HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorobenzimidazole → N-(Benzimidazol-2-yl)-4,4'-dichlorobenzhydrylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorobenzimidazole | HCID 78572 | — |
| Reactant | 4-Chloro-alpha-(4-chlorophenyl)benzenemethanamine | HCID 11196067 | — |
| Product | N-(Benzimidazol-2-yl)-4,4'-dichlorobenzhydrylamine | HCID 11603090 | — |
Reaction Steps
The title compound was prepared from 2-chlorobenzimidazole and 4,4′-dichlorobenzhydrylamine (prepared by Procedure B from 4,4′-dichlorobenzophenone) by Procedure A. The product was isolated by preparative LCMS to give the title compound as the free base (white solid, mp 176-180° C.). MS(ES+) m/z 368 ([M+1]+, 100). 1NMR (DMSO-d6) δ6.19 (d, 1H), 6.82-6.90 (m, 2H), 7.10-7.16 (m, 2H), 7.40 (s, 8H), 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-21faa14c17de4db8a6d3eec40b762b9a |
| Source note | uspto-grants-2010_06 |