HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 178474989, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178479260 | HCID 178479260 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178474989 | HCID 178474989 | 81% |
Reaction Steps
To a solution of 1-(trans-4-aminocyclohexane-1-ylcarbonyl)-4-(6-chloronaphthalene-2-sulfonyl)piperazine hydrochloride (50 mg) and triethylamine (30 mg) in dichloromethane (10 ml) was added acetic anhydride (50 mg), and the mixture was stirred at room temperature for 3 hours. The reaction solution was concentrated, and the residue was purified with silica gel column chromatography (ethyl acetate) to give colorless crystals of the title compound (41 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06359134B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-689c823ebf1c464eb6ae440fd04c6302 |
| Source note | uspto-grants-2002_03 |