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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 970310생성일: 2026년 10월 23일

Piperazine → Cgp-74588

https://huagongshe.com/ko/reaction/970310

반응식

참여 물질

역할이름HCID투입량
반응물PiperazineHCID 4837—
반응물4-(Chloromethyl)-N-(4-methyl-3-((4-(3-pyridinyl)-2-pyrimidinyl)amino)phenyl)benzamideHCID 10181075—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물Cgp-74588HCID 9869737—

반응 단계

25.8 g (300 mmol) of piperazine are suspended in a mixture of 25 ml of ethanol and 25 ml of water. After almost a clear solution has formed, 12.9 g (30 mmol) of 4-chloromethyl-N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-2-ylamino)-phenyl]-benzamide are added step by step. The yellow solution is boiled under reflux for 14 hours, cooled to room temperature and filtered over Celite. 100 ml of water is added to the solution, the ethanol is evaporated under vacuum and 30 ml of 1N NaOH is added, leading to crystallization of the product. Drying at 50 mbar and 60° C. yields N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-2-ylamino)-phenyl]-4-piperazin-1-ylmethyl-benzamide; Rf=0.15 (methylene chloride:ethyl acetate:methanol:conc. aqueous ammonium hydroxide solution=60:10:30:2); tR (HPLC)2) 14.6 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07312216B2
출처 데이터셋uspto-grants-2007_12
ORD IDord-bda9621ad94543d4bb433a1bdaebf06b
출처 메모uspto-grants-2007_12