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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1526870생성일: 2026년 10월 26일

(1R,3S)-3-[(tert-butoxycarbonyl)amino]cyclopentyl methanesulfonate → methyl 4-[4-([[(1S,3S)-3-[[(tert-butoxy)carbonyl]amino]cyclopentyl]sulfanyl]methyl)-5-methyl-1,3-oxazol-2-yl]benzoate

https://huagongshe.com/reaction/1526870

반응식

참여 물질

역할이름HCID투입량
반응물(1R,3S)-3-[(tert-butoxycarbonyl)amino]cyclopentyl methanesulfonateHCID 86608906—
반응물Methyl 4-[5-methyl-4-(sulfanylmethyl)-1,3-oxazol-2-yl]benzoateHCID 86709134—
용매DimethylformamideHCID 6228—
생성물methyl 4-[4-([[(1S,3S)-3-[[(tert-butoxy)carbonyl]amino]cyclopentyl]sulfanyl]methyl)-5-methyl-1,3-oxazol-2-yl]benzoateHCID 8670913588%

반응 단계

To a solution of methyl 4-[5-methyl-4-(sulfanylmethyl)-1,3-oxazol-2-yl]benzoate (920 mg, 3.49 mmol, 1.00 equiv) in N,N-dimethylformamide (20 mL) maintained under an inert atmosphere of nitrogen was added cescium carnonate (2.3 g). The mixture was stirred for 20 min then tert-butyl N-[(1S,3R)-3-(methanesulfonyloxy)cyclopentyl]carbamate (1.0 g, 3.58 mmol, 1.02 equiv) was added. The resulting solution was stirred at 35° C. for 50 min then the product was precipitated by the addition of 50 mL water. The precipitate was collected by filtration, washed with water and then dried under vacuum to give 1.37 g (88%) of methyl 4-[4-([[(1S,3S)-3-[[(tert-butoxy)carbonyl]amino]cyclopentyl]sulfanyl]methyl)-5-methyl-1,3-oxazol-2-yl]benzoate as a white solid. LC-MS: (ES, m/z): 447 [M+H]+, 391, 271, 230, 115.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09085570B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-874ab50e7dbe41e997300154572b1661
출처 메모uspto-grants-2015_07