関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hexafluorophosphate | HCID 9886 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 2-Azido-4-(3-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid | HCID 86642802 | — |
| 反応物 | HCID 178484285 | HCID 178484285 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 2-Azido-4-(3-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid amide | HCID 86642803 | 83.8% |
反応手順
A solution of 2.20 g (7.01 mmole) of 2-azido-4-(3-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid, 38 mL of dimethylformamide, 3.47 g (8.85 mmole) of 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium, 3-oxide, hexafluorophosphate(1-) (1:1) and 3.75 mL (21.53 mmole) of ethyldiisopropylamine was stirred at room temperature for 23 minutes, then 0.5733 g (10.72 mmole) of ammonium chloride was added. The mixture was stirred for 2.25 hours, then concentrated under reduced pressure and partitioned between 300 mL of ethyl acetate and 75 mL of water. The ethyl acetate layer was washed twice with 60 mL of water, twice with 55 mL of saturated aqueous sodium bicarbonate, once with 50 mL of brine, dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure. The residue was purified by silica gel chromatography, eluting with ethyl acetate-hexanes (gradient 10:90-100-:0) to give 1.841 g 2-azido-4-(3-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid amide as a light yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08044213B2 |
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| 出典データセット | uspto-grants-2011_10 |
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| ORD ID | ord-1b75d78143bf4d98a6034b2c037b5ab2 |
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| 出典メモ | uspto-grants-2011_10 |
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