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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | 3-Chloro-1-propanol | HCID 12313 | — |
| 반응물 | Sodium Methoxide | HCID 10942334 | — |
| 반응물 | N-[4-(4-Piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-2-(acetylthio)acetamide | HCID 86750622 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | N-[4-(4-piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-2-(3-hydroxypropylthio)acetamide | HCID 67726286 | 81% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05616579 |
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| 출처 데이터셋 | uspto-grants-1997_04 |
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| ORD ID | ord-75936c190cbc4c32ab18f956ab1df720 |
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| 출처 메모 | uspto-grants-1997_04 |
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