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HRID 27000作成日:2026年10月26日

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

https://huagongshe.com/reaction/27000

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物AcrylonitrileHCID 7855—
反応物6-chloro-2H,3H-[1,2,4]triazolo[4,3-b]pyridazin-3-oneHCID 6407182—
反応物Potassium tert-butoxideHCID 23665647—
溶媒DimethylformamideHCID 6228—
生成物6-Chloro-2-(2-cyanoethyl)-2,3-dihydro-s-triazolo[4,3-b]pyridazin-3-onHCID 2034434611.2%

反応手順

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., 0.12 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04151352
出典データセットuspto-grants-1979_04
ORD IDord-21dc73c207a544c48b3b88e1c2f6a716
出典メモuspto-grants-1979_04