HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → 1-(2-(Piperazin-1-yl)pyrimidin-5-yl)ethanone hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2,2,2-Trifluoroethyl Acetate | HCID 136256 | — |
| Reactant | Tert-butyl 4-(5-acetylpyrimidin-2-yl)piperazine-1-carboxylate | HCID 118023389 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2-(Piperazin-1-yl)pyrimidin-5-yl)ethanone hydrochloride | HCID 118022442 | 100% |
Reaction Steps
To a solution of tert-butyl 4-(5-acetylpyrimidin-2-yl)piperazine-1-carboxylate (3 g, 9.8 mmol) in dichloromethane (30 mL) was added trifluoroethyl acetate (15 mL), and the mixture was stirred at RT for 30 min. LCMS showed the reaction was completed. The reaction mixture was neutralized with sodium carbonate solution and extracted with dichloromethane. The organic layer was dried over sodium sulfate, filtered and concentrated to afford the title compound as a light yellow solid (2 g, 100%), which was directly used in the next step without further purification. MS (ES+) C10H14N4O requires: 206. found: 207 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09200002B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-937750007d704c6eb644c13b6cb9c520 |
| Source note | uspto-grants-2015_12 |