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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1986220생성일: 2026년 10월 27일

1-(3-Aminopropyl)-4-methylpiperazine → [4-(Benzo[b]thiophen-2-yl)-pyrimidin-2-yl]-[3-(4-methylpiperazin-1-yl)-propyl]-amine tri-hydrochloride

https://huagongshe.com/reaction/1986220

반응식

참여 물질

역할이름HCID투입량
반응물1-(3-Aminopropyl)-4-methylpiperazineHCID 78328—
반응물4-(1-Benzothiophen-2-yl)-2-chloropyrimidineHCID 14745025—
용매1,4-DioxaneHCID 31275—
생성물[4-(Benzo[b]thiophen-2-yl)-pyrimidin-2-yl]-[3-(4-methylpiperazin-1-yl)-propyl]-amine tri-hydrochlorideHCID 68855962213.5%

반응 단계

1-(3-Aminopropyl)-4-methylpiperazine (3.02 g, 19.2 mmol) is added to a stirred suspension of 4-(benzo[b]thiophen-2-yl)-2-chloro-pyrimidine (2.06 g, 8.34 mmol) in anhydrous 1,4-dioxane (25 mL) at ambient temperature under nitrogen. The resultant mixture is heated in an oil bath at 95° C. for 28 hours. At ambient temperature the mixture is concentrated and subject to chromatographic purification on silica gel, eluting with 2 M NH3/CH3OH in dichloromethane 0-6%, to give the free base of the title compound as a white solid (2.83 g, 92% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07547691B2
출처 데이터셋uspto-grants-2009_06
ORD IDord-c84c9e76168d4ed0b7b9f3c27344efb4
출처 메모uspto-grants-2009_06