-5-oxazolidinyl-methyl)piperidine-3-carboxylate, FAB 420;
with tert-butyl piperidine-3-carboxylate:
tert-butyl 1-(3-(4-cyanophenyl)-2-oxo-5.-oxazolidin-ylmethyl)piperidine-3-carboxylate;
with ethyl piperidine-2-carboxylate:
ethyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinyl-methyl)piperidiae-2-carboxylate;
with benzyl piperidine-2-carboxylate:

2~2~c~r~~

benzyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinyl-methyl)piperidine-2-carboxylate, FAB 420;
with tart-butyl piperidine-2-carboxylate:
tent-butyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxaznlidin-ylmethyl)piperidine-2-carboxylate;
with ethyl pyrrolidine-2-carboxylate:
ethyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinyl-methyl)pyrrolidine-2-carboxylate;
with benzyl pyrrolidine-2-carboxylate:
benzyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinyl-methyl)pyrrolidine-2-carboxylate;
with tart-butyl pyrrolidine-2-carboxylate:
tart-butyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidin-ylmethyl)pyrrolidine-2-carboxylate;
15. with ethyl piperidine-4-acetate:
ethyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazola:dinyl-methyl)piperidine-4-acetate;
with benzyl piperidine-4-acetate:
benzyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinyl-methyl)piperidine-4-acetate;
with tart-butyl piperidine-4-acetate:
tart-butyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidin-ylmethyl)piperidine-4-acetate;
with ethyl piperidine-4-oxyacetate:
ethyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinyl-methyl)piperidine-4-oxyacetate;
With benzyl piperidine-4-oxyacetate:
benzyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinyl-methyl)piperidine-4-oxyacetate;
with tart-butyl piperidine-4-oxyacetate:
tart-butyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidia-ylmethyl)piperidine-4-oxyacetate, m.p. 88-89°;
FAB 416;
with ethyl piperidine-3-oxyacetate:
ethyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinyl-methyl)piperidine-3-oxyacetate;
with benzyl piperidine-3-oxyacetate:
beazyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinyl-methyl)piperidine-3-oxyacetate;

~1~~ ~ ;J.~

with tart-butyl piperidine-3-oxyacetate:
tart-butyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidin-ylmethyl)piperidiae-3-oxyacetate;
with ethyl piperazine-1-acetate:
ethyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinyl-methyl)pipesazine-4-acetate;
with benzyl piperazine-1-acetate:
benzyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinyl-methyl)piperazine-4-acetate;
with tart-butyl piperazine-1-acetate:
tart-butyl 1-(3-(4-cyanopaenyl)-2-oxo-5-oxazolidin- .
ylmethyl)piperazine-4-acetate;
with ethyl azetidine-3-oxyacetate:
ethyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinyl-methyl)azetidine-3-oxyacetate;
with benzyl azetidine-3-oxyacetate:
benzyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinyl-methyl)azetidine-3-oxyacetate;
with test-butyl azetidine-3-oxyacetate:
tart-butyl 1-(3-(4-cyanopheayl)-2-oxo-5-oxazolidin-ylanethyl)azetidine-3-oxyacetate;
with ethyl 1-benzylpiperazine-2-carboxylate:
ethyl 1-benzyl-4-(3-(4-cyanopheayl)-2-oxo-5-oxa-zolidinyl)piperazine-2-carboxylate;
with benzyl 1-benzylpiperazine-2-carboxylate:
benzyl 1-benzyl-4-(3-(4-cyanopheayl)-2-oxo-5-oxa-zolidinyl)piperazine-2-carboxylate;
with tent-butyl 1-benzylpigerazine-2-carboxylate:
tart-butyl 1-benzyl-4-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinyl)piperazine-2-carboxylate.
The following is obtained in an analogous manner by the reaction of 3-(4-cyanopheayl)-5S-methanesul-foayloxymethyl-2-oxazolidinone (m.p. 141-142°; [a~DO
+75.3° (c = 3.9 mg/ml in methanol); obtainable by reacting 4-aminobenzonitrile with 2R-2,3-epoxypropanol to give 4-(25.3-dihydroxypropylamino)beazonitrile, reacting with diethyl carbonate/potassium tart-butylate to give 3-(4-cyanophenyl)-5S-hydroxymethyl-2-oxazolidinone and est~rifying with methanesulfonyl chloride) with benzyl piperidine-4-carboxylate:
benzyl 1-(3-(4-cyanophenyl)-2-oxo-5S-oxazolidinyl-methyl)piperidine-4-carboxylate, m.p. 87-88°, [aJD°
43.0° (c = 9.8 mg/ml in methanol).
The following are obtained in an analogous manner with ethyl piperidine-4-carboxylate:
ethyl 1-(3-(4-cyanophenyl)-2-oxo-5S-oxazolidinyl-methyl)piperidine-4-carboxylate;
with tent-butyl piperidine-4-carboxylate:
tart-butyl 1-(3-(4-cyanophenyl)-2-oxo-5S-oxazolidin-ylmethyl)piperidine-4-carboxylate.
Beazyl 1-(3-(4-cyanophenyl)-2-oxo-5R-oxa-zolidinylmethyl)piperidine-4-carboxylate and the corres ponding ethyl ester and the corresponding tert-butyl ester are obtained in an analogous manner from 3-(4-cyanophenyl)-5R-methanesulfoayloxymethyl-2-oxazoli-dinone (obtainable from 2S-2,3-epoxypropanol via 4-(2R, 3-dihydroxypropylamino)benzonitrile and 3-(4-cyano-pheayl)-5R-hydroxymethyl-2-oxazolidinone).
Example 4 In analogy with Example 3, tert-butyl 1-(3-(4-dimethylaminomethylphenyl)-2-oxo-5-oxazolidinyl-methyl)piperidine-4-carboxylate, FAB 432, ie obtaiaed from the ,reaction of 3-(4-dimethylaminomethylphenyl)-5-bromomethyl-2-oxazolidinone (obtainable by reacting 4-dimethylaminomethylaniline with 2,3-epoxypropanol to give 3-(4-dimethylaminomethylphenylamiao)-1,2-propane-diol, reacting with diethyl carboaate/potassium tert-butylate to give 3-(4-dimethylaminomethylphenyl)-5-hydroxymethyl-2-oxazolidinone and reacting with SOBr,) with tent-butyl piperidine-4-carboxylate.
Example 5 A mixture of 3.31 g of ethyl 1-(3-(4-cyano-phenyl)-2-hydroxypropyl)piperidine-4-carboxylate (obtain-able by reacting 3-(4-cyanophenyl)-1,2-propanediol-1-methanesulfonate with ethyl piperidiae-4-carboxylate), 15 ml of diethyl carbonate and 0.1 g of potassium tert-butylate is stirred at a bath temperature of 110° for 2 h. The mixture is concentrated by evaporation, worked 2~.~~~~~ ~.

up is the customary manner, gad "IA" , FAH 358, is obtained.
Example 6 0.17 ml of ethyl diisopropylamine is added to a solution of 201 mg of 1-amidino-3,5-dimethylpyrazole nitrate in 17 ml of dioxaae and 5 ml of water, and the mixture is stirred for 15 min. 375 mg of tert-butyl 1-(3-(4-aminophenyl)-2-oxo-5-oxazolidinylmethyl)piper-idiae-4-carboxylate (obtainable by reacting 4-aminoacet-anilide with 2,3-epoxypropanol to give 4-(2,3-dihydroxy-propylamiao)acetanilide, reacting with diethyl carboaate to give 3-(4-acetamidophenyl)-5-hydroxymethyl-2-oxazoli-dinone, converting into the methaaesulfonate and reacting with tert-butyl piperidiae-4-carboxylate) are then added, and the mixture is then boiled for 45 h., concentrated by evaporation and worked up in the customary meaner, and tert-butyl 1-(3-(4-guaaidinophenyl)-2-oxo-5-oxazolidinyl-methyl)piperidine-4-carboxylate is obtained.
tert-Butyl 1-(3-(4-guanidinomethylphenyl)-2-oxo 5-oxazolidinylmethyl)piperidine-4=carboxylate, FAB 432, is obtained in an analogous manger ~rom the reaction of tert-butyl 1-(3-(4-aminomethylphenyl)-2-oxo-5-oxazo lidiaylmethyl)piperidine-4-carboxylate~ and 1-amidino 3,5-dimethylpyrazole nitrate.
Example 7 A solution of 1 g of "IA" in 40 ml of 10%
methaaolic NS, solution is hydrogenated on 0.6 g of Raney Ni at 20° gad 1 bar until Hz uptake is complete.
Following filtration and concentration by evaporation, ethyl 1-(3-(4-aminomethylphenyl)-2-oxo-5-oxazolidinyl-methyl)piperidine-4-carboxylate, FAB 362, is obtained.
The following 1-(3-(4-aminomethylphenyl)-2-oxo-5-oxazolidiaylmethyl)piperidines are obtained is an analogous meaner by hydrogenating the corresponding aitriles:
-4-carboxylic acid tert-butyl ester -3-carboxylic acid ethyl ester -3-carboxylic acid tert-butyl ester -2-carboxylic acid ethyl ester 2~~~~~ ~_ -2-carboxylic acid tert-butyl ester -4-acetic acid ethyl ester -4-acetic acid tert-butyl ester -4-oxyacetic acid ethyl ester -4-oxyacetic acid tert-butyl ester, m.p. 95-96°, -3-oxyacetic acid ethyl ester -3-oxyacetic acid tert-butyl ester;
as are the following 1-(3-(4-aminamethylphenyl)-2-oxo-5-oxazolidinylmethyl)pyrrolidines:
-2-carboxylic acid ethyl ester -2-carboxylic acid tent-butyl ester;
as are the following 1-(3-(4-aminomethylphenyl)-2-oxo-5-oxazolidinylmethyl)piperazines:
-4-acetic acid ethyl ester -4-acetic acid tent-butyl ester;
as are the following 1-(3-(4-amiaomethylphenyl)-2-oxo-5-oxazolidinylmethyl)azetidines:
-3-oxyacetic acid ethyl ester -3-oxyacetic acid tert-butyl. ester;
as are the following 1-(3-(4-aminomethylphenyl)-2-oxo-5-oxazolidinylmethyl)-4-benzylpiperazines:
-3-carboxylic acid ethyl ester -3-carboxylic acid tert-butyl ester;
as are the following 1-(3-(4-aminomethylphenyl)-2-oxo-5S-oxazolidinylmethyl)piperidines:
-4-carboxylic acid ethyl ester -4-carboxylic acid tert-butyl ester;
as are the following 1-(3-(4-amiaomethylphenyl)-2-oxo-5R-oxazolidinylmethyl)piperidines:
-4-carboxylic acid ethyl ester -4-carboxylic acid tert-butyl ester.
Example 8 HsS is passed (45 min) at -10° into a~solutioa of 3.57 g of "IA" in 50 ml of pyridine and 6.6 ml of triethylamine. Subsequently, the mixture is stirred at 20° for 14 h and then concentrated by evaporation; the residue is dissolved in 50 ml of acetone and 9 ml of methyl iodide are added to this solution. After stirring ~~~~~ J'%' ._ at 20° for 6 hours, filtering off takes place and the residue is washed with a little acetone and dissolved in 30 ml of methanol; 4.6 g of ammonium acetate are then added and the mixture is stirred at 20° for 30 h. The resulting ethyl 1-(3-(4-amidinophenyl)-2-oxo-5-oxazoli-dinylmethyl)piperidine-4-carboxylate is filtered off and chromatographed on silica gel (dichloromethane/methanol/
acetic acid 70:30:2); m.p. 200° (decomp.); FAB 375.
Thefollowing 1-(3-(4-amidinopheayl)-2-oxo-5-oxa zolidinylmethyl)piperidines are obtained in an analogous manner from the corresponding nitriles:
-4-carboxylic acid benzyl ester. m.p. 204°
(decomp.); FAB 437; dihydrochloride m.p. 182°
-4-carboxylic acid tert-butyl ester -3-carboxylic acid ethyl ester -3-carboxylic acid benzyl ester, acetate. FAB 437 -3-carboxylic acid tert-butyl ester -2-carboxylic acid ethyl ester -2-carboxylic acid benzyl ester, FAB 437 -2-carboxylic acid tert-butyl ester -4-acetic acid ethyl ester -4-acetic acid benzyl ester -4-acetic acid tent-butyl ester -4-oxyacetic acid ethyl ester -4-oxyacetic acid benzyl ester, acetate, m.p. 206°
-4-oxyacetic acid tert-butyl ester, m.p. 187°
(decomp.); FAB 433 -3-oxyacetic acid ethyl ester -3-oxyacetic acid benzyl ester -3-oxyacetic acid tart-butyl ester;
as are the following 1-(3-(4-amidiaophenyl)-2-oxo-5-oxa-zolidinylmethyl)pyrrolidines:
-2-carboxylic acid ethyl ester -2-carboxylic acid benzyl ester -2-carboxylic acid tert-butyl ester;
ae are the following 1-(3-(4-amidinophenyl)-2-oxo-5-oxa-zolidinylmethyl)piperazines:
-4-acetic acid ethyl ester -4-acetic acid benzyl ester, FAB 452 -4-acetic acid tart-butyl ester;
as are the following 1-(3-(4-amidinophenyl)-2-oxo-5-oxa-zolidinylmethyl)azetidines:
-3-oxyacetic acid ethyl ester -3-oxyacetic acid benzyl ester -3-oxyacetic acid tart-butyl ester;
as are the following 1-(3-(4-amidinophenyl)-2-oxo-5-oxa-zolidinylmethyl)-4-benzylpiperazines:
-3-carboxylic acid ethyl ester -3-carboxylic acid benzyl ester -3-carboxylic acid tart-butyl ester;
as are the following 1- (3- (4-amidiaophenyl) -2-oxo-5S-oxa-zolidinylmethyl)piperidines:
-4-carboxylic acid ethyl ester -4-carboxylic acid benzyl ester -4-carboxylic acid tart-butyl ester;
as are the following 1-(3-(4-amidinophenyl)-2-oxo-5R-oxa-zolidinylmethyl)piperidines:
-4-carboxylic acid ethyl ester -4-carboxylic acid beazyl ester -4-carboxylic acid tart-butyl ester.
Example 9 Ethyl 1-(3-(4-hydroxyamidiaophenyl)-2-oxo-5-oxazolidinylmethyl)piperidiae-4-carboxylate is obtained from "IA" is analogy with Example 8, but usiag an equi-valent quantity of hydroxylaamnonium acetate instead of ammoaium acetate. .
Example 10 1 g of tart-butyl (1-(3-(4-cyanophenyl)-2-oxo- ..
5-oxazolidiaylmethyl)piperidine-4-carboxylate is dis-solved in 12 ml of dichloromethane, sad 12 ml of tri-fluoroacetic acid are they added; the mixture is left to stead for 5 min., concentrated by evaporation and worked up in the customary manner; 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinylmethyl)piperidine-4-carboxylic acid, FAB 330, is obtaiaed.
The following acids are obtained in an aaalagous meaner from the corresponding tart-butyl esters:
1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinylmethyl)-.. , - 2 ~ ~ s.a ;.~ 3 i .L
piperidine-3-carboxylic acid 1-(3-(4-cyanophenyl)-2-oxo-5-axazolidinylmethyl)-piperidine-2-carboxylic acid 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinylmethyl)pyrrol-idine-2-carboxylic acid 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinylmethyl)-piperidine-4-acetic acid 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinylmethyl)-piperidine-4-oxyacetic acid 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinylmethyl)-piperidine-3-oxyacetic acid 1-(3-(4-cyaaophenyl)-2-oxo-5-oxazolidinylmethyl)-piperazine-4-acetic acid 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinylmethyl)-azetidine-3-oxyacetic aeid 1-benzyl-4-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinyl-methyl)piperaziae-2-carboxylic acid 1-(3-(4-amiaomethylphenyl)-2-oxo-5-oxazolidinylmethyl)-piperidiae-4-carboxylic acid, m.p. 190° (decomp.):

1-(3-(4-aminomethylphenyl)-2-oxo-5-oxazolidinylmethyl)-piperidiae-3-carboxylic acid 1-(3-(4-aminomethylphenyl)-2-oxo-5-oxazolidinylmethyl)-piperidiae-2-carboxylic acid 1-(3-(4-amiaomethylphenyl)-2-oxo-5-oxazolidinylmethyl)-pyrrolidine-2-carboxylic acid 1-(3-(4-aminomethylphenyl)-2-oxo-5-oxazolidinylmethyl)-piperidine-4-acetic acid l-(3-(4-aminomethylphenyl)-2-oxo-5-oxazolidinylmethyl)-piperidine-4-oxyacetic acid, m.p. 135°: FAB 364 1-(3-(4-amiaomethylphenyl)-2-oxo-5-oxazolidinylmethyl)-piperidine-3-oxyacetic acid 1-(3-(4-amiaomethylphenyl)-2-oxo-5-oxazolidiaylmethyl)-piperazine-4-acetic acid 1-(3-(4-aminomethylphenyl)-2-oxo-5-oxazolidinylmethyl)-azetidine-3-oxyacetic acid 1-beazyl-4-(3-(4-aminomethylphenyl)-2-oxo-5-oxazolidin-ylmethyl)piperazine-2-carboxylic acid 1-(3-(4-amidinophenyl)-2-oxo-5-oxazolidinylmethyl)piper-~~~~~~i idine-4-carboxylic acid, m.p. 265° (decomp.); FAB 347;
dihydrochloride, m.p. 142°
1-(3-(4-amidinophenyl)-2-oxo-5-oxazolidinylmethyl)piper-idine-3-carboxylic acid 1-(3-(4-amidinopheayl)-2-oxo-5-oxazolidiaylmethyl)piper-idine-2-carboxylic acid, m.p. 198°; FAB 347 1-(3-(4-amidinophenyl)-2-oxo-5-oxazolidinylmethyl)pyrrol-idine-2-carboxylic acid 1-(3-(4-amidinophenyl)-2-oxo-5-oxazr~lidinylmethyl)piper-idine-4-acetic acid, m.p. 256°
1-(3-(4-amidinophenyl)-2-oxo-5-oxazolidinylmethyl)piper-idine-4-oxyacetic acid, oil, FAB 377 1-(3-(4-amidinophenyl)-2-oxo-5-axazolidinylmethyl)piper-idine-3-oxyacetic acid, m.p. 167-168°
1-(3-(4-amidiaophenyl)-2-oxo-5-oxazolidinylmethyl)piper-azine-4-acetic acid, FAB 362 1-(3-(4-amidiaophenyl)-2-oxo-5-oxazolidinylmethyl)azet-idine-3-oxyacetic acid 1-benzyl-4-(3-(4-amidinophenyl)-.2-oxo-5-oxazolidinyl-methyl)piperazine-2-carboxylic acid 1-(3-(4-guanidinophenyl)-2-oxo-5-oxazolidinylmethyl)-piperidine-4-carboxylic acid 1-(3-(4-guanidinomethylphenyl)-2-oxo-5-oxazolidinyl-methyl)piperidine-4-carboxylic acid, FAB 376 1-(3-(4-cyanophenyl)-2-oxo-5S-oxazolidinylmethyl)-piperidine-4-carboxylic acid 1-(3-(4-cyanophenyl)-2-oxo-5R-oxazolidinylmethyl)-piperidine-4-carboxylic acid 1-(3-(4-aminomethylphenyl)-2-oxo-5S-oxazolidinylmethyl)-piperidine-4-carboxylic acid 1-(3-(4-~s.nomethylphenyl)-2-oxo-5R-oxazolidinylmethyl)-piperidiae-4-carboxylic acid 1-(3-(4-amidinomethylphenyl)-2-oxo-5S-oxazolidinyl-methyl)piperidine-4-carboxylic acid 1-(3-(4-amidinomethylphenyl)-2-oxo-5R-oxazolidinyl-methyl)piperidine-4-carboxylic acid 1-(3-(4-dimethylaminomethylphenyl)-2-oxo-5-oxazolidinyl-methyl)piperidine-4-carboxylic acid.

2~~<~~'~' Example 11 A solution of 1 g of benzyl 1-(3-(4-amidino-phenyl)-2-oxo-5-oxazolidinylmethyl)piperidine-4-carboxy-late in 100 ml of methanol, 17 ml of acetic acid and 17 ml of water is hydrogenated on 0.7 g of 5~ Pd-carbon at 20° and 1 bar until hydrogen uptake has ceased. The mixture is filtered and concentrated by evaporation, and the residue is triturated with diethyl ether, with 1-(3-(4-amidinophenyl)-2-oxo-5-oxazolidinylmethyl)piper-idine-4-carboxylic acid being obtained, m.p. 265°;
FAB 347; dihydrochloride, m.p. 142°.
Example 12 1-(3-(4-Aminomethylphenyl)-2-oxo-5-oxazolidinyl-methyl)piperazine-3-carboxylic acid is obtained in analogy with Example 11 by the hydrogenation of 1-beazyl - 4-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinylmethyl)piper azine-2-carboxylic acid ("IB"; or of "IB" benzyl ester).
The same substance can be obtained in an analo gous manner by the hydrogenation of 1-benzyl-4-(3-(4 aminomethylphenyl)-2-oxo-5-oxazolidinylmethyl)piperazine 2-carboxylic acid (or of its benzyl ester).
Ethyl 1-(3-(4-aminomethylphenyl)-2-oxo-5-oxazo-lidinylmethyl)piperazine-3-carboxylate and tert-butyl 1-(3-(4-aminomethylphenyl)-2-oxo-5-oxazolidinylmethyl)-piperazine-3-carboxylate are obtained in an analogous manner from the ethyl and tert-butyl esters of "IB", respectively.
Example 13 The following are obtained by analogy with Example 3 from 3-(4-cya,nophenyl)-5-methanesulfonyloxy methyl-2-oxazolidinone:
with benzyl piperidine-3-acetate:
beazyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinyl-methyl)piperidine-3-acetate, FAB 434 with methyl 3-(1-piperazinyl)propionate:
methyl (3-(4-(3-(4-cyanophenyl)-2-oxo-5-oxazolidin-ylmethyl)-1-piperazinyl)propioaate, FAB 373 with ethyl 3-(1-piperazinyl)propionate:
ethyl 3-(4-(3-(4-cyanopheayl)-2-oxo-5-oxazolidinyl-~1~~,5"t _., - 28 -methyl)-1-piperazinyl)propionate, FAB 387 with ethyl 2-oxopiperazin-1-acetate:
ethyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinyl-methyl)-3-oxo-piperazine-4-acetate, FAB 387 with ethyl 3-(2-oxo-1-piperazinyl)propionate:
ethyl 3-(4-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinyl-methyl)-2-oxo-1-piperazinyl)-propionate, FAB 401 with ethyl 4-hydroxypiperidine-4-carboxylate:
ethyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinyl- .
methyl)-4-hydroxypiperidine-4-carboxylate, FAB 374 with ethyl 4-hydroxypiperidine-4-acetate: w ethyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinyl-methyl)-4-hydroxypiperidine-4-acetate, FAR 388 with 1-oxa-8-azaspiro [4.5] decan-2-one (= lactone of 3- (4-hydroxy-4-piperidyl)propionic acid):
8-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinylmethyl)-1-oxa-8-azaspiro[4.5]decan-2-one, FA8 356.
The following are obtained analogously from 3-(4-cyano phenyl)-5R- or -5S-methanesulfonyloxymethyl-2-oxazolidi none:
with benzyl piperidine-4-carboxylate:
benzyl 1-(3-(4-cyanophenyl)-2-oxo-5R-oxazolidinyl-methyl)piperidine-4-carboxylate benzyl 1-(3-(4-cyanophenyl)-2-oxo-5S-oxazolidinyl-methyl)piperidine-4-carboxylate with ethyl piperazine-4-acetate:
ethyl 1-(3-(4-cyanophenyl)-2-oxo-5R-oxazolidinyl-methyl)piperazine-4-acetate, FAB 373 ethyl 1-(3-(4-cyanophenyl)-2-oxo-5S-oxazolidinyl-methyl)piperazine-4-acetate, FAB 373 with benzyl 3-(1-piperazinyl)propionate benzyl 3-(4-(3-(4-cyanophenyl)-2-oxo-5R-oxa-zolidinylmethyl)-1-piperazinyl)propionate, m.p. 90°
benzyl 3-(4-(3-(4-cyanophenyl)-2-oxo-5S-oxazo-lidinylmethyl)-1-piperazinyl)propionate, m.p. 90°.
Example 14 The following are obtained by analogy with Example 8 from the corresponding nitriles (see Example z~~~~~~.

13) benzyl 1-(3-(4-amidinophenyl)-2-oxo-5-oxazolidinyl-methyl)piperidine-3-acetate, diacetate, m.p.
287-288°
ethyl 3-(4-(3-(4-amidinophenyl)-2-axo-5-oxazo-lidinylmethyl)-1-piperazinyl)propionate, m.p. 206°
ethyl 1-(3-(4-amidinophenyl)-2-oxo-5-oxazolidinyl-methyl)-3-oxo-piperazine-4-acetat, m.p. 224°
ethyl 3-(4-(3-(4-amidinophenyl)-2-oxo-5-oxazoli-dinylmethyl)-2-oxo-1-piperazinyl)propionate, FAB 418 ethyl 1-(3-(4-amidinophenyl)-2-oxo-5-oxazolidinyl-methyl)-4-hydroxypiperidine-4-carboxylate ethyl 1-(3-(4-amidinophenyl)-2-oxo-5-oxazolidinyl-methyl)-4-hydroxypiperidine-4-acetate,acetate, m.p.
108°
8-(3-(4-ama.dinophenyl)-2-oxo-5-oxazolidinylmethyl)-1-oxa-8-azaspiro-[4.5]decan-2-one, FAB 373 benzyl 1-(3-(4-amidinophenyl)-2-oxo-5R-oxazolidinyl methyl)piperidine-4-carboxylate, acetate, m.p. 225° Ia]D +40.5° (c =~1, methanol) benzyl 1-(3-(4-amidinophenyl)-2-oxo-5S-oxazolidinyl-methyl)piperidine-4-carboxylate, acetate, m.p. 225° [a]D -41° (c = 1, methanol) ethyl 1-(3-(4-amidinophenyl)-2-oxo-5R-oxazolidinyl-methyl)piperazine-4-acetate, FAB 390 ethyl 1-(3-(4-amidinophenyl)-2-oxo-5S-oxazolidinyl-methyl)piperazine-4- acetate. FAB 390.
Example 15 The following are obtained by analogy with Example 9 from the corresponding nitrites:
ethyl 1-(3-(4-hydroxyamidiaopheayl)-2-oxo-5-oxazoli-dinylmethyl)-4-hydroxypiperidine-4-acetate, acetate, m.p. 178-180°
methyl 3-(4-(3-(4-hydroxyamidinophenyl)-2-oxo-5 oxazolidinylmethyl)-1-piperazinyl)propionate, m.p. 202°
benzyl 3-(4-(3-(4-hydroxyamidinophenyl)-2-oxo-5R-oxazolidinylmethyl)-1-piperazinyl)propioaate, m.p. 159°

benzyl 3-(4-(3-(4-hydroxyamidinophenyl)-2-oxo-5S-oxazolidinylmethyl)-1-piperazinyl)propionate, m.p. 159°
Example 16 A mixture of 1 g of ethyl 3- (4- (3- (4-amidino-pheayl)-2-oxo-5-oxazolidiaylmethyl)-1-piperazinyl)propio-hate, 0.2 g of NaOH; 8 ml of dioxane and 2 ml of water is .
stirred at 20° for 5 hours. After acidification and conventional work-up, 3-(4-(3-(4-amidinophenyl)-2-oxo-5-oxazolidinylmethyl)-1-piperazinyl)propionie acid, m.p.
269°, is obtained.
The following are obtained analogously by hydro-lysis of the corresponding esters:
1-(3-(4-amidinophenyl)-2-oxo-5-oxazalidinylmethyl)-3-oxo-piperazine-4-acetic acid, monohydrate, m.p. 261°
3-(4-(3-(4-amidinophenyl)-2-oxo-5-oxazolidinyl- .
methyl)-2-oxo-1-piperazinyl)propionic acid, FAB 390 1-(3-(4-amidinophenyl)-2-oxo-5-oxazolidinylmethyl)-4-hydroxypiperidine-4-carboxylic acid 1-(3-(4-amidinophenyl)-2-oxo-5-oxazolidinylmethyl)-4-hydroxypiperidine-4-acetic acid, m.p. 230°
1-(3-(4-amidinophenyl)-2-oxo-5R-oxazolidinylmethyl)-piperazine-4-acetic acid, acetate, FAB 362, (a)Do -28.0° (c = 1, DMSO) 1-(3-(4-amidinophenyl)-2-oxo-5S-oxazolidinylmethyl)-piperazine-4-acetic acid, acetate, FAB 362, (a]D°
+24.0° (c = l, DMSO) Example 17 a) 1 g of ethyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazo-lidinylmethyl)-4-methanesulfonyloxypiperidine-4-acetate (obtainable from the 4-hydroxy compound (see Example 13) with methanesulfonyl chloride/pyridine) is dissolved in a 2 ~ NH3 solution in l0~ml of a 1:1 mixture of ethanol and TFiF, and the solution ie left to stand at 20° for 2 hours. The solution is concen-trated by evaporation aad subjected to conventional work-up to give ethyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinylmethyl)-4-aminopiperidine-4-acetate, FAB

~= ~s ~i f,; V ..i.
'y 387.
b) By analogy with Example 8, ethyl 1-(3-(4-amidino phenyl)-2-oxo-5-oxazolidinylmethyl)-4-amino piperidine-4-acetate, FAB 404, is obtained there from.
c) By analogy with Example 16, 1-(3-(4-amidinophenyl)-2-oxo-5-oxazolidinylmethyl)-4-aminopiperidine-4-acetic acid, FAB 376, is obtained therefrom by hydrolysis.
Example 18 a) By analogy with Example 17a) , from ethyl 1- (3- (4-cyanophenyl)-2-oxo-5-oxazolidinylmethyl)-4-methane-sulfonyloxypiperidine-4-carboxylate (obtainablefrom the 4-hydroxy compound (see Example 13) with methanesulfonyl chloride/pyridine) with NH3, ethyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinylmethyl)-4-aminopiperidine-4-carboxylate, FAB 373, is obtained.
b) By analogy with Example 8, ethyl 1-(3-(4-amidino phenyl)-2-oxo-5-oxazolidinylmethyl)-4-amino piperidine-4-carboxylate, ~ FAB 390, is obtained therefrom.
c) By analogy with Example 16, 1-(3-(4-amidinophenyl) 2-oxo-5-oxazolidinylmethyl)-4-aminopiperidine-4 carboxylic acid, FAB 362, is obtained therefrom by hydrolysis.
Example 19 A solution of 1 g of benzyl 3- (4- (3- (4-hydroxy-amidinophenyl)-2-oxo-5R- or -5S-oxazolidinyl-methyl)-1-piperazinyl)propionate (see Example 15) in 30 ml of acetic acid. with the addition of 1 ml of acetic anhydride, is hydrogenated over 0.2 g of 10 % Pd-C at 20° aad 1 bar, until the calculated quantity of hydrogen hae been taken up. The mixture is filtered and subjected to conventional work-up to give:
3-(4-(3-(4-Amidinophenyl)-2-oxo-5R-oxazolidinyl-methyl)-1-piperazinyl)propionic acid, acetate, m.p. 200-220° (decomp.), [alD~ +9° (c = 0.5, DMSO) or ~:. rf cJ ? _i.

3-(4-(3-(4-Amidinophenyl)-2-oxo-5S-oxazolidinyl-methyl)-1-piperazinyl)propionic acid, acetate, m.p. 200-220° (decomp.), [a]D° -8° (c = 0.5, DMSO).
The following examples relate to pharmaceutical formulations.
E~camt~le A: Tablets A mixture of 1 kg of active compound of the Formula I, 4 kg of lactose, 1.2 kg of corn starch, 200 g of talc and 100 g of magnesium stearate is compressed in 10. the customary manner to form tablets such that each tablet contains 100 mg of active compound.
Example B: Coated tablets Tablets are moulded in analogy with Example A, which tablets are then coated, in a customary manger, with a coating consisting of sucrose, corn starch, talc, tragacanth and colorant.
Examale C: Capsules Hard gelatin capsules are filled, in a customary manner, with 500 g of active compound of the formula I
such that each capsule contains 500 mg of active com pound.
Example D: Injection vials A solution of 100 g of active compound of the formula I in 4 1 of doubly-distilled water is adjusted to pH 6.5 with 2 N hydrochloric acid and filtered to reader it sterile, and then used to fill injection vials. The vial contents are lyophilized, and the vials then sealed, under sterile conditions. Each injection vial contains 50 mg of active compound.
E~camflle 8: Suppositories A mixture of 50 g of active compound of the formula I together with 10 g of soybean lecithin and 140 g of cacao butter is melted and then poured into moulds and allowed to cool. Each suppository contains 250 mg of active compound.

Claims

1. ~A compound of formula I
in which X is O, S, NH or NA, Y is an aziridino, azetidino, pyrrolidino, piperidino, 1-oxa-8-azaspiro[4.5]dec-8-yl, hexahydroazepino or 4-R4-piperazino radical which is unsubstituted or substituted once by R2, which can additionally be substituted by an OZ, SZ or N(Z)2 group and/or by carbonyl oxygen, Z is in each case H, A, phenyl-C k H2k or aryl having 1-11 C atoms, R1 is a phenyl radical which is substituted once by CN, H2N-CH2-, (A)2N-CH2-, H2N-C(=NH)-, H2N-C(=NH)-NH-, H2N-C(=NH)-NH-CH2-, HO-NH-C(=NH)- or HO-NH-C(=NH)-NH, R2 is -C m H2m-COOR3 or -C n H2n-O-C p H2p-COOR3, R3 is H, A or benzyl, R4 is H, A, benzyl or -C m H2m-COOR3, A is in each case alkyl having 1-6 C atoms, k and m are in each case 0, 1, 2 or 3, n is 0, 1 or 2, and p is 1, 2 or 3, or a salt thereof.

2. ~1-(3-(4-Amidinophenyl)-2-oxo-5-oxazolidinyl-methyl)piperidine-4-carboxylic acid.

3. ~A process for preparing a compound of the formula I according to claim 1, or a salt thereof, wherein:
(a) a compound of the formula I is liberated from one of its functional derivatives by treating with a solvolysing or hydrogenolysing agent;
(b) a compound of the formula II
in which E is Cl, Br, I, or a reactive esterified OH group, and R1 and X have the abovementioned meanings, is reacted with an amino compound of the formula III
H-Y ~~~~~III
in which Y has the abovementioned meaning;
(c) a compound of the formula IV
R1-NH-CH2-CH(XH)-CH2-Y ~~~IV
in which R1, X and Y have the abovementioned meanings, or one of its reactive derivatives, is reacted with a reactive derivative of carbonic acid; or (d) in order to prepare a guanidino compound of the formula I (R1 = phenyl radical substituted once by H2N-C(=NH)-NH), an amino compound corresponding to the formula I, which, however, contains an aminophenyl group in place of the radical R1, is treated with an amidinating agent; and optionally one or more of:
(i) in the compound of the formula I, one or both radicals R1 and Y is transformed into (an)other radical(s) R1 and Y; and (ii) the compound of the formula I is converted into a salt thereof by treatment with an acid or a base.

4. A process for preparing a pharmaceutical formulation, wherein a compound of the formula I as claimed in claim 1 or one of its physiologically harmless salts is brought into a suitable dosage form together with at least one solid, liquid or semi-liquid excipient or auxiliary agent.

5. A pharmaceutical formulation, comprising one or more compound of the formula I as claimed in claim 1 or a physiologically harmless salt thereof and a pharmaceutically acceptable carrier, excipient, auxiliary agent or diluent.

6. Use of a compound of formula I as claimed in claim 1, or a physiologically harmless salt thereof in preparing a medicament for inhibition of one or more fibrinogen receptor.

7. Use of a compound of formula I as claimed in claim 1, or a physiologically harmless salt thereof in control of one or more of thromboses, cardiac infarctions, stroke, osteoporosis, arteriosclerosis, inflammations and tumours, through inhibition of one or more fibrinogen receptor.