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HRID 1394694作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物4-ChlorobenzamideHCID 12084—
反応物Methyl 3-oxovalerateHCID 121699—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物2-(5-Methyl-2-phenyl-4-oxazolyl)ethanolHCID 725585—
反応物2-[2-(4-Chloro-phenyl)-5-methyl-oxazol-4-yl]-ethanolHCID 22273906—
反応物(S)-4-Benzyl-3-[(2S)-2-ethoxy-3-(4-hydroxy-2-methyl-phenyl)-propionyl]-oxazolidin-2-oneHCID 68615907—
溶媒TetrahydrofuranHCID 8028—
生成物(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%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07348349B2
出典データセットuspto-grants-2008_03
ORD IDord-311bd5f31668455eb827eba648eda1b0
出典メモuspto-grants-2008_03