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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1067494생성일: 2026년 10월 24일

4-Benzhydryl-1-piperazinepropanol → 6-[3-[4-(Diphenylmethyl)piperazino]propoxy]-7-isopropyl[1,2,4]triazolo[1,5-b]pyridazine dihydrochloride

https://huagongshe.com/ko/reaction/1067494

반응식

참여 물질

역할이름HCID투입량
반응물4-Benzhydryl-1-piperazinepropanolHCID 15524146—
반응물6-Chloro-7-isopropyl[1,2,4]triazolo[1,5-b]pyridazineHCID 22989227—
반응물Sodium t-butoxideHCID 23676156—
용매TetrahydrofuranHCID 8028—
생성물6-[3-[4-(Diphenylmethyl)piperazino]propoxy]-7-isopropyl[1,2,4]triazolo[1,5-b]pyridazine dihydrochlorideHCID 22989368142.7%

반응 단계

4-(Diphenylmethyl)-1-piperazinepropanol (466 mg) was dissolved in dried tetrahydrofuran (10 ml), followed by addition of sodium t-butoxide (173 mg). The mixture was refluxed under heating for 30 minutes. After the mixture was cooled, 6-chloro-7-isopropyl[1,2,4]triazolo[1,5-b]pyridazine (295 mg) was added thereto. The resulting mixture was refluxed for 3 hours under heating. After cooling, ice-water was added to the mixture, followed by extraction with ethyl acetate. The extract was washed with an aqueous sodium chloride saturated solution, dried over magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography and eluted with a mixture of ethyl acetate and methanol (10:1). Fractions containing the objective compound were collected and dissolved in ethanol (10 ml), followed by addition of 1N-HCl (3 ml). The mixture was concentrated under reduced pressure. The resulting crystals were recrystalized from ethyl acetate to yield the title compound (582 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06248740B1
출처 데이터셋uspto-grants-2001_06
ORD IDord-efb4ee823bb746b4ba6b8e0cef3d9971
출처 메모uspto-grants-2001_06