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HRID 37269作成日:2026年10月26日

Water → (2S,4S)-4-acetylthio-1-(4-nitrobenzyloxycarbonyl)-2-[5-(4-nitrobenzyloxycarbonylamino)-1,3-dioxan-2-yl]pyrrolidine

https://huagongshe.com/reaction/37269

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物p-Toluenesulfonic acidHCID 6101—
反応物(2S,4S)-4-acetylthio-2-formyl-1-(4-nitrobenzyloxycarbonyl)pyrrolidineHCID 18638815—
反応物2-(4-Nitrobenzyloxycarbonyl)amino-1,3-propanediolHCID 19934522—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物(2S,4S)-4-acetylthio-1-(4-nitrobenzyloxycarbonyl)-2-[5-(4-nitrobenzyloxycarbonylamino)-1,3-dioxan-2-yl]pyrrolidineHCID 1863881085.7%

反応手順

A solution of 2-(4-nitrobenzyloxycarbonyl)amino-1,3-propanediol (1.42 g), (2S,4S)-4-acetylthio-2-formyl-1-(4-nitrobenzyloxycarbonyl) pyrrolidine (1.00 g) and 4-toluene-sulfonic acid (0.30 g) in toluene was refluxed for 2 hours with removing water under azeotropic condition. The reaction mixture was poured into a mixture of water and ethyl acetate. The organic layer was separated, washed with brine, dried over magnesium sulfate and evaporated. The residue was chromatographed on silica gel (80 ml) and eluted with a mixture of acetone and dichloromethane (1:9, V/V) to give (2S, 4S)-4-acetylthio-1- (4-nitrobenzyloxycarbonyl)-2-[5-(4-nitrobenzyloxycarbonylamino) -1,3-dioxan-2-yl]pyrrolidine (1.47 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05420122
出典データセットuspto-grants-1995_05
ORD IDord-ae36b222e23a4aec9fa43903c97c4233
出典メモuspto-grants-1995_05