Bromocyclopentane → 2-cyclopentyl-7-fluoro-3-(4-methoxyphenyl)-2H-indazole
Reaction equation
[F:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:10]=1[NH:9][N:8]=[C:7]2[C:11]1[CH:16]=[CH:15][C:14]([O:17][CH3:18])=[CH:13][CH:12]=1.[H-].[Na+].[CH:21]1(Br)[CH2:25][CH2:24][CH2:23][CH2:22]1>>[CH:21]1([N:8]2[C:7]([C:11]3[CH:16]=[CH:15][C:14]([O:17][CH3:18])=[CH:13][CH:12]=3)=[C:6]3[C:10]([C:2]([F:1])=[CH:3][CH:4]=[CH:5]3)=[N:9]2)[CH2:25][CH2:24][CH2:23][CH2:22]1Participants
4
Procedure
Prepared according to Method D step B from 7-fluoro-3-(4-methoxyphenyl)-1H-indazole (0.75 g, 3.1 mmol), sodium hydride (60% in oil, 0.124 g, 3.1 mmol) and cyclopentylbromide (0.36 mL, 3.3 mmol) to give the title compound (0.055 g) as a white solid.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-1f92ae07f73640bfa1edba0256b2ed63
- Source dataset
- uspto-grants-2007_07
- Patent number
- US07241791B2
Reaction notes
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