Benzyl Bromide → 1-Benzyl-2-(2-chloro-pyridin-3-yl)-5,6-difluoro-1H-benzoimidazole

HRID 1875728Notes

Reaction equation

HRID 1875728 reaction equation
[Cl:1][C:2]1[C:7]([C:8]2[NH:12][C:11]3[CH:13]=[C:14]([F:18])[C:15]([F:17])=[CH:16][C:10]=3[N:9]=2)=[CH:6][CH:5]=[CH:4][N:3]=1.Br[CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>>[CH2:20]([N:12]1[C:11]2[CH:13]=[C:14]([F:18])[C:15]([F:17])=[CH:16][C:10]=2[N:9]=[C:8]1[C:7]1[C:2]([Cl:1])=[N:3][CH:4]=[CH:5][CH:6]=1)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1

Participants

3

Procedure

The title compound was prepared in analogy to Example 1, intermediate a, from 2-(2-chloro-pyridin-3-yl)-5,6-difluoro-1H-benzoimidazole and bromomethyl-benzene (CAS Reg. No. 100-39-0). Colorless solid (52%). MS (Turbo Spray): m/z=356.3 (M+H).

Sources & evidence

ORD record
ord-2de88540cdf44a35824de25ff5422075
Source dataset
uspto-grants-2012_11
Patent number
US08309581B2

Reaction notes

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