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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 221372생성일: 2026년 10월 26일

tert-Butyl 4-sulfanylpiperidine-1-carboxylate → 4-(3-Pyridin-4-yl-[1,2,4]oxadiazol-5-ylmethylsulfanyl)piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/221372

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl 4-sulfanylpiperidine-1-carboxylateHCID 21906090—
반응물Potassium tert-butoxideHCID 23665647—
반응물Methanesulfonic acid 3-pyridin-4-yl-[1,2,4]oxadiazol-5-ylmethyl esterHCID 57954388—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물4-(3-Pyridin-4-yl-[1,2,4]oxadiazol-5-ylmethylsulfanyl)piperidine-1-carboxylic acid tert-butyl esterHCID 57954409—

반응 단계

t-BuOK (92 mg, 823 μmol) and methanesulfonic acid 3-pyridin-4-yl-[1,2,4]oxadiazol-5-ylmethyl ester (Preparation 12, 150 mg, 588 μmol) were added to a stirred solution of 4-mercaptopiperidine-1-carboxylic acid tert-butyl ester (191 mg, 881 mol) in anhydrous THF (10 ml). After 100 min, the reaction mixture was diluted with Et2O, before being washed with NaHCO3 and brine. The organic layer was dried (MgSO4), filtered, and concentrated, then the residue was purified by column chromatography (IH-EtOAc, 3:2) to afford the title compound: RT=3.77 min; m/z (ES+)=377.2 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207147B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-bad805c3d4a949ff81a3f21fa38fd134
출처 메모uspto-grants-2012_06