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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 274282생성일: 2026년 10월 24일

Hydrochloric Acid → 1-Prpopanesulfonamide, 3-((1,2,4)triazolo(1,5-b)pyridazin-6-yloxy)-

https://huagongshe.com/ko/reaction/274282

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium ChlorideHCID 5234—
반응물Sodium hydrideHCID 24758—
반응물3-Hydroxypropane-1-sulfonamideHCID 10486918—
반응물6-Chloro-(1,2,4)triazolo(1,5-b)pyridazineHCID 11240611—
용매DimethylformamideHCID 6228—
생성물1-Prpopanesulfonamide, 3-((1,2,4)triazolo(1,5-b)pyridazin-6-yloxy)-HCID 307380152.5%

반응 단계

In 12 ml of dimethylformamide was suspended 0.48 g of 60% sodium hydride in oil followed by addition of 0.835 g of 3-hydroxy-1-propanesulfonamide and the mixture was stirred under reduced pressure at room temperature for 30 minutes. Then, 0.928 g of 6-chloro[1,2,4]triazolo[1,5-b]pyridazine was added and the mixture was further stirred at room temperature for 18 hours. Following addition of 40 ml of ice water, the reaction mixture was adjusted to pH6 with 1N-hydrochloric acid then saturated with sodium chloride. The aqueous layer was extracted with tetrahydrofuran and the extract was dried over magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was crystallized from ethyl ether. The washed crystals were recrystallized from hot methanol to provide 0.811 g of title compound. m.p. 145°-147° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05389633
출처 데이터셋uspto-grants-1995_02
ORD IDord-ef5441d25a9b42f7b19df8c1f2556881
출처 메모uspto-grants-1995_02