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HRID 1882953생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1882953

반응식

참여 물질

역할이름HCID투입량
반응물2-Bromo-4-chloroanilineHCID 70110—
반응물DiisopropylethylamineHCID 81531—
반응물TriphosgeneHCID 94429—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
용매DichloromethaneHCID 6344—
생성물2-[(4-Boc-piperazin-1-ylcarbonyl)amino]-5-chlorobromobenzeneHCID 21906538191.1%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06759414B2
출처 데이터셋uspto-grants-2004_07
ORD IDord-58aae5ad023745b5bf7364587b46d5d8
출처 메모uspto-grants-2004_07