Hydrochloric Acid → HCID 21497124, compound
Reaction equation
[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6]([NH:12][C:13]3[CH:28]=[CH:27][C:16]([C:17]([N:19]4[CH2:24][CH2:23][N+:22]([O-:26])([CH3:25])[CH2:21][CH2:20]4)=[O:18])=[CH:15][CH:14]=3)=[CH:7][CH:8]=[N:9]2)=[CH:4][CH:3]=1.[ClH:29]>C(O)C>[ClH:1].[ClH:29].[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6]([NH:12][C:13]3[CH:28]=[CH:27][C:16]([C:17]([N:19]4[CH2:20][CH2:21][N+:22]([O-:26])([CH3:25])[CH2:23][CH2:24]4)=[O:18])=[CH:15][CH:14]=3)=[CH:7][CH:8]=[N:9]2)=[CH:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
1-[p-[(7-chloro-4-quinolyl)amino]benzoyl]-4-methylpiperazine-4-oxide (Example 1, supra.) and a mixture of hydrochloric acid in ethanol are admixed together, in proportions such that the molar proportion of acid istwice the molar proportion of the oxide reactant. The reaction mixture is evaporated to dryness under reduced atmospheric pressure and the residue recrystallized from ethanol to give 1-[p-[(7-chloro-4-quinolyl)amino]benzoyl]-4-methylpiperazine-4-oxide dihydrochloride.
Workup
- customThe reaction mixture is evaporated to dryness under reduced atmospheric pressure
- customthe residue recrystallized from ethanol
Sources & evidence
- ORD record
- ord-eb67b9c6d170464087504bf3a00e38e6
- Source dataset
- uspto-grants-1976_11
- Patent number
- US03992382
Reaction notes
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