HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 23369929, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 23369963 | HCID 23369963 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23369929 | HCID 23369929 | — |
Reaction Steps
To a solution of N-[4-(4-aminopiperidino)-2-(3,4-dichlorophenyl)butyl]-N-methylbenzamide (1.5 g) in dichloromethane (35 mL) was added triethylamine (0.60 mL) and acetic anhydride (0.41 mL), and the resulting solution was allowed to stir for 30 minutes. The mixture was diluted with dichloromethane and was washed (0.3N sodium hydroxide, water), dried, and evaporated. The material was dissolved in toluene and the resulting solution was evaporated to give the title compound (1.63 g) as a white solid; MS: m/z=476(M+1). Analysis for C25H31Cl2N3O2 ·0.2 C6H5CH3 : Calculated: C, 64.07; H, 6.63; N, 8.49; Found: C, 64.04; H, 6.59; N, 8.32.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05559132 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-32c17bf4ed9e45aeaeb53daedb269de8 |
| Source note | uspto-grants-1996_09 |