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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | (1R,3S)-3-[(tert-butoxycarbonyl)amino]cyclopentyl methanesulfonate | HCID 86608906 | — |
| 반응물 | Methyl 4-[5-methyl-4-(sulfanylmethyl)-1,3-oxazol-2-yl]benzoate | HCID 86709134 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | methyl 4-[4-([[(1S,3S)-3-[[(tert-butoxy)carbonyl]amino]cyclopentyl]sulfanyl]methyl)-5-methyl-1,3-oxazol-2-yl]benzoate | HCID 86709135 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09085570B2 |
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| 출처 데이터셋 | uspto-grants-2015_07 |
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| ORD ID | ord-874ab50e7dbe41e997300154572b1661 |
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| 출처 메모 | uspto-grants-2015_07 |
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