関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Oxamic Acid | HCID 974 | — |
| 反応物 | 4-Methylmorpholine | HCID 7972 | — |
| 反応物 | Ethyl chloroformate | HCID 10928 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | 3-Cyclopentyloxy-4-methoxyphenethylamine | HCID 11276394 | — |
| 溶媒 | 1,2-Dimethoxyethane | HCID 8071 | — |
| 生成物 | N-[2-(3-Cyclopentyloxy-4-methoxyphenyl)ethyl]oxamide | HCID 9861348 | 30% |
反応手順
To a suspension of oxamic acid (1.76 g, 20 mmol) in 1,2-dimethoxyethane (75 mL) under an argon atmosphere was added dropwise N-methylmorpholine (2.55 mL, 23 mmol) followed by ethyl chloroformate (2.20 mL, 23 mmol). After stirring for 1 h at room temperature, a solution of 2-(3-cyclopentyloxy-4-methoxy-phenyl)ethylamine (4.65 g, 20 mmol) in 1,2-dimethoxyethane (30 mL) was added over 5 min, and the resulting mixture was stirred for 2 h. Saturated aqueous ammonium chloride was added and the solvent was removed under reduced pressure. The solid residue was dissolved in methanol/methylene chloride, washed successively with water, 10% hydrochloric acid, aqueous sodium bicarbonate and water and dried (potassium carbonate). The solvent was removed in vacuo and the residue was purified by flash chromatography, eluting with 1% i-propanol/methylene chloride to provide the oxamide (1.82 g, 30%): m.p. 175°-175.5° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05393788 |
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| 出典データセット | uspto-grants-1995_02 |
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| ORD ID | ord-11799f87b34444998fe8615eefb7b91c |
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| 出典メモ | uspto-grants-1995_02 |
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