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HRID 274272作成日:2026年10月26日

6-Hydroxy-5,5-diethyl-1-hexanesulfonamide → 1-Heptanesulfonamide, 5-ethyl-5-((7-methyl(1,2,4)triazolo(1,5-b)pyridazin-6-yl)oxy)methyl)-

https://huagongshe.com/reaction/274272

反応式

関与物質

役割名称HCID仕込み量
反応物6-Hydroxy-5,5-diethyl-1-hexanesulfonamideHCID 10657530—
反応物6-Chloro-7-methyl-[1,2,4]triazolo[1,5-b]pyridazineHCID 11805158—
生成物1-Heptanesulfonamide, 5-ethyl-5-((7-methyl(1,2,4)triazolo(1,5-b)pyridazin-6-yl)oxy)methyl)-HCID 3073790—

反応手順

Using 6-hydroxy-5,5-diethyl-1-hexanesulfonamide and 6-chloro-7-methyl[1,2,4]triazolo[1,5-b]pyridazine, the same reaction was conducted as in Example 5 to produce the title compound. m.p. 132°-133° 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-31fc2eefdb594f198f1f9e3aef219c49
出典メモuspto-grants-1995_02