4-Aminoantipyrine → HCID 178429953, compound

HRID 729197Notes

Reaction equation

HRID 729197 reaction equation
[NH2:1][C:2]1[C:3](=[O:15])[N:4]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[N:5]([CH3:8])[C:6]=1[CH3:7].[CH3:16][N:17]([CH3:25])[C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([NH2:24])[CH:19]=1.[Cl:26]([O-:30])(=[O:29])(=[O:28])=[O:27].[Na+]>[Cl-].[Na+]>[Cl:26]([O-:30])(=[O:29])(=[O:28])=[O:27].[NH2:24][C:20]1=[CH:19][C:18](=[N+:17]([CH3:25])[CH3:16])[CH:23]=[CH:22]/[C:21]/1=[N:1]\[C:2]1[C:3](=[O:15])[N:4]([C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=2)[N:5]([CH3:8])[C:6]=1[CH3:7]

Participants

5

Procedure

60 mmol of 4-amino-1,5-dimethyl-2-phenyl-1,2-dihydro-3H-pyrazol-3-one and 60 mmol of N,N-dimethylbenzene-1,3-diamine was dissolved in 300 ml of ice-water. This solution was admixed with 60 mmol of ferric chloride and 300 ml of saturated aqueous sodium chloride. Sodium perchlorate was added to saturation, and the mixture was left to stand for 30 minutes at zero degrees.

Workup

  1. waitthe mixture was left

Sources & evidence

ORD record
ord-b7ea82bc5e1644449e81da90f5b5dfc2
Source dataset
uspto-grants-2009_09
Patent number
US07582123B2

Reaction notes

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