HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorobenzimidazole → N-(Benzimidazol-2-yl)-2,2-bis(4-chlorophenyl)ethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorobenzimidazole | HCID 78572 | — |
| Reactant | 2,2-Bis(4-chlorophenyl)ethanamine | HCID 13110442 | — |
| Product | N-(Benzimidazol-2-yl)-2,2-bis(4-chlorophenyl)ethylamine | HCID 11538181 | — |
Reaction Steps
The title compound was prepared from 2-chlorobenzimidazole and 2,2-bis(4-chlorophenyl)ethylamine (prepared by Procedure B from 2,2-bis(4-chloro-phenyl)acetaldehyde) by Procedure A (20 min at 170° C.). The product was isolated by preparative LCMS to give the title compound as the free base (white solid, mp 189-190° C.). MS(ES+) m/z 382 ([M+1]+, 100). 1NMR (DMSO-d6) δ 3.91 (m, 2H), 4.47 (t, 1H), 6.52 (m, 1H), 6.81-6.90 (m, 2H), 7.06-7.18 (m, 2H), 7.33-7.36 (m, 8H), 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-cb90506abb62481699de42a7252ee56c |
| Source note | uspto-grants-2010_06 |