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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1067518생성일: 2026년 10월 23일

Sodium hydride → 6-[2-[2-[4-(Diphenylmethyl)piperazino] ethoxy]ethoxy]-7-isopropyl[1,2,4]triazolo[1,5-b]pyridazine

https://huagongshe.com/ko/reaction/1067518

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물DecloxizineHCID 71135—
반응물6-Chloro-7-isopropyl[1,2,4]triazolo[1,5-b]pyridazineHCID 22989227—
용매TetrahydrofuranHCID 8028—
생성물6-[2-[2-[4-(Diphenylmethyl)piperazino] ethoxy]ethoxy]-7-isopropyl[1,2,4]triazolo[1,5-b]pyridazineHCID 2298928350.9%

반응 단계

160 mg of 60% sodium hydride in oil was suspended in 20 ml of tetrahydrofuran; 1.20 g of 4-(diphenylmethyl)-1-[2-(2-hydroxyethoxy)ethyl]piperazine was added, followed by heating and refluxing for 1 hour. After cooling, 610 mg of 6-chloro-7-isopropyl[1,2,4]triazolo[1,5-b]pyridazine was added, followed by heating and refluxing for 1 hour. After cooling, ice water was added, followed by extraction with ethyl acetate; the extract was washed with saturated saline and dried with magnesium sulfate. After the dry product was concentrated under reduced pressure, the residue was subjected to silica gel column chromatography and eluted with ethyl acetate:methanol (10:1). The desired fraction was collected; the crystal precipitated was collected by filtration, washed with ethyl ether and dried to yield 790 mg of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06248740B1
출처 데이터셋uspto-grants-2001_06
ORD IDord-ef8602045b2f469eaa20233b91283dd4
출처 메모uspto-grants-2001_06