4-Fluoroaniline → N-(Benzimidazol-2-yl)-4-fluoroaniline
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]1[CH:18]=[CH:17][C:15]([NH2:16])=[CH:14][CH:13]=1>>[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][C:12]([F:11])=[CH:13][CH:14]=1Participants
3
Procedure
The title compound was prepared from 2-chlorobenzimidazole and 4-fluoroaniline by Procedure A. The product was isolated by filtration to give the title compound as a hydrochloride salt (solid, mp 215-216° C.). MS(ES+) m/z 228 ([M+1]+, 100).
Workup
- customThe product was isolated by filtration
Sources & evidence
- ORD record
- ord-7a9ba1d4483b4e619ae49de577a4378d
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07960561B2
Reaction notes
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