関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Aminothiazole | HCID 2155 | — |
| 反応物 | Benzenamine, 2-phenoxy- | HCID 75899 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Isocyanatocarbonyl chloride | HCID 119708 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1-(2-Phenoxyphenyl)-5-(thiazol-2-yl)biuret | HCID 59733035 | 55.3% |
反応手順
To a solution of 2-phenoxyaniline (0.46 g, 2.50 mmol) in tetrahydrofuran (20 ml) was added diisopropylethylamine (0.89 ml, 5.00 mmol) and the solution was cooled to −30° C., then N-(chlorocarbonyl)isocyanate (0.3 ml, 3.75 mmol) was slowly added. The mixture was then allowed to warm up to the room temperature during 30 min. 2-Aminothiazole (0.375 g, 3.75 mmol) was added to the reaction mixture and stirred at room temperature for 6 hours. The reaction mixture was concentrated under reduced pressure to afford crude product, which was purified by silica gel chromatography (hexanes:ethyl acetate from 80:20 to 30:70) to afford title compound (0.49 g, 55%) as pale yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07897628B2 |
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| 出典データセット | uspto-grants-2011_03 |
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| ORD ID | ord-3dac87a570b6488e8231d9879114e80b |
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| 出典メモ | uspto-grants-2011_03 |
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