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HRID 36802作成日:2026年10月24日
Ethyl 3-amino-4,4,4-trifluorocrotonate → 3-(4-chloro-5-ethylsulfonylamino-2-fluorophenyl)-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedione
https://huagongshe.com/ja/reaction/36802
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Ethyl 3-amino-4,4,4-trifluorocrotonate | HCID 5702529 | — |
| 反応物 | Ethyl 4-chloro-5-ethylsulfonylamino-2-fluorocarbanilate | HCID 10903456 | — |
| 反応物 | Sodium Methoxide | HCID 10942334 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 3-(4-chloro-5-ethylsulfonylamino-2-fluorophenyl)-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedione | HCID 11112479 | 77% |
反応手順
1.06 g (5.77 mmol) of ethyl 3-amino-4,4,4-trifluorocrotonate was dissolved in 6.2 ml of N,N-dimethylformamide and 0.82 g (14.4 mmol) of sodium methoxide was added thereto. The reaction mixture was cooled to not higher than 5° C. after 10 minutes, and 1.56 g (4.81 mmol) of ethyl 4-chloro-5-ethylsulfonylamino-2-fluorocarbanilate was added thereto. The resultant mixture was heated to 110° C. and reacted for 4 hours. After the reaction was completed, N,N-dimethylformamide was distilled off and the resultant product was dissolved in water. The thus-obtained solution was washed with diethyl ether 3 times and thereafter concentrated hydrochloric acid was added thereto to pH 2. The precipitated crystals were filtered out, washed with water and dried to obtain 1.54 g of the objective product (yield: 77%) in the form of light yellow crystals.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05416236 |
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| 出典データセット | uspto-grants-1995_05 |
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| ORD ID | ord-dbd92c8c458a4f7abe5413cf41b0ee55 |
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| 出典メモ | uspto-grants-1995_05 |
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