Hydrochloric Acid → HCID 22388387, compound
Reaction equation
[C:1]([N:4]([CH2:17][C:18]1[CH:23]=[CH:22][C:21]([Cl:24])=[CH:20][C:19]=1[Cl:25])[C:5]1[CH:10]=[C:9]([C:11](=[O:13])[NH2:12])[CH:8]=[CH:7][C:6]=1[C:14](=[O:16])[NH2:15])(=O)[CH3:2].Cl>CO>[C:11]([C:9]1[CH:10]=[C:5]2[C:6]([C:14](=[O:16])[N:15]=[C:1]([CH3:2])[N:4]2[CH2:17][C:18]2[CH:23]=[CH:22][C:21]([Cl:24])=[CH:20][C:19]=2[Cl:25])=[CH:7][CH:8]=1)(=[O:13])[NH2:12]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2-((N-Acetyl)-(2,4-dichlorobenzyl)amino)-1,4-dicarbamoylbenzene (1.50 g) in a mixture of concentrated hydrochloric acid (10 ml) and methanol (30 ml) was heated under reflux for 30 min. After concentration, the object compound (1.46 g) was obtained as white crystals.
Workup
- temperaturewas heated
- temperatureunder reflux for 30 min
- concentrationAfter concentration
Sources & evidence
- ORD record
- ord-9a62b363fd0f4b809f6535a3a6b42d4c
- Source dataset
- uspto-grants-2002_02
- Patent number
- US06348474B1
Reaction notes
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