Tri-substituted phenyl derivatives and processes for their...

C - Chemistry – Metallurgy – 07 – D

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C07D 213/30 (2006.01) A61K 31/09 (2006.01) A61K 31/33 (2006.01) C07C 43/235 (2006.01) C07C 43/247 (2006.01) C07C 69/94 (2006.01) C07C 205/35 (2006.01) C07C 255/54 (2006.01) C07D 207/333 (2006.01) C07D 213/61 (2006.01) C07D 215/14 (2006.01) C07D 217/16 (2006.01) C07D 217/22 (2006.01) C07D 237/08 (2006.01) C07D 239/24 (2006.01) C07D 239/26 (2006.01) C07D 239/28 (2006.01) C07D 239/38 (2006.01) C07D 239/42 (2006.01) C07D 307/42 (2006.01) C07D 333/16 (2006.01)

Patent

CA 2126072

Compounds are described in formula (1), wherein Y is a halogen atom or a group -OR1, where R1 is an optionally substituted alkyl group; R2 is an optionally substituted cycloalkyl or cycloalkenyl group; R3 is a monocyclic or bicyclic aryl group optionally containing one or more heteroatoms selected from oxygen, nitrogen or sulphur atoms or a group -N(R4)- where R4 is a hydrogen atom or an alkyl group; X is -O-, -S-, or -N(R5)-, where R5 is a hydrogen atom or an alkyl group; with the proviso that when X is -O- the R3 is not a 3-cyanamimo-6-pyridazinyl or a 3-chloro-6-pyridazinyl group; and the salts, solvates, hydrates and N- oxides thereof. The compounds are selective phosphodiesterase IV inhibitors and are useful for the prophylaxis or treatment of inflammatory diseases.

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