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HRID 732276作成日:2026年10月25日

Tert-butyl 3-(benzyloxycarbonylamino)-4-hydroxy-pyrrolidine-1-carboxylate → 1-Methyl-4-(methylamino)pyrrolidin-3-OL

https://huagongshe.com/reaction/732276

反応式

関与物質

役割名称HCID仕込み量
反応物Tert-butyl 3-(benzyloxycarbonylamino)-4-hydroxy-pyrrolidine-1-carboxylateHCID 20691380—
反応物Aluminium lithium hydrideHCID 21226445—
溶媒TetrahydrofuranHCID 8028—
生成物1-Methyl-4-(methylamino)pyrrolidin-3-OLHCID 6846507618%

反応条件

温度0 °C

反応手順

LAH (1.40 g, 35.0 mmol) is slowly added to a stirred solution of 3-benzyloxycarbonylamino-4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester in THF (15 ml) at room temperature. The reaction mixture is heated to reflux under N2 for 2 hours and then cooled to 0° C. The reaction mixture is quenched by the slow addition of Na2SO4.10H2O, warmed to room temperature, diluted with ethyl acetate and filtered through Celite. The filtrate is concentrated and purified on a silica gel column (10:1:0.5 methylene chloride, MeOH, 30% NH4OH solution) to yield 0.21 g (18% for two steps) 1-methyl-4-methylamino-pyrrolidin-3-ol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07585975B2
出典データセットuspto-grants-2009_09
ORD IDord-517b1a151371432f8a873afce9e63243
出典メモuspto-grants-2009_09