HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 576808Erstellt: 24. Oktober 2026
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/de/reaction/576808
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | N,N-Dimethylethylenediamine | HCID 66053 | — |
| Edukt | 20277-69-4 | HCID 16212824 | — |
| Edukt | 5-(3,6-dimethyl-2,4-dioxo-1-(3-trifluoromethylphenyl)-1,2,3,4-tetrahydropyrimidin-5-yl-4-(methylthio)-1H-pyrazol-1-yl)benzonitrile | HCID 86723910 | — |
| Katalysator | Benzene;bis(copper(1+));bis(trifluoromethanesulfonate) | HCID 2734754 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 5-(3,6-dimethyl-2,4-dioxo-1-(3-trifluoromethylphenyl)-1,2,3,4-tetrahydropyrimidin-5-yl-4-(methylsulfonyl)-1H-pyrazol-1-yl)benzonitrile | HCID 86723912 | 41,4% |
Reaktionsschritte
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).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09040516B2 |
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| Quelldatensatz | uspto-grants-2015_05 |
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| ORD ID | ord-35e5bd401da64b9c8d637d157f70b4fa |
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| Quellennotiz | uspto-grants-2015_05 |
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