3-(Trifluoromethyl)aniline → N-(Benzimidazol-2-yl)-3-(trifluoromethyl)aniline
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.[F:11][C:12]([F:21])([F:20])[C:13]1[CH:14]=[C:15]([CH:17]=[CH:18][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]=[CH:18][CH:19]=[C:13]([C:12]([F:11])([F:20])[F:21])[CH:14]=1Participants
3
Procedure
The title compound was prepared from 2-chlorobenzimidazole and 3-(trifluoromethyl)aniline by Procedure A. The product was isolated by filtration and preparative LCMS to give the title compound as the free base (white solid, mp 160-162° C.). MS(ES+) m/z 278 ([M+1]+, 100).
Workup
- customThe product was isolated by filtration and preparative LCMS
Sources & evidence
- ORD record
- ord-5349ac32ae5c490081e1cca39dde2852
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07960561B2
Reaction notes
Loading…