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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 524905생성일: 2026년 10월 25일

Thioacetic acid → HCID 90199365, 화합물

https://huagongshe.com/reaction/524905

반응식

참여 물질

역할이름HCID투입량
반응물Thioacetic acidHCID 10484—
반응물TriphenylphosphineHCID 11776—
반응물Diisopropyl azodicarboxylateHCID 5363146—
반응물HCID 86720960HCID 86720960—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물HCID 90199365HCID 90199365—

반응 단계

isopropyl (NE)-N-isopropoxycarbonyliminocarbamate (723.1 mg, 3.576 mmol) was added dropwise to a solution of 1-(3-chloro-5-fluoro-4-pyridyl)piperidin-4-ol (750 mg, 3.251 mmol) and Triphenylphosphine (937.9 mg, 828.5 μL, 3.576 mmol) in THF at −20° C. After stirring for 15 mins, ethanethioic S-acid (272.2 mg, 255.6 μL, 3.576 mmol) was added, the mixture was allowed to warm to room temperature and was stirred for a further 30 minutes. The mixture was then diluted with ethylacetate (30 ml), washed twice with water (20 ml) and with brine. The organic layer was dried with MgSO4 and concentrated in vacuo to a yellow solid that was purified by column chromatography eluting with 5/95 ether/pet ether to elute side products and then 10/90 ether/pet ether. The relevant fractions were combined and concentrated in vacuo to afford S-(1-(3-chloro-5-fluoropyridin-4-yl)piperidin-4-yl) ethanethioate as a green solid. MS (ES+) 289.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09340546B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-084a3e97478741ebbc630aeacb88ad29
출처 메모uspto-grants-2016_05