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HRID 651734作成日:2026年10月26日

Water → 4-(3-Trifluoromethylphenoxy)-2-(3,5-dimethylpyrazol-1-yl)-pyrimidine

https://huagongshe.com/reaction/651734

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物3-(Trifluoromethyl)phenolHCID 7376—
反応物Potassium CarbonateHCID 11430—
反応物3,3-Dichloro-2-propenalHCID 17554—
反応物3,5-Dimethyl-1H-pyrazole-1-carboxamidine mononitrateHCID 198186—
反応物1,1,1,3-Tetrachloro-3-ethoxypropaneHCID 12350822—
触媒3,5-Dimethyl-1H-pyrazole-1-carboxamidine mononitrateHCID 198186—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物4-(3-Trifluoromethylphenoxy)-2-(3,5-dimethylpyrazol-1-yl)-pyrimidineHCID 984062565.8%

反応条件

温度90 °C

反応手順

Water (20 mmoles) is added to a solution of 1,1,1,3-tetrachloro-3-ethoxypropane (10 mmoles) in dimethoxyethane (25 ml). The mixture is stirred for 2 h at 90° C. The resulting mixture is slowly added to a mixture consisting of a 3,5-dimethylpyrazole-1-carboxamidine nitrate (10 mmoles), 3-trifluoromethylphenol (10 mmoles), potassium carbonate (60 mmoles) and dimethoxyethane (50 ml), which is stirred under reflux. When the addition of 3,3-dichloroacrolein solution is completed additional 3,5-dimethylpyrazole-1-carboxamidine nitrate (0.5 mmoles) is added. The reaction mixture is stirred for 10 hours under reflux and subsequently cooled down to ambient temperature, filtered through silica, and the organic phase is concentrated in vacuo. The residue is purified by chromatography on SiO2 (ethyl acetate) to give 2,2 g of a yellow solid. The solid was washed with petrol ether (50 ml) to yield 1,75 g (52%) of colorless crystals having a melting point of 101-102° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06281358B1
出典データセットuspto-grants-2001_08
ORD IDord-6034720edf144f68a5a1fdc9f808c53f
出典メモuspto-grants-2001_08