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HRID 498922作成日:2026年10月26日

Dimethylformamide → 1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboxylic acid (3-tert-butyl-2-vinylphenyl)amide

https://huagongshe.com/reaction/498922

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物TriethylamineHCID 8471—
反応物1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxylic acidHCID 2775665—
反応物3-Tert-butyl-2-ethenylanilineHCID 68463211—
溶媒DichloromethaneHCID 6344—
生成物1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboxylic acid (3-tert-butyl-2-vinylphenyl)amideHCID 11617265—

反応手順

197 mg (1,01 mmol) 1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboxylic acid and 135 mg (1,07 mmol) oxalylic acid chloride are dissolved in 8 ml methylenechloride. The solution is stirred for 3 hours at room temperature in the presence of a catalytic amount of dimethylformamide (DMF). After this the solution is slowly added to a solution consisting of 180 mg (1,01 mmol) 3-tert-butyl-2-vinyl-phenylamine, 155 mg (1,52 mmol) triethylamine and 7 ml methylenechloride. The resulting reaction mixture is then stirred at room temperature for 16 hours. After removal of the solvent in a water jet vacuum, the residue is purified by flash chromatography over silicagel (eluent: hexane/ethylacetate 2:1). This gives 0,27 g 1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboxylic acid (3-tert-butyl-2-vinylphenyl)amide in the form of a colourless solid (m.p. 118-119° C.; 76% of theory).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07767625B2
出典データセットuspto-grants-2010_08
ORD IDord-2ef4725139d742d496e09cfb23d1adca
出典メモuspto-grants-2010_08