Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 237881생성일: 2026년 10월 27일
Ethyl chloroformate → (S)-2-(4-Cyclohexyl-phenoxymethyl)-5-ethoxy-2,3-dihydro-oxazolo[3,2-a]pyrimidin-7-one
https://huagongshe.com/reaction/237881
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl chloroformate | HCID 10928 | — |
| 반응물 | 4-Cyclohexylphenol | HCID 14327 | — |
| 반응물 | Ether, ethyl ethynyl | HCID 61239 | — |
| 반응물 | (-)-Epichlorohydrin | HCID 2734062 | — |
| 반응물 | (S)-5-(4-cyclohexyl-phenoxymethyl)-4,5-dihydro-oxazol-2-ylamine | HCID 66875140 | — |
| 반응물 | 3-Ethoxy-propynoic acid ethyl ester | HCID 86640241 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | (S)-2-(4-Cyclohexyl-phenoxymethyl)-5-ethoxy-2,3-dihydro-oxazolo[3,2-a]pyrimidin-7-one | HCID 68524745 | 41% |
반응 단계
To a solution of (S)-5-(4-cyclohexyl-phenoxymethyl)-4,5-dihydro-oxazol-2-yl-amine (0.98 g, 3.58 mmol) (prepared in accordance with the procedures described in Steps 1 and 2 of Example 1 starting from R-epichlorohydrin and 4-cyclohexylphenol) in 50 ml of ethanol was added freshly prepared 3-ethoxy-propynoic acid ethyl ester (0.65 g, 4.58 mmol), prepared from 6 ml of 50% ethoxyacetylene and 3.3 ml of ethyl chloroformate (Synthesis, 1989, 123-4). The mixture was stirred for 15 min at room temperature after which it was stirred at 60-65 degrees C. for 6h. The reaction mixture was concentrated to a yellow solid, dissolved in dichloromethane and flash chromatographed on silica gel eluting with dichloromethane/ammonia/methanol to provide 0.544 g of the title compound as a white solid. [α]D25 −1.00 (c 0.5, CHCl3).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08642603B2 |
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| 출처 데이터셋 | uspto-grants-2014_02 |
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| ORD ID | ord-564a3ea891ee47988b432a70fe7213e2 |
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| 출처 메모 | uspto-grants-2014_02 |
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