FIELD: chemistry.
SUBSTANCE: invention relates to a novel pyrrolopyrimidine compound of general formula (I), a stereoisomer thereof or a pharmaceutically acceptable salt thereof. In general formula (I)
each of R1 and R2 is independently selected from a group consisting of H, halogen, cyano, C1-8alkyl, -NR7R8, -NH-C1-6alkylene-NR9R10, -NHCO-C1-6alkylene-NR9R10, -NH-C1-6alkylene-CO-NR9R10, -NHCO-C1-6alkylene-COO-C1-6alkyl, -NH-C3-6cycloalkylene-CO-NR9R10, -NH-C2-6alkenylene-CONR9R10, -NH-C1-6alkylene-cyano, -NHCO-NH-R11, -CONR12R13 and -CONH-C1-6alkylene-NR12R13, wherein C1-8alkyl is optionally substituted with hydroxyl, halogen, -NH2, -NH (C1-6alkyl), -N (C1-6alkyl)2, provided that R1 and R2 simultaneously are not H; each of R7 and R8 is independently selected from a group consisting of H, C1-6alkyl, C1-6alkylcarbonyl and C1-6alkylsulphonyl; or R7 and R8 together with atom N, to which they are bonded, form 5- or 6-member heterocyclyl, and said 5- or 6-member heterocyclyl contains atom N as a heteroatom and optionally substituted with oxo; each of R9 and R10 is independently selected from a group consisting of H, hydroxyl and C1-6alkyl; or R9 and R10 together with atom N, to which they are bonded, form 5- or 6-member heterocyclyl with 1-2 heteroatoms selected from N and O; R11 is selected from a group consisting of 5-member heteroaryl containing two N atoms and atom O as heteroatoms and optionally having substituent C1-4alkyl; each of R12 and R13 is independently selected from a group consisting of H and C1-6alkyl; R3 is selected from a group consisting of H and halogen; R4 is selected from a group consisting of cyano and -CONH2; and each of R5 and R6 is independently selected from a group consisting of H, hydroxyl and halogen.
EFFECT: compounds can be used for treating a tumour caused by Janus kinase activity, such a disease can be lymphoma, leukaemia.
19 cl, 7 tbl, 34 ex
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Authors
Dates
2019-09-25—Published
2015-12-15—Filed