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HRID 397557作成日:2026年10月25日

Ethyl Acetate → 6-[4-[4-(Diphenylmethoxy)piperidino]butylamino][1,2,4]triazolo[4,3-b]pyridazine

https://huagongshe.com/reaction/397557

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物DiisopropylethylamineHCID 81531—
反応物6-Chloro-[1,2,4]triazolo[4,3-b]pyridazineHCID 313624—
反応物1-Piperidinebutanamine, 4-(diphenylmethoxy)-HCID 11739259—
溶媒1-ButanolHCID 263—
生成物6-[4-[4-(Diphenylmethoxy)piperidino]butylamino][1,2,4]triazolo[4,3-b]pyridazineHCID 1552415139.4%

反応手順

1.15 g of 4-(diphenylmethoxy)-1-piperidinebutanamine and 578 mg of 6-chloro[1,2,4]triazolo[4,3-b]pyridazine were dissolved in 20 ml of 1-butanol; 1.17 ml of N-ethyldiisopropylamine was added, followed by refluxing under heating for 14 hours. After cooling, ethyl acetate was added; the reaction mixture was washed with aqueous sodium bicarbonate and saturated saline and dried over magnesium sulfate. After concentration under reduced pressure, the residue was subjected to silica gel column chromatography and eluted with ethyl acetate-methanol-triethylamine (50:5:1). The desired fraction was collected and concentrated under reduced pressure; the residue was crystallized from ethyl acetate and dried to yield 611 mg of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06610694B1
出典データセットuspto-grants-2003_08
ORD IDord-b5bf99c2ffe947f096ecd639dfe4e842
出典メモuspto-grants-2003_08