HCID 86584629, compound → HCID 86584628, compound

HRID 430406Notes

Reaction equation

HRID 430406 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]2[C:13](=[O:14])[C:12](=[O:15])[CH:11](C)[NH:10]2)=[CH:5][CH:4]=1.COC1C=CC(N2C(=O)C(=O)C(C3C=CC=C(OC)C=3)N2)=CC=1.COC1C=CC(N2C(=O)C(=O)C(C3C=CC=CC=3)N2)=CC=1.COC1C=CC(N2C(=O)C(=O)C(C3C=CC(Cl)=CC=3)N2)=CC=1.COC1C=CC(N2C(=O)C(=O)C(C3C=CC(OC)=CC=3)N2)=CC=1.COC1C=CC(N2C(=O)C(=O)C(C3C=CC=C([N+]([O-])=O)C=3)N2)=CC=1.COC1C=CC(N2C(=O)C(=O)C(OC)N2)=CC=1.COC1C=CC(N2C(=O)C(=O)C(OCC)N2)=CC=1.COC1C=CC(N2C(=O)C(=O)C(N(C)C)N2)=CC=1.COC1C=CC(N2C(=O)C(=O)C(N(CC)CC)N2)=CC=1.COC1C=CC(N2C(=O)C(=O)C(NC(=O)C)N2)=CC=1.COC1C=CC(N2C(=O)C(=O)C(C(O)=O)N2)=CC=1.COC1C=CC(N2C(=O)C(=O)C(C(OC)=O)N2)=CC=1.COC1C=CC(N2C(=O)C(=O)C(C(OCC)=O)N2)=CC=1>>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([N:9]2[C:13](=[O:14])[C:12](=[O:15])[CH2:11][NH:10]2)=[CH:7][CH:8]=1

Participants

15

Procedure

1-(4′-methoxyphenyl)-3-methyl-4,5-pyrazolinedione; 1-(4′-methoxyphenyl) -3-(3′-methoxyphenyl)-4,5-pyrazolinedione; 1-(4′-methoxyphenyl)-3-phenyl-4,5-pyrazolinedione; 1-(4′-methoxyphenyl)-3-(4′-chlorophenyl)-4,5-pyrazolinedione; 1-(4′-methoxyphenyl)-3-(4′-methoxyphenyl)-4,5-pyrazolinedione; 1-(4′-methoxyphenyl)-3-(3′-nitrophenyl)-4,5-pyrazolinedione; 1-(4′-methoxyphenyl)-3-methoxy-4,5-pyrazolinedione; 1-(4′-methoxyphenyl)-3-ethoxy-4,5-pyrazolinedione; 1-(4′-methoxyphenyl)-3-dimethylamino-4,5-pyrazolinedione; 1-(4′-methoxyphenyl)-3-diethylamino-4,5-pyrazolinedione; 1-(4′-methoxyphenyl)-3-acetamido4,5-pyrazolinedione; 1-(4′-methoxyphenyl)-3-carboxy-4,5-pyrazolinedione; 1-(4′-methoxyphenyl)-3-methoxycarbonyl-4,5-pyrazolinedione; 1-(4′-methoxyphenyl)-3-ethoxycarbonyl-4,5-pyrazolinedione;

Sources & evidence

ORD record
ord-3106a99bd54c4b21ada04ba10d9f7f30
Source dataset
uspto-grants-2001_11
Patent number
US06322775B1

Reaction notes

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