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HRID 988622作成日:2026年10月27日

2-Bromo-4-chloroaniline → 2-[(4-Boc-piperazin-1-ylcarbonyl)amino]-5-chlorobromobenzene

https://huagongshe.com/reaction/988622

反応式

関与物質

役割名称HCID仕込み量
反応物2-Bromo-4-chloroanilineHCID 70110—
反応物DiisopropylethylamineHCID 81531—
反応物TriphosgeneHCID 94429—
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
溶媒DichloromethaneHCID 6344—
生成物2-[(4-Boc-piperazin-1-ylcarbonyl)amino]-5-chlorobromobenzeneHCID 21906538191.1%

反応手順

To a stirring solution of triphosgene (2.7 g, 9.0 mmol) in dichloromethane (100 mL) was added, dropwise via an addition funnel, a solution of 2-bromo-4-chloroaniline (5 g, 24.2 mmol) and N,N-diisopropylethylamine (6.9 g, 53.2 mmol) in dichloromethane (50 mL). After complete addition and an additional hour, a solution of N-Boc-piperazine (5 g, 26.6 mmol) in dichloromethane (50 mL) was added. After stirring overnight, the solvent was removed in vacuo and the residue was partitioned between ethyl acetate and water. The organic phase was separated and washed consecutively with 1 M citric acid, brine, sat. aq sodium bicarbonate and finally with brine, then dried with MgSO4, filtered and concentrated in vacuo. The residue was then dissolved in a minimal amount of chloroform and chromatographed over silica gel, eluting with 20% ethyl acetate in hexanes followed by 30% ethyl acetate in hexanes. The product containing fractions were combined and concentrated in vacuo and the resulting solid was suspended in diethyl ether, sonicated and then filtered and dried in vacuo to give 7.2 g (71%) of a white powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06635657B1
出典データセットuspto-grants-2003_10
ORD IDord-d7e4e3d9262843f78eda677a727a6669
出典メモuspto-grants-2003_10