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HRID 1984326作成日:2026年10月25日

1-Propanol → 4-(2-aminophenyl)-1,5-dimethyl-1H-pyrazole-3-carbonitrile

https://huagongshe.com/reaction/1984326

反応式

関与物質

役割名称HCID仕込み量
反応物1-PropanolHCID 1031—
反応物Sodium CarbonateHCID 10340—
反応物(2-Aminophenyl)boronic acidHCID 2773216—
反応物4-bromo-1,5-dimethyl-1H-pyrazole-3-carbonitrileHCID 66958966—
触媒TriphenylphosphineHCID 11776—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
生成物4-(2-aminophenyl)-1,5-dimethyl-1H-pyrazole-3-carbonitrileHCID 6695859558.3%

反応条件

温度100 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07544697B2
出典データセットuspto-grants-2009_06
ORD IDord-bb3b039f813645dc8e2b5bdea88b4d31
出典メモuspto-grants-2009_06