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Ethylamine → 6-(2-Nitro-1-propenyl)imidazo[1,2-a]pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethylamine | HCID 6341 | — |
| 反応物 | Nitroethane | HCID 6587 | — |
| 反応物 | Imidazo[1,2-a]pyridine-6-carbaldehyde | HCID 7164582 | — |
| 触媒 | Butylamine | HCID 8007 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 6-(2-Nitro-1-propenyl)imidazo[1,2-a]pyridine | HCID 53915568 | 11.9% |
反応手順
In 40 ml of ethanol, 6.9 g of 6-imidazo[1,2-a]pyridinecarbaldehyde was stirred under reflux for 14 hours, together with 10.6 g of nitroethane and 30 drops of n-butyl amine. Then, a small quantity of ethyl amine was added thereto and the mixture was stirred under reflux for further 18 hours. After insoluble matter was removed by filtration upon heating, 50 ml of ethanol and 150 ml of ether were further added to remove insoluble matter by filtration. The solvent was removed by distillation under reduced pressure and the residue was recrystallized twice from ethanol to obtain 1.14 g of 6-(2-nitro-1-propenyl)imidazo[1,2-a]pyridine.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04791202 |
| 出典データセット | uspto-grants-1988_12 |
| ORD ID | ord-b67346cabdc447b4ae4a5cb1e2f69ef5 |
| 出典メモ | uspto-grants-1988_12 |