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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 4-(Diphenylmethoxy)-1-piperidinepropaneamine | HCID 10969393 | — |
| 反応物 | N-(6-Chloroimidazo[1,2-b]pyridazine-2-carbonyl) beta-Alanine Ethyl Ester | HCID 22989218 | — |
| 溶媒 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 生成物 | N-[6-[3-[4-(diphenylmethoxy)piperidino]propylamino]imidazo[1,2-b]pyridazine-2-carbonyl]-beta-alanine ethyl ester | HCID 22989251 | 29.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06627630B1 |
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| 出典データセット | uspto-grants-2003_09 |
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| ORD ID | ord-cb34b1c202f64ddeaa54860284c97c76 |
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| 出典メモ | uspto-grants-2003_09 |
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