3-(Trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazole → 1-{4-[1-(1-pyrrolidinylcarbonyl)cyclopropyl]phenyl}-3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazole
反応式
I[C:2]1[CH:7]=[CH:6][C:5]([C:8]2([C:11]([N:13]3[CH2:17][CH2:16][CH2:15][CH2:14]3)=[O:12])[CH2:10][CH2:9]2)=[CH:4][CH:3]=1.[F:18][C:19]([F:30])([F:29])[C:20]1[C:28]2[CH2:27][CH2:26][CH2:25][CH2:24][C:23]=2[NH:22][N:21]=1>>[N:13]1([C:11]([C:8]2([C:5]3[CH:6]=[CH:7][C:2]([N:22]4[C:23]5[CH2:24][CH2:25][CH2:26][CH2:27][C:28]=5[C:20]([C:19]([F:18])([F:30])[F:29])=[N:21]4)=[CH:3][CH:4]=3)[CH2:10][CH2:9]2)=[O:12])[CH2:17][CH2:16][CH2:15][CH2:14]1参加物
3
実験手順
The title compound was prepared from 1-{[1-(4-iodophenyl)cyclopropyl]carbonyl}pyrrolidine and 3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazole using a similar procedure to that described for Example 19.
出典と根拠
- ORDレコード
- ord-b9fab832698a4b2dbe819eddf6ebf4b6
- 出典データセット
- uspto-grants-2010_01