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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

반응식

참여 물질

역할이름HCID투입량
반응물TributylphosphineHCID 13831—
반응물1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
반응물(R)-5-(hydroxymethyl)-3-(4-morpholinophenyl)oxazolidin-2-oneHCID 20725693—
반응물tert-Butyl 1,2-oxazol-3-ylcarbamateHCID 21992950—
용매TetrahydrofuranHCID 8028—
생성물5(S)-(Isoxazol-3-yl-aminomethyl)-3-(4-morpholinophenyl)-oxazolidin-2-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06734200B1
출처 데이터셋uspto-grants-2004_05
ORD IDord-4c95cb43c66d4c578150478395b167e3
출처 메모uspto-grants-2004_05