Hydrochloric Acid → HCID 21254478, compound
Reaction equation
C(O)(=O)/C=C/C(O)=O.[NH:9]1[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]1.[ClH:15]>C(O)C>[ClH:15].[ClH:15].[ClH:15].[NH:9]1[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
5 g of 1-diphenylmethyl-4-[2-(-4-methylphenyl)-5-methyl-1H-imidazol-4-yl)methyl]piperazine monofumarate were dissolved in 100 ml of hot ethanol. 3 ml of commercial concentrated HCl solution (10N) were added with stirring. The solution was refluxed for 30 minutes then the solution was allowed to cool to room temperature. The solvent was evaporated off and the residue was crystallized twice from ethanol at 98° C. to yield 1-diphenylmethyl-4-[2-(-4-methylphenyl)-5-methyl-1H-imidazol-4-yl)methyl]piperazine trihydrochloride, m.p. 202°-204° with decomposition.
Workup
- temperatureThe solution was refluxed for 30 minutes
- customThe solvent was evaporated off
- customthe residue was crystallized twice from ethanol at 98° C.
Sources & evidence
- ORD record
- ord-fa243c314dcc4ec1897eea3c1de5bba4
- Source dataset
- uspto-grants-1991_08
- Patent number
- US05043447
Reaction notes
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