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HRID 846943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/846943

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-toluenesulfonic 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US05138064
出典データセットuspto-grants-1992_08
ORD IDord-ed3ce4ef81c843d895de92213f55301e
出典メモuspto-grants-1992_08