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HRID 448736作成日:2026年10月25日
Triethylamine → 1-[[(2-Oxo-1-imidazolidinyl)carbonyl]amino]cyclohexanecarboxylic acid phenylmethyl ester
https://huagongshe.com/reaction/448736
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2-Oxoimidazolidine-1-carbonyl chloride | HCID 83241 | — |
| 反応物 | Benzyl 1-aminocyclohexanecarboxylate | HCID 15176238 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 1-[[(2-Oxo-1-imidazolidinyl)carbonyl]amino]cyclohexanecarboxylic acid phenylmethyl ester | HCID 57672822 | 82.2% |
反応手順
1.38 g (9.3 mmol) of 2-oxo-1-imidazolidinecarbonyl chloride was added to a solution of 2.17 g (9.3 mmol) of 1-aminocyclohexanecarboxylic acid phenylmethyl ester and 1.04 g (10 mmol) of triethylamine in 100 ml of chloroform, and the mixture was stirred at 60° C. for 4 days. The reaction solution was successively washed with water, a 10% aqueous potassium hydrogensulfate solution, a saturated aqueous sodium hydrogencarbonate solution and saturated brine, and it was dried with anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the obtained crystal was washed with diethyl ether to obtain 2.64 g (82%) 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 | US08481725B2 |
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| 出典データセット | uspto-grants-2013_07 |
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| ORD ID | ord-8c73fb65a01a4bbc84455997d35dca8d |
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| 出典メモ | uspto-grants-2013_07 |
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