Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 744808생성일: 2026년 10월 24일
Azide → 2-Oxazolidinone, 3-[(2S,4S)-4-azido-2-(1-methylethyl)-1-oxo-4-[(2S,4S)-tetrahydro-4-(1-methylethyl)-5-oxo-2-furanyl]butyl]-4-(phenylmethyl)-, (4S)-
https://huagongshe.com/ko/reaction/744808
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Azide | HCID 33558 | — |
| 반응물 | 1-Butanaminium, N,N,N-tributyl-, azide | HCID 5743232 | — |
| 반응물 | (4S)-3-[(2S,4R)-4-Bromo-2-(1-methylethyl)-1-oxo-4-[(2S,4S)-tetrahydro-4-(1-methylethyl)-5-oxo-2-furanyl]butyl]-4-(phenylmethyl)-2-oxazolidinone | HCID 54147056 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 2-Oxazolidinone, 3-[(2S,4S)-4-azido-2-(1-methylethyl)-1-oxo-4-[(2S,4S)-tetrahydro-4-(1-methylethyl)-5-oxo-2-furanyl]butyl]-4-(phenylmethyl)-, (4S)- | HCID 53385507 | — |
반응 단계
13.6 g of freshly dried tetrabutylammonium azide are added to a solution, stirred at room temperature, of 17.8 g of 3(S)-isopropyl-5(S)-{1(R)-bromo-4-methyl-3(S)-[(4(S)-benzyl-oxazolidin-2-on-3-yl)-carbonyl]-pentyl}-tetrahydrofuran-2-one in 180 ml of toluene, and a further 10 g of the azide are added in the course of 160 hours' stirring at room temperature. The reaction mixture is then partitioned between ethyl acetate and water (2x) and saturated sodium chloride solution (1x). The organic phases are combined, dried over sodium sulfate and concentrated. The title compound is obtained from the evaporation residue by means of FC (hexane/ethyl acetate=8:2) and crystallisation from diethyl ether/hexane: m.p.=102°-103° C.; Rf (hexane/ethyl acetate=8:2)=0.2; HPLC Rt =18.55 minutes; FAB-MS (M+H)+ =457.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05559111 |
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| 출처 데이터셋 | uspto-grants-1996_09 |
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| ORD ID | ord-4aaff9d4bd674caba17f861fcc7c0366 |
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| 출처 메모 | uspto-grants-1996_09 |
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