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HRID 2389272作成日:2026年10月27日

Cesium carbonate → Tert-butyl 4-(6-cyanopyridin-3-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2389272

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
反応物1-N,2-N-dimethylcyclohexane-1,2-diamineHCID 551074—
反応物5-Bromopyridine-2-carbonitrileHCID 817154—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物Tert-butyl 4-(6-cyanopyridin-3-yl)piperazine-1-carboxylateHCID 67030211—

反応条件

温度120 °C

反応手順

A mixture of the 5-bromopyridine-2-carbonitrile (0.957 g, 5.23 mmol), tert-butyl piperazine-1-carboxylate (1.36 g, 7.32 mmol), cesium carbonate (3.41 g, 10.5 mmol), racemic N,N′-dimethylcyclohexane-1,2-diamine (0.074 g, 0.52 mmol), and copper(I) iodide (0.010 mg, 0.052 mmol) was stirred with 13.1 mL of 1-methylpyrrolidin-2-one and purged with a stream of nitrogen. The reaction was heated to 120° C. for 8 hours. The mixture was diluted with dichloromethane (20 mL) and washed with water (3×20 mL). The organic layer was dried over sodium sulfate, filtered, concentrated, and subjected to purified by silica gel chromatography eluting with 0-50% EtOAc in hexanes. Collection of product containing fractions and removal of solvent yielded to yield tert-butyl 4-(6-cyanopyridin-3-yl)piperazine-1-carboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08273737B2
出典データセットuspto-grants-2012_09
ORD IDord-c9d12e60c76c40658aeafca1f092aea5
出典メモuspto-grants-2012_09