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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 274269생성일: 2026년 10월 25일

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

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium hydrideHCID 24758—
반응물6-Chloro-7-methyl-[1,2,4]triazolo[1,5-b]pyridazineHCID 11805158—
반응물3-(N,N-dimethylaminomethylene)aminosulfonyl-2,2-diethyl-1-propanolHCID 53642636—
용매TetrahydrofuranHCID 8028—
생성물1-Butanesulfonamide, 2-ethyl-2-(((7-methyl(1,2,4)triazolo(1,5-b)pyridazin-6-yl)oxy)methyl)-HCID 307378680.7%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05389633
출처 데이터셋uspto-grants-1995_02
ORD IDord-fcf291590c6245a5bef8512c7a58119f
출처 메모uspto-grants-1995_02