HCID 67566857, compound → HCID 86584612, compound

HRID 430404Notes

Reaction equation

HRID 430404 reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:12](=[O:13])[C:11](=[O:14])[CH:10](C)[NH:9]2)=[CH:4][CH:3]=1.CC1C=CC(N2C(=O)C(=O)C(C3C=CC=CC=3)N2)=CC=1.CC1C=CC(N2C(=O)C(=O)C(C3C=CC(Cl)=CC=3)N2)=CC=1.CC1C=CC(N2C(=O)C(=O)C(C3C=CC=C(OC)C=3)N2)=CC=1.CC1C=CC(N2C(=O)C(=O)C(C3C=CC(OC)=CC=3)N2)=CC=1.CC1C=CC(N2C(=O)C(=O)C(C3C=CC=C([N+]([O-])=O)C=3)N2)=CC=1.CC1C=CC(N2C(=O)C(=O)C(C3C=CC(C)=CC=3)N2)=CC=1.CC1C=CC(N2C(=O)C(=O)C(OC)N2)=CC=1.CC1C=CC(N2C(=O)C(=O)C(OCC)N2)=CC=1.CC1C=CC(N2C(=O)C(=O)C(N(C)C)N2)=CC=1.CC1C=CC(N2C(=O)C(=O)C(N(CC)CC)N2)=CC=1.CC1C=CC(N2C(=O)C(=O)C(NC(=O)C)N2)=CC=1.CC1C=CC(N2C(=O)C(=O)C(C(O)=O)N2)=CC=1.CC1C=CC(N2C(=O)C(=O)C(C(OC)=O)N2)=CC=1.CC1C=CC(N2C(=O)C(=O)C(C(OCC)=O)N2)=CC=1>>[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[C:12](=[O:13])[C:11](=[O:14])[CH2:10][NH:9]2)=[CH:6][CH:7]=1

Participants

16

Procedure

1-(4′-methylphenyl)-3-methyl-4,5-pyrazolinedione; 1-(4′-methylphenyl)-3-phenyl-4,5-pyrazolinedione; 1-(4′-methylphenyl)-3-(4′-chlorophenyl)-4,5-pyrazolinedione; 1-(4′-methylphenyl)-3-(3′-methoxyphenyl)-4,5-pyrazolinedione; 1-(4′-methylphenyl)-3-(4′-methoxyphenyl)-4,5-pyrazolinedione; 1-(4′-methylphenyl)-3-(3′-nitrophenyl)-4,5-pyrazolinedione; 1-(4′-methylphenyl)-3-(4′-methylphenyl)-4,5-pyrazolinedione; 1-(4′-methylphenyl)-3-(2′-furyl)-4,5-pyrazolinedione; 1-(4′-methylphenyl)-3-(2′-thienyl)-4,5-pyrazolinedione; 1-(4′-methylphenyl)-3-(5′-pyrazolyl)-4,5-pyrazolinedione; 1-(4′-methylphenyl)-3-methoxy-4,5-pyrazolinedione; 1-(4′-methylphenyl)-3-ethoxy-4,5-pyrazolinedione; 1-(4′-methylphenyl)-3-dimethylamino-4,5-pyrazolinedione; 1-(4-methylphenyl)-3-diethylamino-4,5-pyrazolinedione; 1-(4′-methylphenyl)-3-acetamido-4,5-pyrazolinedione; 1-(4′-methylphenyl)-3-carboxy-4,5-pyrazolinedione; 1-(4′-methylphenyl)-3-methoxycarbonyl-4,5-pyrazolinedione; 1-(4′-methylphenyl)-3-ethoxycarbonyl-4,5-pyrazolinedione;

Sources & evidence

ORD record
ord-db51a9a36ad84a44b7210053e61748b9
Source dataset
uspto-grants-2001_11
Patent number
US06322775B1

Reaction notes

Loading…