Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52076생성일: 2026년 10월 24일
Potassium Hydroxide → N-[4-(4-Piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-4-(2-pyrimidinylthio) butyramide
https://huagongshe.com/ko/reaction/52076
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | N-[4-(4-piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-4-chlorobutyramide | HCID 67726214 | — |
| 반응물 | HCID 178418793 | HCID 178418793 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | N-[4-(4-Piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-4-(2-pyrimidinylthio) butyramide | HCID 44211247 | 92.7% |
반응 단계
2.78 g of 2-mercaptopyrimidine were added to a solution of 1.95 g of 85% potassium hydroxide and 9.03 g of N-[4-(4-piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-4-chlorobutyramide (prepared as described in Preparation 2) in 140 ml of methanol, and the resulting mixture was heated under reflux for 15 hours. At the end of this time, the reaction mixture was cooled, and the solvent was removed by distillation under reduced pressure. The resulting residue was mixed with water, and the aqueous mixture was extracted with ethyl acetate. The extract was concentrated by evaporation under reduced pressure, and the concentrate was purified by column chromatography through silica gel, using a 9:1 by volume mixture of ethyl acetate and methanol as the eluent, to give 10.1 g (yield 92%) 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-6720e96c746444a589f225034fd47ddf |
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| 출처 메모 | uspto-grants-1997_04 |
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