Antisecretory thiadiazole derivatives, processes for their manufacture and pharmaceutical compositions containing them

Claim 2

A thiadiazole derivative of the following formula I: ##STR10## wherein Y is an oxygen or sulphur atom, a direct bond or a methylene or sulphinyl radical; m is 0 to 4; n is 1 to 4; provided that when Y is a sulphur or oxygen atom or a sulphinyl radical m is 1 to 4, and when Y is an oxygen atom or a sulphinyl radical, n is 2 to 4; R 1 is a hydrogen atom or an alkyl radical of 1 to 10 carbon atoms; A is a 3,4-dioxocyclobuten-1,2-diyl radical or a radical of the formula C═Z in which Z is an oxygen or sulphur atom or Z is a radical of the formula NCN, NNO 2 , CHNO 2 , NCONH 2 , C(CN) 2 , NCOR 2 , NCO 2 R 2 , NSO 2 R 2 , or NR 3 in which R 2 is an alkyl radical of 1 to 6 carbon atoms or an aryl radical of 6 to 12 carbon atoms and R 3 is a hydrogen atom or an alkyl radical of 1 to 6 carbon atoms; and B is an alkoxy or alkylthio radical of 1 to 6 carbon atoms or a radical of the formula NR 4 R 5 in which R 4 and R 5 , which may be the same or different, are hydrogen atoms, alkyl radicals of 1 to 10 carbon atoms, alkenyl or alkynyl radicals of 3 to 6 carbon atoms in which the double or triple bond respectively is separated from the nitrogen atom of NR 4 R 5 by at least one carbon atom, (primary hydroxy)alkyl or (primary amino)alkyl radicals of 2 to 6 carbon atoms or cycloalkyl radicals of 3 to 6 carbon atoms, or R 4 and R 5 are joined to form, together with the nitrogen atom to which they are attached, a 5- or 6-membered saturated ring which optionally contains an additional oxygen atom or NH radical; and the pharmaceutically-acceptable acid-addition salts thereof.

Claim 3

The thiadiazole derivative as claimed in claim 1 in which R 1 is a hydrogen atom or a methyl radical, R 2 is a methyl or p-tolyl radical, R 3 is a hydrogen atom or a methyl radical, B is a methoxy, ethoxy or methylthio radical or a radical of the formula NR 4 R 5 in which R 4 and R 5 , which may be the same or different, are hydrogen atoms or methyl, ethyl, allyl, propargyl, 2-hydroxyethyl, 2-aminoethyl or cyclopropyl radicals, or R 4 and R 5 are joined to form, together with the nitrogen atom to which they are attached, a pyrrolidine, piperidine, piperazine or morpholine ring.

Claim 4

The thiadiazole derivative as claimed in claim 1 in which Y is a sulphur atom.

Claim 5

The thiadiazole derivative as claimed in claim 1 in which R 1 is a hydrogen atom.

Claim 6

The thiadiazole derivative as claimed in claim 1 in which B is a radical of the formula NR 4 R 5 in which R 5 is a hydrogen atom.

Claim 7

The thiadiazole derivative as claimed in claim 1 in which A is a 3,4-dioxocyclobuten-1,2-diyl radical or a radical of the formula C═Z in which Z is a sulphur atom or a radical of the formula NCN, NNO 2 , CHNO 2 , NCONH 2 or NSO 2 CH 3 .

Claim 8

The thiadiazole derivative as claimed in claim 1 in which m is 1, n is 2 and B is a radical of the formula NR 4 R 5 in which R 4 is a hydrogen atom or a methyl radical and R 5 is a hydrogen atom.

Claim 9

A thiadiazole derivative selected from the group consisting of 3-[2-(3-cyano-2-methylisothioureido)ethylthiomethyl]-5-guanidino-1,2,4-thiadiazole, 3-[2-(2-cyano-3-methylguanidino)ethylthio-methyl]-5-guanidino-1,2,4-thiadiazole, 3-[2-(2-cyano-3-ethylguanidino)ethylthiomethyl]-5-guanidino-1,2,4-thiadiazole, 3-[2-(2-cyano-3-[2-hydroxyethyl]guanidino)ethylthiomethyl]-5-guanidino-1,2,4-thiadiazole, 3-[2-(2-nitroguanidino)ethylthiomethyl]-5-guanidino-1,2,4-thiadiazole, 3-[2-(3-methylthioureido)ethylthiomethyl]-5-guanidino-1,2,4-thiadiazole, 1-(2-[(5-guanidino-1,2,4-thiadiazol-3-yl)methylthio]ethylamino)-1-methylamino-2-nitroethylene, 3-[2-(2-cyano-3-[2-aminoethyl]guanidino)ethylthiomethyl]-5-guanidino-1,2,4-thiadiazole or 3-[2-cyanoguanidino)ethylthiomethyl]-5-guanidino-1,2,4-thiadiazole and the pharmaceutically-acceptable acidaddition salts thereof.

Claim 10

A thiadiazole derivative selected from the group consisting of 3-[2-(3-cyano-2-methylisothioureido)ethylthiomethyl]-5-guanidino-1,2,4-thiadiazole, 3-[2-(2-cyano-3-methylguanidino)ethylthio-methyl]-5-guanidino-1,2,4-thiadiazole, 3-[2-(2-cyano-3-ethylguanidino)ethylthiomethyl]-5-guanidino-1,2,4-thiadiazole, 3-[2-(2-cyano-3-[2-hydroxyethyl]guanidino)ethylthiomethyl]-5-guanidino-1,2,4-thiadiazole, 3-[2-(2-nitroguanidino)ethylthiomethyl]-5-guanidino-1,2,4-thiadiazole, 3-[2-(3-methylthioureido)ethylthiomethyl]-5-guanidino-1,2,4-thiadiazole, 1-(2-[(5-guanidino-1,2,4-thiadiazol-3-yl)methylthio]ethylamino)-1-methylamino-2-nitroethylene, 3-[2-(2-cyano-3-[2-aminoethyl]guanidino)ethylthiomethyl]-5-guanidino-1,2,4-thiadiazole or 3-[2-cyanoguanidino)ethylthiomethyl]-5-guanidino-1,2,4-thiadiazole and the pharmaceutically-acceptable acidaddition salts thereof.

Claim 11

The thiadiazole derivative as claimed in claim 1, wherein said pharmaceutically-acceptable salt is selected from the group consisting of a hydrochloric, hydrobromic, phosphoric, sulphuric, citric or maleic acid salt.

Claim 12

A pharmaceutical composition for inhibiting acid secretion comprising an effective amount of the thiadiazole derivative as claimed in claim 1, 2, 3, 4, 5, 6, 7 or 8 in association with a non-toxic pharmaceutically-acceptable diluent or carrier.

Claim 13

A method of inhibiting gastric acid secretion in a living animal comprising administering to the animal a therapeutically effective amount of the pharmaceutical composition of claim 10.

Claim 14

A thiadiazole derivative of the following formula (III): ##STR11## wherein Y is an oxygen or sulphur atom, a direct bond or a methylene or sulphinyl radical; m is 0 to 4; n is 1 to 4; provided that when Y is a sulphur or oxygen atom or a sulphinyl radical, m is 1 to 4, and when Y is an oxygen atom or a sulphinyl radical, n is 2 to 4; and R 1 is a hydrogen atom or an alkyl radical of 1 to 10 carbon atoms.

Claim 15

A thiadiazole derivative of the following formula (III): ##STR11## wherein Y is an oxygen or sulphur atom, a direct bond or a methylene or sulphinyl radical; m is 0 to 4; n is 1 to 4; provided that when Y is a sulphur or oxygen atom or a sulphinyl radical, m is 1 to 4, and when Y is an oxygen atom or a sulphinyl radical, n is 2 to 4; and R 1 is a hydrogen atom or an alkyl radical of 1 to 10 carbon atoms.

Claim 16

The thiadiazole derivative of claim 12, wherein said derivative is 3-[(2-aminoethyl)thiomethyl]-5-guanidino-1,2,4-thiadiazole.

Claim 17

A process for the preparation of a thiadiazole of the following formula (XI): ##STR12## comprising the following steps: i. reacting a guanidine of the following formula (VII) with a thiadiazole of the following formula (VI): ##STR13## to form a guanidinothiadiazole of the following formula (XII): ##STR14## ii. reacting the guanidinothiadiazole of formula (XII) with an amine of the following formula (VIII): ##STR15## to form an aminothiadiazole of the following formula (XIII): ##STR16## iii. reacting the aminothiadiazole of formula (XIII) with R 6 -A-R 6 to form a compound of the following formula (XIV): ##STR17## iv. reacting the compound of formula (XIV) with B-H to form the thiadiazole product of formula (XI), wherein D is an oxygen or sulphur atom; m is 1 to 4; n is 1 to 4 when D is sulphur and n is 2 to 4 when D is oxygen; R 1 is a hydrogen atom or an alkyl radical of 1 to 10 carbon atoms; R 6 is a displaceable radical; A is a 3,4-dioxocyclobuten-1,2-diyl radical or a radical of the formula C═Z in which Z is a radical of the formula NCN, NNO 2 , CHNO 2 , NCONH 2 , C(CN) 2 , NCOR 2 , NCO 2 R 2 , NSO 2 R 2 or NR 3 in which R is an alkyl radical of 1 to 6 carbon atoms or an aryl radical of 6 to 12 carbon atoms and R 3 is a hydrogen atom or an alkyl radical of 1 to 6 carbon atoms; and B is an alkoxy or alkylthio radical of 1 to 6 carbon atoms or a radical of the formula NR 4 R 5 in which R 4 and R 5 , which may be the same or different, are hydrogen atoms, alkyl radicals of 1 to 10 carbon atoms, alkenyl or alkynyl radicals of 3 to 6 carbon atoms in which the double or triple bond respectively is separated from the nitrogen atom of NR 4 R 5 by at least one carbon atom, (primary hydroxy)alkyl or (primary amino)alkyl radicals of 2 to 6 carbon atoms or cycloalkyl radicals of 3 to 6 carbon atoms, or R 4 and R 5 are joined to form, together with the nitrogen atom to which they are attached, a 5- or 6-membered saturated ring which optionally contains an additional oxygen atom or NH radical.

Claim 18

A process for the preparation of a thiadiazole of the following formula (XI): ##STR12## comprising the following steps: i. reacting a guanidine of the following formula (VII) with a thiadiazole of the following formula (VI): ##STR13## to form a guanidinothiadiazole of the following formula (XII): ##STR14## ii. reacting the guanidinothiadiazole of formula (XII) with an amine of the following formula (VIII): ##STR15## to form an aminothiadiazole of the following formula (XIII): ##STR16## iii. reacting the aminothiadiazole of formula (XIII) with R 6 -A-R 6 to form a compound of the following formula (XIV): ##STR17## iv. reacting the compound of formula (XIV) with B-H to form the thiadiazole product of formula (XI), wherein D is an oxygen or sulphur atom; m is 1 to 4; n is 1 to 4 when D is sulphur and n is 2 to 4 when D is oxygen; R 1 is a hydrogen atom or an alkyl radical of 1 to 10 carbon atoms; R 6 is a displaceable radical; A is a 3,4-dioxocyclobuten-1,2-diyl radical or a radical of the formula C═Z in which Z is a radical of the formula NCN, NNO 2 , CHNO 2 , NCONH 2 , C(CN) 2 , NCOR 2 , NCO 2 R 2 , NSO 2 R 2 or NR 3 in which R is an alkyl radical of 1 to 6 carbon atoms or an aryl radical of 6 to 12 carbon atoms and R 3 is a hydrogen atom or an alkyl radical of 1 to 6 carbon atoms; and B is an alkoxy or alkylthio radical of 1 to 6 carbon atoms or a radical of the formula NR 4 R 5 in which R 4 and R 5 , which may be the same or different, are hydrogen atoms, alkyl radicals of 1 to 10 carbon atoms, alkenyl or alkynyl radicals of 3 to 6 carbon atoms in which the double or triple bond respectively is separated from the nitrogen atom of NR 4 R 5 by at least one carbon atom, (primary hydroxy)alkyl or (primary amino)alkyl radicals of 2 to 6 carbon atoms or cycloalkyl radicals of 3 to 6 carbon atoms, or R 4 and R 5 are joined to form, together with the nitrogen atom to which they are attached, a 5- or 6-membered saturated ring which optionally contains an additional oxygen atom or NH radical.

Claim 19

The process of claim 14 wherein R 1 is a hydrogen atom; m is 1; n is 2; D is a sulphur atom; A is C═Z in which Z is a radical of the formula NCN; and B is a radical of the formula NR 4 R 5 in which R 4 is a hydrogen atom and R 5 is a methyl radical.

Claim 20

A thiadiazole derivative as claimed in claim 1, wherein Y is a oxygen or sulphur atom.

Claim 21

A thiadiazole derivative as claimed in claim 1, wherein said derivative is 3-[2-(2-cyano-3-methylguanidino)ethylthiomethyl]-5-guanidino-1,2,4-thiadiazole.

Claim 22

A thiadiazole derivative as claimed in claim 1, wherein said derivative is a pharmaceutically-acceptable acid-addition salt of 3-[2-(2-cyano-3-methylguanidino)ethylthiomethyl]-5-guanidino-1,2,4-thiadiazole.

Claim 23

The thiadiazole derivative as claimed in claim 18, wherein said pharmaceutically-acceptable salt is selected from the group consisting of a hydrochloric, hydrobromic, phosphoric, sulphuric, citric or maleic acid salt.

Claim 24

A pharmaceutical composition for inhibiting acid secretion comprising an effective amount of the diadiazole derivative as claimed in claim 17 or 18 in association with a non-toxic pharmaceutically-acceptable diluent or carrier.