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HRID 274269作成日:2026年10月26日

Hydrochloric Acid → 1-Butanesulfonamide, 2-ethyl-2-(((7-methyl(1,2,4)triazolo(1,5-b)pyridazin-6-yl)oxy)methyl)-

https://huagongshe.com/reaction/274269

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Sodium hydrideHCID 24758—
反応物6-Chloro-7-methyl-[1,2,4]triazolo[1,5-b]pyridazineHCID 11805158—
反応物3-(N,N-dimethylaminomethylene)aminosulfonyl-2,2-diethyl-1-propanolHCID 53642636—
溶媒TetrahydrofuranHCID 8028—
生成物1-Butanesulfonamide, 2-ethyl-2-(((7-methyl(1,2,4)triazolo(1,5-b)pyridazin-6-yl)oxy)methyl)-HCID 307378680.7%

反応手順

To a solution of 1.38 g of 3-(N,N-dimethylamino-methylene)aminosulfonyl-2,2-diethyl-1-propanol in 30 ml of tetrahydrofuran was added 0.23 g of 60% sodium hydride in oil and the mixture was stirred at room temperature for 1 hour. To this reaction mixture was added 0.74 g of 6-chloro-7-methyl[1,2,4]triazolo[1,5-b]pyridazine and the mixture was refluxed with stirring for 1 hour. After cooling, the reaction mixture was adjusted to pH 6 with 1N-hydrochloric acid and extracted with ethyl acetate-tetrahydrofuran (1:1). The extract was washed with water and dried and the solvent was distilled off. To the residue was added 14 ml of 6N-hydrochloric acid and the mixture was stirred at 110° C. for 30 minutes. After cooling, 100 ml of water was added to the reaction mixture and the resulting crystals were recovered by filtration and recrystallized from methanol to provide 1.16 g of the title compound. m.p. 208°-209° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05389633
出典データセットuspto-grants-1995_02
ORD IDord-fcf291590c6245a5bef8512c7a58119f
出典メモuspto-grants-1995_02