FIELD: chemistry.
SUBSTANCE: invention relates to a novel method for producing pan-CDK inhibitors (cyclin-dependent kinase) of general formula (I). Compounds of general formula (I) , where R4 is (C1-C6)-alkyl group or (C3-C7)-cycloalkyl ring, are obtained by connection of the previously obtained compounds (I-7-A) to (I-4-R) in the presence of benzenesulphonic acid as a catalyst, with resulting salts of benzenesulphonic acid (BSA) protected phenyl amine pyrimidine of formula (I-8-R-BSA) , with removal of protective groups in the salts of formula (I-8-R-BSA) by hydrogenation in the presence of palladium on active carbon in methanol and treatment with potassium carbonate in methanol to obtain compounds of formula (I) . Invention also relates to novel intermediate compounds of structural formulae (I-8-A-R-BSA) and (I-11-A-R-D-Tol-Tart). , .
EFFECT: method simplifies conditions for production of intermediate and end products, which allows its use on an industrial scale.
7 cl, 2 tbl
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RU2712233C2 |
Authors
Dates
2016-05-27—Published
2011-09-20—Filed