HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 6-Acetylamino-1-(2-chlorobenzyl)-2-n-propylbenzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(2-Chlorobenzyl)-2-propyl-1H-benzo[d]imidazol-6-amine | HCID 12042348 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Acetylamino-1-(2-chlorobenzyl)-2-n-propylbenzimidazole | HCID 22620334 | 83.6% |
Reaction Steps
Acetic anhydride (62 mg) was added to a solution of 150 mg of 6-amino-1-(2-chlorobenzyl)-2-n-propylbenzimidazole and 61 mg of triethylamine in 3 ml of methylene chloride at room temperature, and the mixture was stirred for 1 hour. The reaction mixture was washed with water, and was then dried. The solvent was distilled off under reduced pressure. The residue was crystallized with ether to give 143 mg of 6-acetylamino-1-(2-chlorobenzyl)-2-n-propylbenzimidazole (89).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06352985B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-9460f47d03324717ab734aaa7167f101 |
| Source note | uspto-grants-2002_03 |