1-(4-Chlorophenyl)-1H-imidazole → 6-[3-(4-Chloro-phenyl)-3H-imidazol-4-yl]-1-(4-fluoro-phenyl)-1H-benzoimidazole

HRID 2202481Notes

Reaction equation

HRID 2202481 reaction equation
Br[C:2]1[CH:3]=[CH:4][C:5]2[N:9]=[CH:8][N:7]([C:10]3[CH:15]=[CH:14][C:13]([F:16])=[CH:12][CH:11]=3)[C:6]=2[CH:17]=1.[Cl:18][C:19]1[CH:24]=[CH:23][C:22]([N:25]2[CH:29]=[CH:28][N:27]=[CH:26]2)=[CH:21][CH:20]=1>>[Cl:18][C:19]1[CH:20]=[CH:21][C:22]([N:25]2[C:29]([C:2]3[CH:3]=[CH:4][C:5]4[N:9]=[CH:8][N:7]([C:10]5[CH:15]=[CH:14][C:13]([F:16])=[CH:12][CH:11]=5)[C:6]=4[CH:17]=3)=[CH:28][N:27]=[CH:26]2)=[CH:23][CH:24]=1

Participants

3

Procedure

The title compound, off-white solid (20 mg, 15%), MS (ISP) m/z=389.5 [(M+H)+], mp 254° C., was prepared in accordance with the general method of example 28 from 6-bromo-1-(4-fluoro-phenyl)-1H-benzo[d]imidazole (intermediate G) (204 mg, 0.7 mmol) and commercially available 1-(4-chloro-phenyl)-1H-imidazole (62.5 mg, 0.35 mmol).

Sources & evidence

ORD record
ord-c809eb996dbe4c8d9b9805bbd97a0a57
Source dataset
uspto-grants-2016_06
Patent number
US09365550B2

Reaction notes

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