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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 879180생성일: 2026년 10월 26일

Potassium ethanethioate → (+/-)S-((1S,2R,4R,6S)-2-((tert-butoxycarbonyl)amino)-4-(3-((tert-butoxycarbonyl)amino)pyridin-4-yl)-6-methylcyclohexyl) ethanethioate

https://huagongshe.com/reaction/879180

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참여 물질

역할이름HCID투입량
반응물Potassium ethanethioateHCID 23670855—
반응물(1R,2R,4R,6S)-2-(tert-butoxycarbonylamino)-4-(3-(tert-butoxycarbonylamino)pyridin-4-yl)-6-methylcyclohexyl methanesulfonateHCID 86705223—
용매DimethylformamideHCID 6228—
생성물(+/-)S-((1S,2R,4R,6S)-2-((tert-butoxycarbonyl)amino)-4-(3-((tert-butoxycarbonyl)amino)pyridin-4-yl)-6-methylcyclohexyl) ethanethioateHCID 8670522487%

반응 조건

온도60 °C

반응 단계

To a solution of (+/−)-(1R,2R,4R,6S)-2-(tert-butoxycarbonylamino)-4-(3-(tert-butoxycarbonylamino)pyridin-4-yl)-6-methylcyclohexyl methanesulfonate (1.0 equiv.) in DMF (0.25 M) was added potassium thioacetate (6.0 equiv.). The mixture was stirred for 6 hours in a 60° C. bath under Ar. Upon cooling and the residue was partitioned between EtOAc and H2O. The organic layer was washed with H2O (3×), Na2CO3(sat.), NaCl(sat.), dried over MgSO4, filtered, concentrated and purified by ISCO SiO2 chromatography to yield (+/−)S-((1S,2R,4R,6S)-2-((tert-butoxycarbonyl)amino)-4-(3-((tert-butoxycarbonyl)amino)pyridin-4-yl)-6-methylcyclohexyl) ethanethioate in 87% yield. LC/MS (m/z)=480.3 (MH+), Rt=0.82 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08987457B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-6966415928bc430598124d6cd402a361
출처 메모uspto-grants-2015_03