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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 723793생성일: 2026년 10월 26일

Tributylphosphine → (5S)-3-(4-(1-Benzyl-1,2,5,6-tetrahydropyridin-4-yl)-3-fluorophenyl)-5-(2-oxo-3H-1,3-oxazol-3-ylmethyl)oxazolidin-2-one

https://huagongshe.com/reaction/723793

반응식

참여 물질

역할이름HCID투입량
반응물TributylphosphineHCID 13831—
반응물1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
반응물4-Oxazolin-2-oneHCID 186114—
반응물(5R)-3-(4-(1-Benzyl-1,2,5,6-tetrahydropyridin-4-yl)-3-fluorophenyl)-5-hydroxymethyl-oxazolidin-2-oneHCID 11668069—
용매TetrahydrofuranHCID 8028—
생성물(5S)-3-(4-(1-Benzyl-1,2,5,6-tetrahydropyridin-4-yl)-3-fluorophenyl)-5-(2-oxo-3H-1,3-oxazol-3-ylmethyl)oxazolidin-2-oneHCID 693658340.9%

반응 단계

(5R)-3-(4-(1-Benzyl-1,2,5,6-tetrahydropyridin-4-yl)-3-fluorophenyl)-5-hydroxymethyl-oxazolidin-2-one (2.92 g, 7.3 mM; WO 97-30995) was stirred in tetrahydrofuran (60 ml), and 3H-oxazol-2-one (0.69 g, 8.12 mM) and tributylphosphine (1.77 g, 8.75 mM) were added. The mixture was stirred at 0° under nitrogen, and 1,1′-azodicarbonyldipiperidine (2.06 g, 8.18 mM) was added portionwise. The reaction mixture was allowed to warm to ambient temperature and stirred overnight. The precipitate was filtered off and solvent removed. The resulting oil was dissolved in dichloromethane (30 ml), stirred at 0° for 30 minutes, and further precipitate removed. The filtrate was purified by MPLC on silica eluting with a gradient from 60 to 80% ethyl acetate in isohexane, to give a mixture of starting material and product, which was rechromatographed eluting with 3% MeOH in dichloromethane to give the title compound as a white solid (30 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07141583B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-40c12726f9bf4cc4baf4dae825da0c20
출처 메모uspto-grants-2006_11