5-Ethyl-6-(3,5-dimethylphenoxy)-2,4-pyrimidinedione → 1-(Cyclobutylmethyl)-6-(3,5-dimethylphenoxy)-5-ethyl-pyrimidine-2,4-dione

HRID 1611263

Reaktionsgleichung

Reaktionsgleichung von HRID 1611263
[CH2:1]([C:3]1[C:4](=[O:19])[NH:5][C:6](=[O:18])[NH:7][C:8]=1[O:9][C:10]1[CH:15]=[C:14]([CH3:16])[CH:13]=[C:12]([CH3:17])[CH:11]=1)[CH3:2].C1(C)C=CC(S(O[CH2:30][CH:31]2[CH2:34][CH2:33][CH2:32]2)(=O)=O)=CC=1>>[CH:31]1([CH2:30][N:7]2[C:8]([O:9][C:10]3[CH:11]=[C:12]([CH3:17])[CH:13]=[C:14]([CH3:16])[CH:15]=3)=[C:3]([CH2:1][CH3:2])[C:4](=[O:19])[NH:5][C:6]2=[O:18])[CH2:34][CH2:33][CH2:32]1

Komponenten

3

Edukt 2

HCID 109232665-Ethyl-6-(3,5-dimethylphenoxy)-2,4-pyrimidinedioneHCID 13163931Cyclobutylmethyl 4-methylbenzenesulfonate

Produkt 1

HCID 99493421-(Cyclobutylmethyl)-6-(3,5-dimethylphenoxy)-5-ethyl-pyrimidine-2,4-dioneAusbeute 58,5 %

Versuchsvorschrift

5-Ethyl-6-(3,5-dimethylphenoxy)-2,4-pyrimidinedione and (cyclobutyl)methyl para-toluenesulfonate were reacted by the same way with the example 1 to obtain the titled compound (192 mg, yield: 58.5%).

Quellen und Nachweise

ORD-Eintrag
ord-9db64a969c444453be515a0d74a73ce1
Quelldatensatz
uspto-grants-2006_01
Patentnummer
US06987114B1

Verknüpfte Notizen

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