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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1394694생성일: 2026년 10월 26일

Triphenylphosphine → (S)-4-Benzyl-3-[(2S)-3-(4-{2-[2-(4-chloro-phenyl)-5-methyl-oxazol-4-yl]-ethoxy}-2-methyl-phenyl)-2-ethoxy-propionyl]-oxazolidin-2-one

https://huagongshe.com/reaction/1394694

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물4-ChlorobenzamideHCID 12084—
반응물Methyl 3-oxovalerateHCID 121699—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물2-(5-Methyl-2-phenyl-4-oxazolyl)ethanolHCID 725585—
반응물2-[2-(4-Chloro-phenyl)-5-methyl-oxazol-4-yl]-ethanolHCID 22273906—
반응물(S)-4-Benzyl-3-[(2S)-2-ethoxy-3-(4-hydroxy-2-methyl-phenyl)-propionyl]-oxazolidin-2-oneHCID 68615907—
용매TetrahydrofuranHCID 8028—
생성물(S)-4-Benzyl-3-[(2S)-3-(4-{2-[2-(4-chloro-phenyl)-5-methyl-oxazol-4-yl]-ethoxy}-2-methyl-phenyl)-2-ethoxy-propionyl]-oxazolidin-2-oneHCID 6928242946.2%

반응 단계

To a ice cold solution of (S)-4-benzyl-3-[(2S)-2-ethoxy-3-(4-hydroxy-2-methyl-phenyl)-propionyl]-oxazolidin-2-one (100 mg, 260 μmol), 2-[2-(4-chloro-phenyl)-5-methyl-oxazol-4-yl]-ethanol (93 mg, 390 μmol) (prepared from methyl 3-oxopentanoate and 4-chloro-benzamide in analogy to the sequence described for the synthesis of 2-(5-methyl-2-phenyl-oxazol-4-yl)-ethanol in M. Scalone, PCT WO 01/79202 A1) and triphenylphosphine (103 mg, 390 mmol) in tetrahydrofuran (2.5 ml) was added diethyl azodicarboxylate (61 μl, 390 μmol). The cooling bath was removed and stirring was continued for 12 h. Evaporation of the solvent under reduced pressure gave a yellow oil which was purified by column chromatography (silica gel, cyclohexane/AcOEt) to give 70 mg (120 μmol, 45%) of the title compound as colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07348349B2
출처 데이터셋uspto-grants-2008_03
ORD IDord-311bd5f31668455eb827eba648eda1b0
출처 메모uspto-grants-2008_03