関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | 5-Formyl-2-thiophenecarboxylic Acid | HCID 818882 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 反応物 | [(2-Acetylaminothiazol-4-yl)methyl](triphenyl)phosphonium chloride | HCID 86092822 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 5-{2-[2-(Acetylamino)-1,3-thiazol-4-yl]vinyl}thiophene-2-carboxylic acid | HCID 86650005 | 58.6% |
反応手順
To a solution of {[2-(acetylamino)-1,3-thiazol-4-yl]methyl}(triphenyl)phosphonium chloride (3.771 g, 8.325 mmol) in anhydrous N,N-dimethylformamide (35 ml) was added potassium tert-butoxide (2.515 g, 22.41 mmol) at 0° C., and the mixture was stirred for 15 min. 5-Formylthiophene-2-carboxylic acid (1.000 g, 6.404 mmol) was added by small portions, and the mixture was stirred at 0° C. for 30 min. The mixture was warmed to room temperature, stirred for 2 hr, and poured into iced water (300 ml). After stirring for 30 min, the mixture was washed twice with ethyl acetate. The aqueous layer was cooled to 0° C., and adjusted to pH 3 by dropwise addition of 6M hydrochloric acid. After stirring at 0-5° C. for 2 hr, the precipitated crystals were collected by filtration, washed 3 times with water, and twice with diisopropyl ether and dried under reduced pressure to give 5-{2-[2-(acetylamino)-1,3-thiazol-4-yl]vinyl}thiophene-2-carboxylic acid (1.104 g, 3.751 mmol, yield 58.6%) as a yellow ocher solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08507690B2 |
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| 出典データセット | uspto-grants-2013_08 |
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| ORD ID | ord-e8dd722b52a647b88e8e9a2d0ea64d7b |
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| 出典メモ | uspto-grants-2013_08 |
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