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HRID 397556作成日:2026年10月25日

Diisopropylethylamine → 6-[3-(4-(Diphenylmethoxy)piperidino]propylamino][1,2,4]triazolo[4,3-b]pyridazine

https://huagongshe.com/reaction/397556

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物6-Chloro-[1,2,4]triazolo[4,3-b]pyridazineHCID 313624—
反応物Sodium BicarbonateHCID 516892—
反応物4-(Diphenylmethoxy)-1-piperidinepropaneamineHCID 10969393—
溶媒1-ButanolHCID 263—
生成物6-[3-(4-(Diphenylmethoxy)piperidino]propylamino][1,2,4]triazolo[4,3-b]pyridazineHCID 1552415048.8%

反応手順

0.464 g of 6-chloro[1,2,4]triazolo[4,3-b]pyridazine and 1.26 g of 4-(diphenylmethoxy)-1-piperidinepropanamine were suspended in 20 ml of 1-butanol; 0.62 ml of N-ethyldiisopropylamine was added, followed by refluxing under heating for 12 hours. After ice water and sodium hydrogen carbonate were added, the reaction mixture was extracted with ethyl acetate; the extract was washed with 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 (90:10:1). The desired fraction was collected and concentrated; the crystal obtained was washed with ethyl acetate and dried to yield 0.648 g 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-4d3147e3bb5844ada7c54f1b19c9dd47
出典メモuspto-grants-2003_08