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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2294040생성일: 2026년 10월 25일

1-(3-Chlorophenyl)piperazine → 5-[4-(3-Chloro-phenyl)-piperazin-1-ylmethyl]-pyrimidine-2,4-diamine

https://huagongshe.com/reaction/2294040

반응식

참여 물질

역할이름HCID투입량
반응물1-(3-Chlorophenyl)piperazineHCID 1355—
반응물TriethylamineHCID 8471—
반응물5-(Bromomethyl)pyrimidine-2,4-diamine dihydrobromideHCID 21473608—
용매TetrahydrofuranHCID 8028—
생성물5-[4-(3-Chloro-phenyl)-piperazin-1-ylmethyl]-pyrimidine-2,4-diamineHCID 2147367363%

반응 단계

A solution of 13.5 g (0.050 mol) of 1-(3-chloro-phenyl)-piperazine in 500 ml of tetrahydrofuran was treated with 35 ml (0.25 mol) of triethylamine and 18.2 g (0.050 mol) of 5-bromomethyl-pyrimidine-2,4-diamine dihydrobromide and the mixture was stirred at room temperature under argon for 16 hours. The suspension obtained was suction filtered and the filtrate was completely freed from the solvents. The residue was chromatographed over silica gel with acetonitrile/methanol 1:1 as the eluent and digested in diethyl ether. 10 g (63%) of 5-[4-(3-chloro-phenyl)-piperazin-1-ylmethyl]-pyrimidine-2,4-diamine were obtained as beige crystals; m.p. 222°-226°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05688798
출처 데이터셋uspto-grants-1997_11
ORD IDord-82a69ec5510545d78b21805f22dd62c6
출처 메모uspto-grants-1997_11