Cyclopentanemethanol → 1-(3-Chloro-benzyl)-2-(2-cyclopentylmethoxy-pyridin-3-yl)-5,6-difluoro-1H-benzoimidazole
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:32]=[CH:33][CH:34]=1)[CH2:5][N:6]1[C:10]2[CH:11]=[C:12]([F:16])[C:13]([F:15])=[CH:14][C:9]=2[N:8]=[C:7]1[C:17]1[C:18]([O:23][CH2:24][C:25]2[CH:30]=C[CH:28]=[CH:27][C:26]=2Cl)=[N:19][CH:20]=[CH:21][CH:22]=1.C1(CO)CCCC1>>[Cl:1][C:2]1[CH:3]=[C:4]([CH:32]=[CH:33][CH:34]=1)[CH2:5][N:6]1[C:10]2[CH:11]=[C:12]([F:16])[C:13]([F:15])=[CH:14][C:9]=2[N:8]=[C:7]1[C:17]1[C:18]([O:23][CH2:24][CH:25]2[CH2:26][CH2:27][CH2:28][CH2:30]2)=[N:19][CH:20]=[CH:21][CH:22]=1Participants
3
Procedure
The title compound was prepared in analogy to Example 1, from 1-(3-chloro-benzyl)-2-(2-chloro-pyridin-3-yl)-5,6-difluoro-1H-benzoimidazole (Example 11, intermediate) and cyclopentyl-methanol (CAS Reg. No. 3637-61-4). Colorless powder (52%). MS (Turbo Spray): m/z=454.1 (M+H).
Sources & evidence
- ORD record
- ord-e78033c4e31a4e8b95bdc557ba915e1e
- Source dataset
- uspto-grants-2012_11
- Patent number
- US08309581B2
Reaction notes
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