FIELD: organic chemistry, heterocyclic compounds. SUBSTANCE: invention relates to derivatives of pyrrolo[2,3-d] pyrimidines of the formula (I) where B - group ; R1 - H, alkyl possibly substituted with hydroxy-group, alkoxyl, N-((C1-2-alkyl)- -((C1-4-alkyl)-group; R2 - alkyl, C3-8-cycloalkyl, ((C1-6-alkylene)-C3-8-cycloalkyl, C1-10-alkylenephenyl optionally substituted with alkyl in phenyl ring; R3, R4 and R6 - hydrogen or alkyl; R5 - phenyl substituted with 1-3 substituents taken from fluorine, chlorine, bromine, alkyl, alkoxy, trifluoromethyl or a single OH, J, NH2, NH-alkyl, COO-alkyl, formyl where alkyl can be substituted with fluorine, chlorine atoms, hydroxy-, alkoxy-group or to have a single double bond; R11 - H, F, chlorine, CO-((C1-2-alkyl), COO-((C1-2-alkyl); R12 - H or C1-4-alkyl, or their pharmaceutically acceptable salts showing antagonistic activity with respect to corticotropin releasing factor. EFFECT: improved method of synthesis, enhanced activity of compounds. 13 cl, 22 tbl, 38 ex
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Authors
Dates
1998-12-27—Published
1993-11-12—Filed