HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-Difluoroaniline → HCID 11566903, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-Difluoroaniline | HCID 77469 | — |
| Reactant | 2-Chlorobenzimidazole | HCID 78572 | — |
| Reactant | 4-(Bromomethyl)-1,2-difluorobenzene | HCID 581436 | — |
| Solvent | Diethyl ether methanol | HCID 21864698 | — |
| Product | HCID 11566903 | HCID 11566903 | — |
Reaction Steps
The title compound was prepared by Procedure B in two steps from 2-chloro-benzimidazole, 3,4-difluorobenzyl bromide and 3,4-difluoroaniline. The product was isolated by filtration and recrystallization (MeOH/Et2O) to give the title compound as its hydrochloride salt (white solid, mp 236-238° C.). MS(ES+) m/z 372 ([M+1]+, 100). 1NMR (DMSO-d6) δ 5.61 (s, 2H), 7.19-7.30 (m, 3H), 7.36-7.61 (m, 6H), 7.83-7.91 (m, 1H), 11.0 (br s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07842817B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-71cfb61a15a54ea48757649904051042 |
| Source note | uspto-grants-2010_11 |