C - Chemistry – Metallurgy – 07 – D
Patent
C - Chemistry, Metallurgy
07
D
C07D 403/06 (2006.01) A61K 31/395 (2006.01) C07D 401/14 (2006.01) C07D 403/14 (2006.01) C07D 405/14 (2006.01) C07D 409/14 (2006.01) C07D 413/14 (2006.01) C07D 417/14 (2006.01) C07F 1/00 (2006.01) C07F 3/00 (2006.01) C07F 5/02 (2006.01) C07F 7/10 (2006.01) C07F 7/22 (2006.01)
Patent
CA 2117498
A compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R is phenyl, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, furyl or thienyl, all of which may be optionally substitued by halo, C1-C4 alkyl, C1-C4 alkoxy or a group of the formula: -X-R2; R1 is H, C1-C6 alkyl, C3-C7 cycloalkyl, C5-C7 cycloalkenyl, C3-C6 alkenyl or C3-C6 alkynyl, said alkyl group being optionally substituted by C3-C7 cycloalkyl, C3-C7 cycloalkyloxy, OH, C1-C6 alkoxy, CONR3R4, SO2NR3R4, COR5, SOR5, SO2R5, CO2R6, aryl, aryloxy, aryl(C1-C6)alkoxy or heteroaryl, said alkenyl group being optionally substituted by aryl and said cycloalkyl group being optionally substituted by OH; the cycloalkyl and cycloalkenyl groups of the foregoing groups being optionally linked to the N-atom by a C1-C2 alkylene moiety; R2 is COR7, CO2R7, SOR7, SO2R7, CONR3R4, SO2NR3R4, NHCOR7, NHCONR3R4, NHSO2R7, NHSO2NR3R4, OH or CN; R3 and R4 are either each independently selected from H, C3-C7 cycloalkyl and C1-C6 alkyl, said alkyl group being optionally substituted by C3-C7 cycloalkyl or aryl, or R3 and R4 taken together represent C3-C6 alkylene optionally interrupted by O, S(O)n, NH or N(C1-C6 alkyl); R5 is C1-C6 alkyl, C3-C7 cycloalkyl, C3-C7 cycloalkyl(C1-C6)alkylene, aryl(C1-C6)alkylene or aryl; R6 is C1-C6 alkyl, C3-C7 cycloalkyl or aryl(C1-C6)alkylene; R7 is C1-C6 alkyl; X is a direct link or C1-C7 alkylene; m is 1 or 2; and n is 0, 1 or 2; are selective 5-HT1-like receptor agonists useful in the treatment of migraine, cluster headache, chronic paroxysmal hemicrania and headache associated with vascular disorders.
Brown Alan Daniel
Dickinson Roger Peter
Wythes Martin James
Pfizer Research And Development Company N.v./s.a.
Smart & Biggar
LandOfFree
Indole derivatives as 5-ht1-like agonists does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Indole derivatives as 5-ht1-like agonists, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Indole derivatives as 5-ht1-like agonists will most certainly appreciate the feedback.
Profile ID: LFCA-PAI-O-1544212