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HRID 703038作成日:2026年10月27日
Tetrahydrofuran → 3-[2-Methyl-3,4-dihydro-3-oxo-4-(propynyl)-2H-1,4-benzoxazin-6-yl]-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedione
https://huagongshe.com/reaction/703038
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Ethyl 3-amino-4,4,4-trifluoro-2-butenoate | HCID 136209 | — |
| 反応物 | 6-isocyanato-2-methyl-3,4-dihydro-3-oxo-4-(2-propynyl)-2H-1,4-benzoxazine | HCID 15029563 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | 3-[2-Methyl-3,4-dihydro-3-oxo-4-(propynyl)-2H-1,4-benzoxazin-6-yl]-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedione | HCID 22151123 | — |
反応手順
A slurry of 1.4 g. of sodium hydride in 25 ml. of dry tetrahydrofuran (THF) was cooled to -10° C. To the cooled and stirred slurry was added a solution of 10.0 g. of ethyl 3-amino-4,4,4-trifluoro-2-butenoate in 50 ml. of THF. The addition of this solution was made over a period of 30 minutes. The resultant light brown reaction mixture was cooled to -70° C. A solution of 13.3 g. of 6-isocyanato-2- methyl-3,4-dihydro-3-oxo-4-(2-propynyl)-2H-1,4-benzoxazine in 75 ml. of THF was added to the chilled reaction mixture over a period of 10 minutes. After stirring at -70° C. for 30 minutes, the temperature was allowed to rise slowly to 10° C. At that point 3.6 ml. of acetic acid was added to the mixture. A beige solid precipitated. 19.0 Grams of the solid was recovered by filtering it from the reaction mixture.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04981508 |
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| 出典データセット | uspto-grants-1991_01 |
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| ORD ID | ord-d05d21b41e2b446ba3921ae65d778a14 |
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| 出典メモ | uspto-grants-1991_01 |
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