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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2049862생성일: 2026년 10월 26일

Water → 6-Chloro-2-(2-cyanoethyl)-2,3-dihydro-s-triazolo[4,3-b]pyridazin-3-on

https://huagongshe.com/reaction/2049862

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물AcrylonitrileHCID 7855—
반응물6-chloro-2H,3H-[1,2,4]triazolo[4,3-b]pyridazin-3-oneHCID 6407182—
반응물Potassium tert-butoxideHCID 23665647—
용매DimethylformamideHCID 6228—
생성물6-Chloro-2-(2-cyanoethyl)-2,3-dihydro-s-triazolo[4,3-b]pyridazin-3-onHCID 2034434611.2%

반응 단계

To a solution of 6-chloro-2,3-dihydro-s-triazolo[4,3-b]pyridazin-3-on [P. Francabilla and F. Lauria, J. Het. Chem. 8, 415 (1971)] (17 g., 0.1 mole) in dry DMF (300 ml.) was added potassium tert.-butoxide (0.5 g., 4.5 m.moles) with stirring. Acrylonitrile (6.6 g., 0.2 mole) in dry DMF (10 ml.) was added to the mixture. The mixture was stirred at 100°-110° C. for 24 hours, then poured into water (700 ml.) and extracted with ethyl acetate (5×400 ml.). The organic extracts were combined, dried over Na2SO4 and evaporated. The residue was crystallized from ethyl acetate to give light yellow needles of 6-chloro-2-(2-cyanoethyl)-2,3-dihydro-s-triazolo[4,3-b]pyridazin-3-on (2.5 g., 11%). M.p. 166°-168° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04198506
출처 데이터셋uspto-grants-1980_04
ORD IDord-118cee0fe68a4965a14c75aafb9cbd68
출처 메모uspto-grants-1980_04