関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Urea | HCID 1176 | — |
| 反応物 | 5-(2-Bromo-acetyl)-thiophene-3-carboxylic acid methyl ester | HCID 53904546 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Methyl 5-(2-amino-1,3-oxazol-5-yl)thiophene-3-carboxylate | HCID 58110273 | 100.9% |
反応手順
5-(2-Bromo-acetyl)-thiophene-3-carboxylic acid methyl ester (0.261 g, 0.99 mmol) was dissolved in DMF (4 mL) and urea (0.131 g, 2.18 mmol) was added. The vessel was purged with nitrogen then sealed and heated by microwave irradiation at 140° C. for 10 minutes. The resultant mixture was diluted with water and extracted with ethyl acetate (×3). The organic phase was washed with lithium chloride (15% aqueous solution) then dried over sodium sulfate, filtered and evaporated to give crude 5-(2-amino-oxazol-5-yl)-thiophene-3-carboxylic acid methyl ester as an orange-brown solid (0.224 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08614209B2 |
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| 出典データセット | uspto-grants-2013_12 |
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| ORD ID | ord-b9aa7d7fcde14863b9e04327bc67a686 |
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| 出典メモ | uspto-grants-2013_12 |
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