Synthesis of substituted pyrazoline carboxamidine derivatives
This invention relates to organic chemistry, in particular to processes for the preparation of pyrazoline carboxamidine derivatives of formula (I), known as potent 5-HT6 antagonists. The invention also relates to novel intermediates of these compounds. wherein the symbols have the meanings given in the description.
1. A process for the preparation of a compound of formula (I):
or a tautomer, stereoisomer, or a pharmacologically acceptable salt thereof, wherein:
R 7 represents a monocyclic, or a fused-bicyclic aromatic or hetero-aromatic group, which groups are unsubstituted or substituted with one to five substituents which can be the same or different, selected from the group consisting of halogen, trifluoromethyl, trifluoromethoxy, cyano, C 1-3 -alkyl, C 1-3 -alkoxy, hydroxy, amino, acetyl, acetamido, trifluoroacetamido, —CONH 2 , —SO 2 NH 2 and —CO 2 H or R 7 represents a 2-aryl-ethenyl group or a 2-aryl-ethynyl group, or
R 7 represents a piperidinyl group unsubstituted or substituted with one to four fluoro atoms or a CF 3 group, or
R 7 represents a 2,3-dihydroindolyl group or a benzimidazol-2-one group
comprising the steps of:
(i) reacting 2,3-diaza-spiro[4.4]non-2-ene or 2,3-diaza-spiro[4.4]non-1-ene, or salts thereof with ethyl isothiocyanate, to yield 2,3-diazaspiro[4.4]non-3-ene-2-carbothioic acid ethylamide or its tautomer;
(ii) reacting the latter with iodomethane or methyl p-toluenesulfonate yielding N-ethyl-2,3-diaza-spiro[4.4]non-3-ene-2-carboximido-thioic acid methyl ester,
(iii) reacting the obtained N-ethyl-2,3-diaza-spiro[4.4]non-3-ene-2-carboximido-thioic acid methyl ester with a sulfonamide compound of formula R 7 SO 2 NH 2 , wherein R 7 has the meaning given above, to give a compound of formula (I):
(iv) isolating the compound of formula (I) from the reaction mixture.
2. A process as claimed in claim 1 , for the preparation of a compound of formula (I), wherein:
R 7 represents a monocyclic, or a fused-bicyclic aromatic or hetero-aromatic group, which groups are unsubstituted or substituted with one to five substituents which can be the same or different, selected from the group consisting of halogen, trifluoromethyl, trifluoromethoxy, cyano, C 1-3 -alkyl, C 1-3 -alkoxy, hydroxy, amino, acetyl, acetamido, trifluoroacetamido, —CONH 2 , —SO 2 NH 2 and —CO 2 H or R 7 represents a 2-aryl-ethenyl group or a 2-aryl-ethynyl group, or
R 7 represents a piperidinyl group, or
R 7 represents a 2,3-dihydroindolyl group or a benzimidazol-2-one group.
3. A process as claimed in claim 1 wherein R 7 represents a monocyclic, or a fused-bicyclic aromatic or hetero-aromatic group, which groups are unsubstituted or substituted with one or two substituents chosen from methyl, methoxy, fluoro, chloro, bromo, cyano, acetamido, trifluoroacetamido, trifluoromethyl, amino or hydroxy.
4. A process as claimed in claim 1 , for the preparation of a compound of formula
and tautomers and salt forms thereof,
comprising the steps of:
(i) reacting 2,3-diaza-spiro[4.4]non-2-ene or 2,3-diaza-spiro[4.4]non-1-ene, or salts thereof, with ethyl isothiocyanate, to yield 2,3-diazaspiro[4.4]non-3-ene-2-carbothioic acid ethylamide or its tautomer
(ii) reacting the latter with iodomethane or methyl p-toluenesulfonate yielding N-ethyl-2,3-diaza-spiro[4.4]non-3-ene-2-carboximido-thioic acid methyl ester,
(iii) reacting the latter, as free base or salt thereof, with 4-acetamidobenzenesulfonamide yielding N-(4-{[(2,3-diaza-spiro[4.4]non-3-en-2-yl)-ethylamino-methylene]-sulfamoyl}-phenyl)-acetamide
(iv) deprotecting the latter under acidic conditions, yielding 4-amino-N-[(2,3-diaza-spiro[4.4]non-3-en-2-yl)-ethylamino-methylene]-benzenesulfonamide
5. A process as claimed in claim 4 , wherein step (iii) consists of reacting N-ethyl-2,3-diaza-spiro[4.4]non-3-ene-2-carboximidothioic acid methyl ester with sulfanilamide yielding 4-amino-N-[(2,3-diaza-spiro[4.4]non-3-en-2-yl)-ethylamino-methylene]-benzenesulfonamide:
6. A compound selected from those of the formulae: