HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorobenzimidazole → N-(Benzimidazol-2-yl)-2,2-bis(4-fluorophenyl)ethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorobenzimidazole | HCID 78572 | — |
| Reactant | 2,2-Bis(4-fluorophenyl)ethanamine | HCID 819761 | — |
| Product | N-(Benzimidazol-2-yl)-2,2-bis(4-fluorophenyl)ethylamine | HCID 11552019 | — |
Reaction Steps
The title compound was prepared from 2-chlorobenzimidazole and 2,2-bis(4-fluorophenyl)ethylamine (prepared by Procedure B from 2,2-bis(4-fluoro-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 155-157° C.). MS(ES+) m/z 350 ([M+1]+, 100) 1NMR (DMSO-d6) δ 3.90 (m, 2H), 4.46 (t, 1H), 6.50 (m, 1H), 6.80-6.90 (m, 2H), 7.07-7.18 (m, 6H), 7.35-7.42 (m, 4H), 10.5 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07737167B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-d4650308ee104cf59a72eb3ca6abb17b |
| Source note | uspto-grants-2010_06 |