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HRID 447791作成日:2026年10月25日

Dichloromethane → 1-(Oxan-4-yl)piperidin-4-amine dihydrochloride

https://huagongshe.com/reaction/447791

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物Potassium CarbonateHCID 11430—
反応物Tetrahydro-4H-pyran-4-oneHCID 121599—
反応物4-(N-Boc-amino)piperidineHCID 723833—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒WaterHCID 962—
溶媒Sodium chloride; waterHCID 57417360—
生成物1-(Oxan-4-yl)piperidin-4-amine dihydrochlorideHCID 45156751—

反応条件

温度0 °C

反応手順

To a solution of 1,1-dimethylethyl 4-piperidinylcarbamate (50 g) was added tetrahydro-4H-pyran-4-one (35.75 g) in dry DCM (1000 ml), then was added sodium triacetoxyborohydride (141 g) portion wise over 10 minutes at about 25° C. The mixture was stirred under nitrogen for about 30 hours, then cooled to 0° C. Water (107 ml) was added portion wise in 20 minutes, followed by saturated aqueous potassium carbonate (178 ml) and saturated brine (178 g in 178 ml). The mixture was stirred for 10 minutes at about 25° C., then the layers were separated and the organic layer washed with saturated brine (3×214 ml). After drying over anhydrous sodium sulphate, the organic layer was concentrated and the residue was treated with 100 ml isopropanol and reconcentrated. The residue was slowly heated to reflux with 11% HCl in isopropanol (200 ml) for 2 hours then cooled to about 25° C. The solid was filtered, and slurry washed with diethyl ether (100 ml), then dried under high vacuum to give the title product (43 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08481566B2
出典データセットuspto-grants-2013_07
ORD IDord-5535cb3c210d43fa9ee7ebd3c3e33089
出典メモuspto-grants-2013_07