関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Diphenylphosphinamide | HCID 853560 | — |
| 反応物 | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| 反応物 | 3-(difluoromethyl)-N-phenyl-1H-pyrrole-2-carboxamide | HCID 70979488 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 1-Amino-3-(difluoromethyl)-N-phenyl-1H-pyrrole-2-carboxamide | HCID 70979555 | 38% |
反応手順
1.1 ml (1.1 mmol) of a 1M solution of lithium bis(trimethylsilyl)amide was added to a solution of 3-(difluoromethyl)-N-phenyl-1H-pyrrole-2-carboxamide (100 mg, 0.42 mmol) and DPPONH2 (P,P-diphenylphosphinic amide, available from Sigma Aldrich®, cat. no. 5994-87-6) (250 mg, 1,1 mmol) in DMF (4 mL) at room temperature. A thick suspension formed and additional 4 mL of DMF were added. The mixture was stirred at room temperature for 1 hour and then it was poured into 50 mL of water and extracted with ethyl acetate. The aqueous layer was further extracted with ethyl acetate (2×). The combined organic layer was washed with water and brine and was dried over sodium sulphate, filtered and concentrated. The crude product was purified by flash chromatography (0% to 33% AcOEt/Hexanes) to yield 40 mg (38% yield) of the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09340547B2 |
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| 出典データセット | uspto-grants-2016_05 |
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| ORD ID | ord-41ba3a249a234264a3f78ed7a26965f2 |
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| 出典メモ | uspto-grants-2016_05 |
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