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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52110생성일: 2026년 10월 27일

Water → N-[4-(4-piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-2-(3-hydroxypropylthio)acetamide

https://huagongshe.com/reaction/52110

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물3-Chloro-1-propanolHCID 12313—
반응물Sodium MethoxideHCID 10942334—
반응물N-[4-(4-Piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-2-(acetylthio)acetamideHCID 86750622—
용매MethanolHCID 887—
생성물N-[4-(4-piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-2-(3-hydroxypropylthio)acetamideHCID 6772628681%

반응 단계

5 ml of a methanolic solution containing 0.26 g of a 28% w/v sodium methoxide solution were added, whilst ice-cooling, to a solution of 0.50 g of N-[4-(4-piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-2-(acetylthio)acetamide [prepared as described in step (b) above] in 5 ml of methanol, and the resulting solution was stirred for 20 minutes. At the end of this time, a solution of 0.11 ml of 3-chloro-1-propanol in 5 ml of methanol, was added, and the reaction mixture was heated under reflux for 5 hours. The solvent was then removed by distillation under reduced pressure. The residue thus obtained was mixed with water, and the aqueous mixture was extracted with ethyl acetate. The extract was concentrated by evaporation under reduced pressure, and the residue was purified by column chromatography through silica gel, using a 1:9 by volume mixture of methanol and methylene chloride as the eluent, to give 0.42 g (yield 81%) of the title compound as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616579
출처 데이터셋uspto-grants-1997_04
ORD IDord-75936c190cbc4c32ab18f956ab1df720
출처 메모uspto-grants-1997_04