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HRID 1092016作成日:2026年10月25日

5-Bromothiophene-2-carbaldehyde → Tert-butyl 4-(5-formylthiophen-2-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1092016

反応式

関与物質

役割名称HCID仕込み量
反応物5-Bromothiophene-2-carbaldehydeHCID 78428—
反応物DiisopropylethylamineHCID 81531—
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
溶媒Dimethyl SulfoxideHCID 679—
生成物Tert-butyl 4-(5-formylthiophen-2-yl)piperazine-1-carboxylateHCID 2806529873%

反応条件

温度130 °C

反応手順

A mixture of 5-bromothiophene-2-carboxaldehyde (3.82 g, 20.0 mmol), tert-butyl piperazine-1-carboxylate (4.1 g, 22.0 mmol), N-ethyl-N,N-diisopropylamine (7.0 ml, 40.0 mmol) and dimethylsulphoxide (5.0 ml) were stirred at 130° C. under an atmosphere of nitrogen for 18 h. The cooled mixture was partitioned between ethyl acetate and water. The organics were washed with water, brine, dried over magnesium sulphate and evaporated. The resultant dark red solid was purified by silica column chromatography, eluting with dichloromethane followed by ethyl acetate/dichloromethane (15%) to give tert-butyl 4-(5-formylthien-2-yl)piperazine-1-carboxylate (4.3 g, 73%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08129391B2
出典データセットuspto-grants-2012_03
ORD IDord-a9fc2d5b627f45e1b056a3d71487c00f
出典メモuspto-grants-2012_03