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HRID 274282作成日:2026年10月26日

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

https://huagongshe.com/reaction/274282

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 ChlorideHCID 5234—
反応物Sodium hydrideHCID 24758—
反応物3-Hydroxypropane-1-sulfonamideHCID 10486918—
反応物6-Chloro-(1,2,4)triazolo(1,5-b)pyridazineHCID 11240611—
溶媒DimethylformamideHCID 6228—
生成物1-Prpopanesulfonamide, 3-((1,2,4)triazolo(1,5-b)pyridazin-6-yloxy)-HCID 307380152.5%

反応手順

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.

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-ef5441d25a9b42f7b19df8c1f2556881
出典メモuspto-grants-1995_02