2,4-Diaminotoluene → HCID 178428252, compound

HRID 729198

Reaction equation

HRID 729198 reaction equation
[CH3:1][N:2]1[C:6]([CH3:7])=[C:5]([N:8]=O)[C:4](=[O:10])[N:3]1[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.[CH3:17][C:18]1[CH:23]=[CH:22][C:21]([NH2:24])=[CH:20][C:19]=1[NH2:25].[Cl:26]([O-:30])(=[O:29])(=[O:28])=[O:27].[Na+]>C(O)(=O)C.O>[Cl:26]([O-:30])(=[O:29])(=[O:28])=[O:27].[NH2:24][C:21]1/[C:22](=[N:8]/[C:5]2[C:4](=[O:10])[N:3]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)[N:2]([CH3:1])[C:6]=2[CH3:7])/[CH:23]=[C:18]([CH3:17])[C:19](=[NH2+:25])[CH:20]=1

Participants

6

Procedure

50 mmol of 1,5-dimethyl-4-nitroso-2-phenyl-1,2-dihydro-3H-pyrazol-3-one was dissolved in a solution of 850 ml of acetic acid and 1250 ml of water. This solution was admixed with 50 mmol of 4-methylbenzene-1,3-diamine and stirring was continued for 2 h 30 min. 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
  2. waitto stand for 30 minutes at zero degrees

Sources & evidence

ORD record
ord-337954db342c466cbcef6fe9888bb754
Source dataset
uspto-grants-2009_09
Patent number
US07582123B2

Linked notes

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