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HRID 745182作成日:2026年10月26日
1,1'-Carbonyldiimidazole → N-(1-Methylethyl)-N'-[2-[methyl-(2-phenylethyl)amino]ethyl]-N-[2-(phenylsulfonyl)ethyl]urea hemihydrate
https://huagongshe.com/reaction/745182
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| 反応物 | N-Methyl-N-(2-phenylethyl)ethane-1,2-diamine | HCID 12488261 | — |
| 反応物 | N-(2-phenylsulfonylethyl)-2-propanamine | HCID 13655034 | — |
| 反応物 | Ethylacetate acetone | HCID 21584569 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Chloroform ether | HCID 21911965 | — |
| 生成物 | N-(1-Methylethyl)-N'-[2-[methyl-(2-phenylethyl)amino]ethyl]-N-[2-(phenylsulfonyl)ethyl]urea hemihydrate | HCID 70419535 | — |
反応手順
A solution of 1,1'-carbonyldiimidazole (8.12 g, 0.05 mole) and N-methyl-N-(2-phenylethyl)-1,2-ethanediamine, 8.0 g (0.0045 mole) in 300 ml of tetrahydrofuran was stirred for 2 hours at room temperature. To the mixture was added 9.37 g (0.0412 mole) of 1-methyl-N-[2-(phenylsulfonyl)ethyl]ethanamine and the reaction was heated at gentle reflux overnight. The reaction was stripped to dryness and dissolved in chloroform-diethyl ether (50-50 v/v) and extracted with water. The organic phase was extracted with 1N sulfuric acid. (Approximately half the product was extracted with acid and half remained in the organic layer). The organic layer was extracted with dilute sodium hydroxide, dried, filtered, and the solvent removed to give an oil. The oil was subjected to column chromatography on Silica Gel using acetone-ethyl acetate as a eluant. This furnished 0.5 g (2.8%) of oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04597902 |
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| 出典データセット | uspto-grants-1986_07 |
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| ORD ID | ord-0ae0a9dc6c934b61a16309de49d0b18f |
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| 出典メモ | uspto-grants-1986_07 |
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