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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 647511생성일: 2026년 10월 25일

Thiophenol → 4-Acetamido-1-(6-phenylthio-2-pyridyl)piperidine

https://huagongshe.com/reaction/647511

반응식

참여 물질

역할이름HCID투입량
반응물ThiophenolHCID 7969—
반응물Potassium CarbonateHCID 11430—
반응물2,6-DichloropyridineHCID 16989—
반응물N-Pyridin-4-ylacetamideHCID 21288—
반응물SodiumHCID 5360545—
반응물2-Chloro-6-(phenylthio)pyridineHCID 12760118—
용매SulfolaneHCID 31347—
생성물4-Acetamido-1-(6-phenylthio-2-pyridyl)piperidineHCID 1292661748.5%

반응 조건

온도150 °C

반응 단계

A mixture of 9.5 g of 2-chloro-6-(phenylthio) pyridine (b.p. 112° to 116° C./0.01 mm Hg, prepared by reaction of 2,6-dichloropyridine with the sodium salt of thiophenol), 7.8 g of potassium carbonate and 7.6 g of 4-acetamidopyridine in 75 ml of sulfolane is heated to 150° C. with stirring for 50 hours, then the sulfolane is concentrated to 1/5th of its volume, the mixture is poured in 100 ml of water and extraction is effected four times with 150 ml of diethyl ether. The organic phase is washed with water, dried over anhydrous sodium sulfate, concentrated to dryness and the residue is crystallised in 40 ml of ethyl acetate. 6.8 g of 4-acetamido-1-(6-phenylthio-2-pyridyl)piperidine are thus obtained; m.p. 110° to 112° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04409228
출처 데이터셋uspto-grants-1983_10
ORD IDord-617e70658e0147dbba88ec38debf31af
출처 메모uspto-grants-1983_10