HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorobenzimidazole → HCID 11525259, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorobenzimidazole | HCID 78572 | — |
| Reactant | 3,4-Difluorobenzylamine | HCID 123572 | — |
| Reactant | 4-Chloro-3-(trifluoromethyl)benzyl bromide | HCID 2778114 | — |
| Product | HCID 11525259 | HCID 11525259 | — |
Reaction Steps
The title compound was prepared by Procedure B in two steps from 2-chloro-benzimidazole, 4-chloro-3-trifluoromethylbenzyl bromide and 3,4-difluorobenzylamine. The product was isolated by preparative LCMS to give the title compound as the free base (off-white solid, mp 158-161° C.). MS(ES+) m/z 452 ([M+1]+, 100). 1NMR (DMSO-d6) δ 4.55 (s, 2H), 5.36 (s, 2H), 6.87-6.98 (m, 2H), 7.13-7.37 (m, 6H), 7.50-7.55 (m, 1H), 7.68-7.71 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07842817B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-9de1c01e7ae544188c13fbec98d6de79 |
| Source note | uspto-grants-2010_11 |