Bromocyclopentane → 7-chloro-2-cyclopentyl-3-(4-methoxyphenyl)-2H-indazole

HRID 1294946Notes

Reaction equation

HRID 1294946 reaction equation
[Cl: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>>[Cl:1][C:2]1[C:10]2[C:6](=[C:7]([C:11]3[CH:16]=[CH:15][C:14]([O:17][CH3:18])=[CH:13][CH:12]=3)[N:8]([CH:21]3[CH2:25][CH2:24][CH2:23][CH2:22]3)[N:9]=2)[CH:5]=[CH:4][CH:3]=1

Participants

4

Procedure

Prepared according to Method D step B from 7-chloro-3-(4-methoxyphenyl)-1H-indazole (0.129 g, 0.5 mmol), sodium hydride (60% in oil, 0.024 g, 0.6 mmol) and cyclopentylbromide (0.107 mL, 1.0 mmol) to give the title compound (0.004 g).

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-f6d9497e5fb34859b48520703603437e
Source dataset
uspto-grants-2007_07
Patent number
US07241791B2

Reaction notes

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