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HRID 274266作成日:2026年10月26日

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

https://huagongshe.com/reaction/274266

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3-Hydroxy-2,2-diethyl-1-propanesulfonamideHCID 10559765—
反応物6-Chloro-(1,2,4)triazolo(1,5-b)pyridazineHCID 11240611—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物1-Butanesulfonamide, 2-ethyl-2-(((1,2,4)triazolo(1,5-b)pyridazin-6-yloxy)methyl)-HCID 307378362.7%

反応手順

In 20 ml of dimethylformamide was suspended 0.64 g of 60% sodium hydride in oil, followed by addition of 1.56 g of 3-hydroxy-2,2-diethyl-1-propanesulfonamide and the mixture was stirred under reduced pressure at room temperatue for 30 minutes. Then, 1.24 g of 6-chloro[1,2,4]triazolo[1,5-b]pyridazine was added and the mixture was further stirred at room temperature for 1.5 hours. Following addition of 100 ml of iced water, the reaction mixture was adjusted to pH 6 with 1N-hydrochloric acid and the resulting crystals were collected by filtration and washed with 20 ml of water and 20 ml of ethyl ether. The washed crystals were recrystallized from hot ethanol to provide 1.57 g of the title compound. m.p. 194°-197° 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-e0e8c60a03fc460dba29e649e2ab0274
出典メモuspto-grants-1995_02