関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1-Propanol | HCID 1031 | — |
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | (2-Aminophenyl)boronic acid | HCID 2773216 | — |
| 反応物 | 4-bromo-1,5-dimethyl-1H-pyrazole-3-carbonitrile | HCID 66958966 | — |
| 触媒 | Triphenylphosphine | HCID 11776 | — |
| 触媒 | palladium(II) acetate | HCID 167845 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 4-(2-aminophenyl)-1,5-dimethyl-1H-pyrazole-3-carbonitrile | HCID 66958595 | 58.3% |
反応手順
Triphenylphosphine (2.4 mg, 0.09 mmol) and palladium (II) acetate (7 mg, 0.03 mmol) were added to a mixture of 4-bromo-1,5-dimethyl-1H-pyrazole-3-carbonitrile (0.600 g, 3.00 mmol), 2-aminophenylboronic acid (0.719 g, 5.25 mmol), aqueous sodium carbonate (1.8 mL of 2 M), propanol (5.25 mL) and water (1.1 mL). The reaction was heated under a nitrogen atmosphere at 100° C. for three hours and then allowed to cool to ambient temperature. The work-up procedure described in Part G of Examples 1-4 was followed. The resulting orange oil was purified by chromatography on a HORIZON HPFC system (25+M cartridge, eluting with ethyl acetate/hexane ranging in ratios from 50:50 to 75:25) to provide 371 mg of 4-(2-aminophenyl)-1,5-dimethyl-1H-pyrazole-3-carbonitrile as a pale yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07544697B2 |
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| 出典データセット | uspto-grants-2009_06 |
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| ORD ID | ord-bb3b039f813645dc8e2b5bdea88b4d31 |
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| 出典メモ | uspto-grants-2009_06 |
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