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HRID 2390991생성일: 2026년 10월 27일

Water → 4-[[(6-chloropyridin-3-yl)methyl](methyl)amino]furan-2(5H)-one

https://huagongshe.com/reaction/2390991

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium bisulfateHCID 516920—
반응물6-Chloro-N-methyl-3-pyridinemethanamineHCID 11094883—
반응물Methyl 4-hydroxy-2-oxo-2,5-dihydrofuran-3-carboxylateHCID 54677706—
용매DichloromethaneHCID 6344—
용매ButyronitrileHCID 8008—
생성물4-[[(6-chloropyridin-3-yl)methyl](methyl)amino]furan-2(5H)-oneHCID 11550459105%

반응 조건

온도115 °C

반응 단계

To a suspension of 18 g of 4-(methoxycarbonyl)-5-oxo-2,5-dihydrofuran-3-ol and 15 g of N-[(6-chloropyridin-3-yl)methyl]methylamine in 210 ml of butyronitrile are added, at room temperature, 16 g of potassium hydrogensulphate. The mixture is stirred at a temperature of 115° C. for 5 hours. Subsequently, the mixture is cooled to room temperature and admixed with 150 ml of water and 70 ml of dichloromethane. The organic phase is removed and the aqueous phase is extracted twice with 70 ml each time of methylene chloride. The combined organic phases are concentrated to dryness. 24 g of 4-[[(6-chloropyridin-3-yl)methyl](methyl)amino]furan-2(5H)-one are obtained in a purity of 88% (this corresponds to 92% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08273904B2
출처 데이터셋uspto-grants-2012_09
ORD IDord-e07d30df71024be7ad1cd76c8ef870c1
출처 메모uspto-grants-2012_09