HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 18465400, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | HCID 9821733 | HCID 9821733 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 18465400 | HCID 18465400 | 72.5% |
Reaction Steps
A mixture of 1-[1-(1-phenylcycloheptyl)-4-piperidyl]-1,3-dihydro-2H-1,3-benzimidazol-2-one (60 mg, 0.154 mmol, this was prepared as Example 17), pyridine (1 ml), acetic anhydride (44 μl, 0.462 mmol), and dimethylaminopyridine (6 mg, 0.0462 mmol) was stirred at room temperature for 1 h. After evaporation of the solvent, the residue was purified by preparative TLC (acetone/hexane:1/2) to give 48.2 mg (72.5%) of colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06423725B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-4fd322c6e74c4a4e8456415709e82f12 |
| Source note | uspto-grants-2002_07 |