Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1582370생성일: 2026년 10월 27일
Tributylphosphine → 5(S)-(Isoxazol-3-yl-aminomethyl)-3-(4-morpholinophenyl)-oxazolidin-2-one
https://huagongshe.com/reaction/1582370
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tributylphosphine | HCID 13831 | — |
| 반응물 | 1,1'-(Azodicarbonyl)dipiperidine | HCID 73042 | — |
| 반응물 | (R)-5-(hydroxymethyl)-3-(4-morpholinophenyl)oxazolidin-2-one | HCID 20725693 | — |
| 반응물 | tert-Butyl 1,2-oxazol-3-ylcarbamate | HCID 21992950 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5(S)-(Isoxazol-3-yl-aminomethyl)-3-(4-morpholinophenyl)-oxazolidin-2-one | HCID 69890495 | — |
반응 단계
5(R)-Hydroxymethyl-3-(4-morpholinophenyl)oxazolidin-2-one (prepared by analogy to the 3-fluoro compound—see WO95/07271; 0.50 g, 1.80 mmol), 3-t-butyloxycarbonylamino-isoxazole (0.50 g, 2.70 mmol), tri-n-butylphosphine (0.66 ml, 2.70 mmol), and 1,1′-(azodicarbonyl)-di-piperidine (0.68 g, 2.70 mmol) were reacted in anhydrous THF (30 ml) using the general method of Reference Example 15. The reaction was then purified by MPLC (Merck 9385 silica, 70% ethyl acetate in iso-hexane) and the solvent removed under reduced pressure to give a solid which was triturated with ether to give the title compound as an off-white solid. 1H-NMR (300 MHz, DMSO-d6): δ=1.50 (s, 9H), 3.08 (t, 4H), 3.70-3.80 (m, 5H), 3.93-4.01 (m, 1H), 4.14-4.30 (m, 2H), 4.95 (m, 1H), 6.88 (s, 1H), 6.99 (d, 2H), 7.40 (d, 2H), 8.81 (s, 1H). MS: ESP+ (M+H)+=445.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06734200B1 |
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| 출처 데이터셋 | uspto-grants-2004_05 |
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| ORD ID | ord-4c95cb43c66d4c578150478395b167e3 |
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| 출처 메모 | uspto-grants-2004_05 |
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