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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 397553생성일: 2026년 10월 23일

Glycidol → 6-(2-Oxiranylmethoxy)[1,2,4]triazolo[4,3-b]pyridazine

https://huagongshe.com/ko/reaction/397553

반응식

참여 물질

역할이름HCID투입량
반응물GlycidolHCID 11164—
반응물Sodium hydrideHCID 24758—
반응물6-Chloro-[1,2,4]triazolo[4,3-b]pyridazineHCID 313624—
용매DimethylformamideHCID 6228—
생성물6-(2-Oxiranylmethoxy)[1,2,4]triazolo[4,3-b]pyridazineHCID 2300031632.8%

반응 단계

12.0 g of 2-oxiranylmethanol and 2.50 g of 6-chloro[1,2,4]triazolo[4,3-b]pyridazine were dissolved in 40 ml of N,N-dimethylformamide; under ice cooling, 713 mg of 60% oily sodium hydride was added, followed by stirring at room temperature for 30 minutes. After cold saline was added, the reaction mixture was extracted with ethyl acetate-tetrahydrofuran (1:1) 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 (10:1). The desired fraction was collected and concentrated under reduced pressure; the precipitated crystal was washed with diethyl ether and dried to yield 1.02 g of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06610694B1
출처 데이터셋uspto-grants-2003_08
ORD IDord-8957a2a462814b4bae3c9e5dff4a92b5
출처 메모uspto-grants-2003_08