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HRID 1744561作成日:2026年10月27日

Triethylamine → N-(3-Cyano-4-isobutoxyphenyl)-1-(4-fluorophenyl)-5-methylpyrazole-4-carboxamide

https://huagongshe.com/reaction/1744561

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Diethyl cyanophosphonateHCID 76257—
反応物1-(4-fluorophenyl)-5-methyl-1H-pyrazole-4-carboxylic acidHCID 4270263—
反応物5-Amino-2-isobutoxybenzonitrileHCID 19366028—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物N-(3-Cyano-4-isobutoxyphenyl)-1-(4-fluorophenyl)-5-methylpyrazole-4-carboxamideHCID 982187334.2%

反応手順

1-(4-Fluorophenyl)-5-methylpyrazole-4-carboxylic acid (2 g), 5-amino-2-isobutoxybenzonitrile (1.7 g), triethylamine (2.7 g) and diethyl cyanophosphate (2.2 g) were added to dimethylformamide (20 ml) and the mixture was stirred at room temperature for 1 h. The reaction mixture was added into water and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, after which the solvent was evaporated under reduced pressure. Diisopropyl ether was added to the residue to allow crystallization. The crystals were recrystallized from a mixed solvent of ethyl acetate-n-hexane to give the title compound (1.2 g), melting point: 177–178° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07015218B1
出典データセットuspto-grants-2006_03
ORD IDord-b2fd98bfe31741838dc65fa990f303a6
出典メモuspto-grants-2006_03