HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorobenzimidazole → N-(Benzimidazol-2-yl)-4-chlorobenzhydrylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorobenzimidazole | HCID 78572 | — |
| Reactant | 4-Chlorobenzhydrylamine hydrochloride | HCID 16219096 | — |
| Product | N-(Benzimidazol-2-yl)-4-chlorobenzhydrylamine | HCID 11660016 | — |
Reaction Steps
The title compound was prepared from 2-chlorobenzimidazole and 4-chlorobenzhydrylamine HCl by Procedure A. The product was isolated by preparative LCMS to give the title compound as the free base (white solid, mp 180-184° C.). MS(ES+)m/z 334 ([M+1]+, 100). 1NMR (DMSO-d6) δ 6.18 (d, 1H), 6.80-6.90 (m, 2H), 7.08-7.14 (m, 2H), 7.20-7.40 (m, 9H), 7.66 (d, 1 H), 10.6 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07737167B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-fb47033a3ca14588b0ba2abc8b5a6d00 |
| Source note | uspto-grants-2010_06 |