HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 1-[2-(5-Bromo-pyridin-3-yl)-pyrrolidin-1-yl]-ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 3-Bromo-5-(pyrrolidin-2-yl)pyridine | HCID 4403815 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[2-(5-Bromo-pyridin-3-yl)-pyrrolidin-1-yl]-ethanone | HCID 117667240 | 132% |
Reaction Steps
To a solution of 3-bromo-5-(2-pyrrolidinyl)pyridine (200 mg, 0.881 mmol) and pyridine (0.2 mL, 1.96 mmol) in DCM (1 mL) in a 8-mL vial is added acetic anhydride (0.093 mL, 0.969 mmol) dropwise. The mixture is stirred at room temperature for 2.5 h. The mixture is concentrated. The resulting crude product is purified by normal phase chromatography using 0-4.5% MeOH in DCM as the gradient to afford 1-[2-(5-bromo-pyridin-3-yl)-pyrrolidin-1-yl]-ethanone (313 mg, 83% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09181272B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-621fe542518d4dd4a7d446037a497fb3 |
| Source note | uspto-grants-2015_11 |