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Pyridazine derivatives useful in therapy
专利权人:
Inhibitaxin Limited
发明人:
Gibson, Karl Richard,Owen, Dafydd Rhys
申请号:
ES12798852
公开号:
ES2648901T3
申请日:
2012.10.26
申请国别(地区):
ES
年份:
2018
代理人:
摘要:
Compound of formula I, ** Formula ** where: R 1 represents a cyclic group selected from phenyl, heteroaryl 1, heterocyclyl 1 and C 3-6 cycloalkyl; where each cyclic group is optionally substituted by 1 to 3 substituents selected from halo, C1-6 alkyl optionally substituted by 1-3 halogen atoms, phenyl, C1-6 alkoxy optionally substituted by 1-3 halogen atoms, cyano , heteroaryl1a and heterocyclyl1a; and where each cyclic group is optionally fused with a benzene ring or a 5- or 6-membered heteroaromatic or heterocyclic ring containing between 1 and 3 heteroatoms (selected from N, O and S); and when the group is replaced, the replacement can occur anywhere in the optionally fused ring system together; and where heterocyclyl1 and heterocyclyl1a can be substituted, additionally, by>; = O; X represents a bond or C1-6 alkylene (which can be straight or branched); R2 represents H or C1-6 alkyl; R3 represents H or C1-6 alkyl; Y represents CH (CH2CH2OH); R4 represents a cyclic group selected from phenyl, heteroaryl4, heterocyclyl4 and C3-6 cycloalkyl; where each cyclic group is optionally substituted by 1 to 3 substituents selected from halo, C1-6 alkyl optionally substituted by 1-3 halogen atoms, phenyl, C1-6 alkyl substituted by phenyl, C1-6 alkoxy optionally substituted by 1-3 halogen, cyano, heteroaryl4a and heterocyclyl4a atoms; and where each cyclic group is optionally fused with a benzene ring or a 5- or 6-membered heteroaromatic or heterocyclic ring containing between 1 and 3 heteroatoms (selected from N, O and S); and when the group is substituted, the substitution can occur anywhere in the optionally fused ring system together: and where heterocyclyl4 and heterocyclyl4a can, additionally, be substituted by>; = O; heteroaryl1, heteroaryl1a, heteroaryl4 and heteroaryl4a independently represent a 5- or 6-membered heteroaryl group containing between 1 and 3 heteroatoms (selected from N, O and S); and heterocyclyl1, heterocyclyl1a, heterocyclyl4 and heterocyclyl4a in
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