Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 237835생성일: 2026년 10월 25일
Ethyl chloroformate → (S)-2-(4-cyclohexyl-phenoxymethyl)-5-cyclopropyl-2,3-dihydro-oxazolo[3,2-a]pyrimidin-7-one
https://huagongshe.com/reaction/237835
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl chloroformate | HCID 10928 | — |
| 반응물 | Cyclopropylacetylene | HCID 138823 | — |
| 반응물 | Ethyl 3-cyclopropylprop-2-ynoate | HCID 639964 | — |
| 반응물 | (S)-5-(4-cyclohexyl-phenoxymethyl)-4,5-dihydro-oxazol-2-ylamine | HCID 66875140 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | (S)-2-(4-cyclohexyl-phenoxymethyl)-5-cyclopropyl-2,3-dihydro-oxazolo[3,2-a]pyrimidin-7-one | HCID 25071735 | 95.2% |
반응 단계
To a solution of (S)-5-(4-cyclohexyl-phenoxymethyl)-4,5-dihydro-oxazol-2-ylamine (0.5 g, 1.82 mmol), (see Example 28), in ethanol (5 mL) was added cyclopropyl-propynoic acid ethyl ester (0.377 g, 2.73 mmol) (prepared from ethynyl-cyclopropane and ethyl chloroformate in accordance with the procedures of G. Cai et al., Tetrahedron, 2006, 5697-5708). The reaction mixture was heated in a microwave oven at 170° C. for 30 min. The solvent was removed under vacuum, and the residue purified by flash column chromatography (silica gel, 2% 7N NH3 in MeOH/CH2Cl2) to afford 0.635 g of (S)-2-(4-cyclohexyl-phenoxymethyl)-5-cyclopropyl-2,3-dihydro-oxazolo[3,2-a]pyrimidin-7-one as a white solid. [α]D25 −13.40 (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-aecc2a065267432083b5bd97e1452303 |
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| 출처 메모 | uspto-grants-2014_02 |
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