Ammonia → HCID 178428281, compound

HRID 729188Notes

Reaction equation

HRID 729188 reaction equation
CS(O)(=O)=O.[NH2:6][C:7]1[C:15](=[O:16])[N:10]2[CH2:11][CH2:12][CH2:13][CH2:14][N:9]2[C:8]=1[NH2:17].[NH2:18][C:19]1[C:20]([Cl:27])=[C:21]([OH:26])[C:22]([CH3:25])=[CH:23][CH:24]=1.N.OO>O.C(O)C>[NH2:17][C:8]1[N:9]2[CH2:14][CH2:13][CH2:12][CH2:11][N:10]2[C:15](=[O:16])[C:7]=1[N:6]=[C:24]1[CH:23]=[C:22]([CH3:25])[C:21](=[O:26])[C:20]([Cl:27])=[C:19]1[NH2:18]

Participants

7

Reactant 4

HCID 222AmmoniaHCID 784Hydrogen PeroxideHCID 1576415-Amino-6-Chloro-o-CresolHCID 86627737HCID 86627737, compound

Product 1

HCID 178428281HCID 178428281, compound

Reagents, catalysts & solvents 2

HCID 702EthanolSolventHCID 962WaterSolvent

Procedure

0.68 mmol of 2,3-diamino-5,6,7,8-tetrahydro-1H-pyrazolo[1,2-a]pyridazin-1-one methanesulfonate was dissolved in a mixture of water and ethanol (7.5 ml/1.5 ml). This solution was admixed with 0.68 mmol of 3-amino-2-chloro-6-methylphenol, then with 1.8 ml of concentrated aqueous ammonia, then with 9 ml of hydrogen peroxide.

Sources & evidence

ORD record
ord-e92e10d6aa1a4cfe913c677bdf96f2bf
Source dataset
uspto-grants-2009_09
Patent number
US07582123B2

Reaction notes

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