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HRID 576808作成日:2026年10月26日

N,N-Dimethylethylenediamine → 5-(3,6-dimethyl-2,4-dioxo-1-(3-trifluoromethylphenyl)-1,2,3,4-tetrahydropyrimidin-5-yl-4-(methylsulfonyl)-1H-pyrazol-1-yl)benzonitrile

https://huagongshe.com/reaction/576808

反応式

関与物質

役割名称HCID仕込み量
反応物N,N-DimethylethylenediamineHCID 66053—
反応物Methanesulfinic acid sodiumHCID 16212824—
反応物5-(3,6-dimethyl-2,4-dioxo-1-(3-trifluoromethylphenyl)-1,2,3,4-tetrahydropyrimidin-5-yl-4-(methylthio)-1H-pyrazol-1-yl)benzonitrileHCID 86723910—
触媒Benzene;bis(copper(1+));bis(trifluoromethanesulfonate)HCID 2734754—
溶媒Dimethyl SulfoxideHCID 679—
溶媒Ethyl AcetateHCID 8857—
生成物5-(3,6-dimethyl-2,4-dioxo-1-(3-trifluoromethylphenyl)-1,2,3,4-tetrahydropyrimidin-5-yl-4-(methylsulfonyl)-1H-pyrazol-1-yl)benzonitrileHCID 8672391241.4%

反応条件

温度110 °C

反応手順

To a solution of the compound prepared in Example 269 (2.84 g) in dimethyl sulfoxide (9.8 ml) were added methanesulfinic acid sodium (2.00 g), copper trifluoromethanesulfonate benzene complex (1.24 g), N,N-dimethylethylenediamine (529 mg) and the resulting mixture was stirred at 110° C. for seven hours. The reaction mixture was diluted with ethyl acetate (300 ml), and the organic layer was washed with 10% ammonia water (50 ml) and saturated saline (50 ml), dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate) to afford 4-(5-(3,6-dimethyl-2,4-dioxo-1-(3-trifluoromethylphenyl)-1,2,3,4-tetrahydropyrimidin-5-yl-4-(methylsulfonyl)-1H-pyrazol-1-yl)benzonitrile (1.25 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09040516B2
出典データセットuspto-grants-2015_05
ORD IDord-35e5bd401da64b9c8d637d157f70b4fa
出典メモuspto-grants-2015_05