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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 633703생성일: 2026년 10월 27일

Cesium carbonate → (8S)-2-chloro-9-(3-methyl-2-oxobutyl)-8-trifluoromethyl-6,7,8,9-tetrahydropyrimido[1,2-a]pyrimidin-4-one

https://huagongshe.com/reaction/633703

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물1-Bromo-3-methylbutan-2-oneHCID 10899037—
반응물(S)-8-chloro-2-(trifluoromethyl)-3,4-dihydro-1H-pyrimido[1,2-a]pyrimidin-6(2H)-oneHCID 136238740—
용매AcetonitrileHCID 6342—
생성물(8S)-2-chloro-9-(3-methyl-2-oxobutyl)-8-trifluoromethyl-6,7,8,9-tetrahydropyrimido[1,2-a]pyrimidin-4-oneHCID 11819445797.2%

반응 단계

A suspension of 170 mg (0.670 mmol) of (8S)-2-chloro-8-trifluoromethyl-6,7,8,9-tetrahydropyrimido[1,2-a]pyrimidin-4-one and 655.21 mg (2.01 mmol) of cesium carbonate in 10 mL of acetonitrile is stirred for 15 minutes at room temperature. 132.75 mg (0.804 mmol) of 1-bromo-3-methylbutan-2-one are then added. After stirring overnight at room temperature, the reaction mixture is evaporated and the residue is taken up in water and extracted with ethyl acetate. The organic phase is dried over magnesium sulfate and evaporated to dryness to give 220 mg of (8S)-2-chloro-9-(3-methyl-2-oxobutyl)-8-trifluoromethyl-6,7,8,9-tetrahydropyrimido[1,2-a]pyrimidin-4-one, corresponding to the following characteristics:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09321790B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-2be852f99f4743ef9e1c4208a1720b16
출처 메모uspto-grants-2016_04