HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorobenzimidazole → N-(Benzimidazol-2-yl)-4,4'-difluorobenzhydrylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorobenzimidazole | HCID 78572 | — |
| Reactant | 4-Fluoro-alpha-(4-fluorophenyl)benzenemethanamine | HCID 10955039 | — |
| Product | N-(Benzimidazol-2-yl)-4,4'-difluorobenzhydrylamine | HCID 11624170 | — |
Reaction Steps
The title compound was prepared from 2-chlorobenzimidazole and 4,4′-difluoro-benzhydrylamine (prepared by Procedure B from 4,4′-difluorobenzophenone) by Procedure A. The product was isolated by preparative LCMS to give the title compound as the free base (white solid, mp 241-243° C.). MS(ES+) m/z 336 ([M+1]+, 100). 1NMR (DMSO-d6) δ 6.20 (d, 1H), 6.80-6.91 (m, 2H), 7.09-7.20 (m, 6H), 7.38-7.43 (m, 4H), 7.69 (d, 1H), 10.6 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07737167B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-717e1b432dec4e4b906aaebcf91b3a05 |
| Source note | uspto-grants-2010_06 |