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HRID 1169094作成日:2026年10月26日

Diisopropylethylamine → N-[6-[3-[4-(diphenylmethoxy)piperidino]propylamino]imidazo[1,2-b]pyridazine-2-carbonyl]-beta-alanine ethyl ester

https://huagongshe.com/reaction/1169094

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物4-(Diphenylmethoxy)-1-piperidinepropaneamineHCID 10969393—
反応物N-(6-Chloroimidazo[1,2-b]pyridazine-2-carbonyl) beta-Alanine Ethyl EsterHCID 22989218—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物N-[6-[3-[4-(diphenylmethoxy)piperidino]propylamino]imidazo[1,2-b]pyridazine-2-carbonyl]-beta-alanine ethyl esterHCID 2298925129.7%

反応条件

温度95 °C

反応手順

0.649 g of 4-(diphenylmethoxy)-1-piperidinepropanamine and 0.594 g of N-(6-chloroimidazo[1,2-b]pyridazine-2-carbonyl)-β-alanine ethyl ester were dissolved in 7 ml of 1-methyl-2-pyrrolidone; 0.345 ml of N-ethyldiisopropylamine was added, followed by stirring in an oil bath (90-100° C.) for 24 hours. After cooling, ice water was added, followed by extraction with ethyl acetate; the extract was washed with saline, dried over magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography and eluted with ethyl acetate:methanol:triethylamine (370:30:4). The desired fraction was collected and recrystallized from ethyl ether to yield 0.347 g of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06627630B1
出典データセットuspto-grants-2003_09
ORD IDord-cb34b1c202f64ddeaa54860284c97c76
出典メモuspto-grants-2003_09