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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1498853Generated: November 3, 2026

Sodium Carbonate → 1-(2-(Piperazin-1-yl)pyrimidin-5-yl)ethanone hydrochloride

https://huagongshe.com/reaction/1498853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2,2,2-Trifluoroethyl AcetateHCID 136256—
ReactantTert-butyl 4-(5-acetylpyrimidin-2-yl)piperazine-1-carboxylateHCID 118023389—
SolventDichloromethaneHCID 6344—
Product1-(2-(Piperazin-1-yl)pyrimidin-5-yl)ethanone hydrochlorideHCID 118022442100%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09200002B2
Source datasetuspto-grants-2015_12
ORD IDord-937750007d704c6eb644c13b6cb9c520
Source noteuspto-grants-2015_12