2-Chlorobenzimidazole → N-[3-Methoxy-5-(trifluoromethyl)phenyl]-1H-benzimidazol-2-amine
Reaction equation
Cl[C:2]1[NH:3][C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=1.[CH3:11][O:12][C:13]1[CH:14]=[C:15]([CH:17]=[C:18]([C:20]([F:23])([F:22])[F:21])[CH:19]=1)[NH2:16]>>[N:6]1[C:5]2[CH:7]=[CH:8][CH:9]=[CH:10][C:4]=2[NH:3][C:2]=1[NH:16][C:15]1[CH:17]=[C:18]([C:20]([F:22])([F:23])[F:21])[CH:19]=[C:13]([O:12][CH3:11])[CH:14]=1Participants
3
Procedure
The title compound was prepared from 2-chlorobenzimidazole and 3-methoxy-5-(trifluoromethyl)aniline by Procedure A. The product was isolated by filtration to give the title compound as a hydrochloride salt (white solid, mp 212-213° C.). MS(ES+) m/z 308 ([M+1]+, 100).
Workup
- customThe product was isolated by filtration
Sources & evidence
- ORD record
- ord-67ead7b83b164e1cb7315199b71649a0
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07960561B2
Reaction notes
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