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HRID 57690作成日:2026年10月26日

Diisopropylethylamine → Tert-butyl 3-[(6-amino-5-cyanopyridin-2-yl)amino]piperidine-1-carboxylate

https://huagongshe.com/reaction/57690

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物1-BOC-3-AminopiperidineHCID 545809—
反応物2-Amino-6-chloropyridine-3-carbonitrileHCID 20311686—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物Tert-butyl 3-[(6-amino-5-cyanopyridin-2-yl)amino]piperidine-1-carboxylateHCID 57911735—

反応条件

温度130 °C

反応手順

2.15 g (10.7 mmol) of tert-butyl 3-aminopiperidine-1-carboxylate, 1.50 g (9.77 mmol) of 2-amino-6-chloropyridine-3-carbonitrile (Example 28A) and 1.89 g (14.7 mmol) of diisopropylethylamine were suspended in 6 ml of DMSO and heated in a microwave reactor at 130° C. for 8 h. The reaction mixture was diluted with ethyl acetate (100 ml) and water (40 ml), and the organic phase was separated off and washed with saturated aqueous sodium chloride solution (50 ml), dried over magnesium sulfate and concentrated. The residue was chromatographed on silica gel (mobile phase: cyclohexane/ethyl acetate 4:1 to 1:1). This gave 2.04 g (60% of theory) of the product as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434731B2
出典データセットuspto-grants-2016_09
ORD IDord-7b06f89b71e543289fdf5341dc222f0f
出典メモuspto-grants-2016_09