HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 71522487, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 89500554 | HCID 89500554 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 71522487 | HCID 71522487 | 52.1% |
Reaction Steps
To a solution of 1-(2-{2-[3-(piperidin-2-yl)pyrrolidin-1-yl]ethyl}phenyl)piperidin-2-one a12-1 (25 mg, 0.070 mmol, 1 eq) in diethylether (2 ml) at 0° C. are added triethylamine and acetic anhydride (7 μl, 0.077 mmol, 1.1 eq). The mixture is stirred for 1 hour at room temperature. The solvent is removed under vacuum. The residue obtained is purified by basic reverse phase chromatography (gradient: acetonitrile/H2O/ammonium formate from 5% to 95% of acetonitrile in 8 minutes) to afford 14.5 mg of 1-(2-{2-[3-(1-acetylpiperidin-2-yl)pyrrolidin-1-yl]ethyl}phenyl)piperidin-2-one 72 as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09067930B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-a3902debe5bf410596e39ffbc8c00842 |
| Source note | uspto-grants-2015_06 |