HCID 466690, compound → HCID 18925278, compound
Reaction equation
[CH2:1]([N:5]1[C:10]([S:11][C:12]2[CH:17]=[C:16]([CH3:18])[CH:15]=[C:14]([CH3:19])[CH:13]=2)=[C:9]([CH2:20][CH3:21])[C:8](=[O:22])[NH:7][C:6]1=[O:23])[CH:2]=[CH:3]C.C(N1C(SC2C=C(C)C=C(C)C=2)=C(CC)C(=O)NC1=O)C=CC1C=CC=CC=1.COC(C=CCN1C(SC2C=C(C)C=C(C)C=2)=C(CC)C(=O)NC1=O)=O.C(C=CCN1C(SC2C=C(C)C=C(C)C=2)=C(CC)C(=O)NC1=O)(O)=O.ClCC=CCN1C(SC2C=C(C)C=C(C)C=2)=C(CC)C(=O)NC1=O.C(N1C(SC2C=C(C)C=C(C)C=2)=C(CC)C(=O)NC1=O)C#C.C(N1C(SC2C=C(C)C=C(C)C=2)=C(CC)C(=O)NC1=O)C#CC.C1(C#CCN2C(SC3C=C(C)C=C(C)C=3)=C(CC)C(=O)NC2=O)C=CC=CC=1.C(N1C(SC2C=C(C)C=C(C)C=2)=C(CC)C(=O)NC1=O)C=CCC.OCC=CCN1C(SC2C=C(C)C=C(C)C=2)=C(CC)C(=O)NC1=O>>[CH2:1]([N:5]1[C:10]([S:11][C:12]2[CH:13]=[C:14]([CH3:19])[CH:15]=[C:16]([CH3:18])[CH:17]=2)=[C:9]([CH2:20][CH3:21])[C:8](=[O:22])[NH:7][C:6]1=[O:23])[CH:2]=[CH2:3]Participants
11
Reactant 10
Product 1
Procedure
1-(2-butenyl)-5-ethyl-6-(3,5-dimethylphenylthio)-2,4-pyrimidinedione; 1-cinnamyl-5-ethyl-6-(3,5-dimethylphenylthio)-2,4-pyrimidinedione; 1-(methoxycarbonylallyl)-5-ethyl-6-(3,5-dimethylphenylthio)-2,4-pyrimidinedione; 1-(carboxyallyl)-5-ethyl-6-(3,5-dimethylphenylthio)-2,4-pyrimidinedione; 1-(4-chloro-2-butenyl)-5-ethyl-6-(3,5-dimethylphenylthio)-2,4-pyrimidinedione; 1-propargyl-5-ethyl-6-(3,5-dimethylphenylthio)-2,4-pyrimidinedione; 1-(2-butynyl)-5-ethyl-6-(3,5-dimethylphenylthio)-2,4-pyrimidinedione; 1-(3-phenyl-2-propynyl)-5-ethyl-6-(3,5-dimethylphenylthio)-2,4-pyrimidinedione; 1-(2-pentenyl)-5-ethyl-6-(3,5-dimethylphenylthio)-2,4-pyrimidinedione; 1-(4-hydroxy-2-butenyl)-5-ethyl-6-(3,5-dimethylphenylthio)-2,4-pyrimidinedione;
Sources & evidence
- ORD record
- ord-702a945db79c4cda98fd5f2aea88804e
- Source dataset
- uspto-grants-1998_05
- Patent number
- US05747500
Reaction notes
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