関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl orthoformate | HCID 31214 | — |
| 反応物 | Thiophen-3-amine | HCID 640543 | — |
| 反応物 | 2-cyano-N-(2,4-dichloro-5-methoxyphenyl)acetamide | HCID 16099178 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | 2-cyano-N-(2,4-dichloro-5-methoxyphenyl)-3-(thien-3-ylamino)prop-2-enamide | HCID 69313675 | 26% |
反応手順
To a suspension of 2-cyano-N-(2,4-dichloro-5-methoxyphenyl)acetamide (1.57 g, 6.06 mmol) in 200 mL of iso-propanol was added 3-aminothiophene (600 mg, 6.06 mmol). This mixture was heated to reflux and triethylorthoformate (6.5 mL, 39.1 mmol) was added dropwise. The reaction mixture was heated at reflux overnight. Additional 3-aminothiophene (214 mg, 2.16 mmol) was added and the reaction mixture was heated at reflux for 5 hours. Additional 3-aminothiophene (100 mg, 1.01 mmol) was added and the reaction mixture was heated at reflux for 2.5 hours. The mixture was allowed to cool to room temperature and the solid was collected by filtration, washed with iso-propanol to give 572 mg (26%) of 2-cyano-N-(2,4-dichloro-5-methoxyphenyl)-3-(thien-3-ylamino)prop-2-enamide as a tan solid, mp >250° C.; MS 366.0, 368.2 (M−H)−
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07297795B2 |
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| 出典データセット | uspto-grants-2007_11 |
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| ORD ID | ord-5a886353dd1545818b1b995b5618d85a |
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| 出典メモ | uspto-grants-2007_11 |
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