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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 397556생성일: 2026년 10월 24일

Diisopropylethylamine → 6-[3-(4-(Diphenylmethoxy)piperidino]propylamino][1,2,4]triazolo[4,3-b]pyridazine

https://huagongshe.com/ko/reaction/397556

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물6-Chloro-[1,2,4]triazolo[4,3-b]pyridazineHCID 313624—
반응물Sodium BicarbonateHCID 516892—
반응물4-(Diphenylmethoxy)-1-piperidinepropaneamineHCID 10969393—
용매1-ButanolHCID 263—
생성물6-[3-(4-(Diphenylmethoxy)piperidino]propylamino][1,2,4]triazolo[4,3-b]pyridazineHCID 1552415048.8%

반응 단계

0.464 g of 6-chloro[1,2,4]triazolo[4,3-b]pyridazine and 1.26 g of 4-(diphenylmethoxy)-1-piperidinepropanamine were suspended in 20 ml of 1-butanol; 0.62 ml of N-ethyldiisopropylamine was added, followed by refluxing under heating for 12 hours. After ice water and sodium hydrogen carbonate were added, the reaction mixture was extracted with ethyl acetate; the extract was washed with saturated saline and dried over magnesium sulfate. After concentration under reduced pressure, the residue was subjected to silica gel column chromatography and eluted with ethyl acetate-methanol-triethylamine (90:10:1). The desired fraction was collected and concentrated; the crystal obtained was washed with ethyl acetate and dried to yield 0.648 g of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06610694B1
출처 데이터셋uspto-grants-2003_08
ORD IDord-4d3147e3bb5844ada7c54f1b19c9dd47
출처 메모uspto-grants-2003_08