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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 576808생성일: 2026년 10월 25일

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

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참여 물질

역할이름HCID투입량
반응물N,N-DimethylethylenediamineHCID 66053—
반응물Methanesulfinic acid sodiumHCID 16212824—
반응물5-(3,6-dimethyl-2,4-dioxo-1-(3-trifluoromethylphenyl)-1,2,3,4-tetrahydropyrimidin-5-yl-4-(methylthio)-1H-pyrazol-1-yl)benzonitrileHCID 86723910—
촉매Benzene;bis(copper(1+));bis(trifluoromethanesulfonate)HCID 2734754—
용매Dimethyl SulfoxideHCID 679—
용매Ethyl AcetateHCID 8857—
생성물5-(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%

반응 조건

온도110 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09040516B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-35e5bd401da64b9c8d637d157f70b4fa
출처 메모uspto-grants-2015_05