돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 324967생성일: 2026년 10월 24일

Diisopropylethylamine → 2-[4-(5-Bromo-2-methoxybenzyl)-1-piperazinyl]pyrimidine

https://huagongshe.com/ko/reaction/324967

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물4-Bromo-2-(chloromethyl)-1-methoxybenzeneHCID 10354068—
반응물2-Piperazinylpyrimidine dihydrochlorideHCID 11680272—
용매ChloroformHCID 6212—
생성물2-[4-(5-Bromo-2-methoxybenzyl)-1-piperazinyl]pyrimidineHCID 1240303235%

반응 단계

A mixture of 1.1 g of 2-(chloromethyl)-4-bromoanisole, 1 g of 1-(2-pyrimidyl)piperazine dihydrochloride and 2.0 mL N,N-diisopropylethylamine in 10 mL chloroform was heated at reflux temperature for 2 hr, cooled to room temperature, washed with 1 N NaOH and water. The solvent was removed by evaporation under reduced pressure to yield 3.6 g of 2-[(4-(2-pyrimidinyl)-piperazinyl)methyl]-4-bromoanisole as a white solid which was used in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06221871B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-a6541a6b4c3c406ba75045da9a273aa6
출처 메모uspto-grants-2001_04