Piperazine → HCID 70480299, compound

HRID 1197463Notes

Reaction equation

HRID 1197463 reaction equation
[NH:1]1[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.[C:7]([OH:14])(=[O:13])/[CH:8]=[CH:9]\[C:10]([OH:12])=[O:11]>C(O)C>[C:7]([OH:14])(=[O:13])/[CH:8]=[CH:9]\[C:10]([OH:12])=[O:11].[NH:1]1[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1

Participants

4

Reactant 2

HCID 4837PiperazineHCID 444266Maleic Acid

Product 1

HCID 70480299HCID 70480299, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

Monomaleate salt--5 g. (0.0115 mole) of 1-diphenylmethyl-4-[2-(-4-methylphenyl)-5-methyl-1H-imidazol-4-yl)-methyl]piperazine were dissolved in 300 ml of ethanol at 95° C. To this solution 1.34 g (0.0115 mole) of maleic acid was added with stirring. The reaction mixture was stirred at room temperature for 2 hours then the solvents were evaporated off under reduced pressure. The residue was dissolved in ether and the precipitate was filtered. The precipitate was recrystallized from isopropyl ether:acetone (1:1) to yield 1-diphenylmethyl-4-[2-(-4-methylphenyl)-5-methyl-1H-imidazol-4-yl)-methyl]piperazine monomaleate. m.p. 164°-166° C. with decomposition.

Workup

  1. stirringThe reaction mixture was stirred at room temperature for 2 hours
  2. customthe solvents were evaporated off under reduced pressure
  3. dissolutionThe residue was dissolved in ether
  4. filtrationthe precipitate was filtered
  5. customThe precipitate was recrystallized from isopropyl ether:acetone (1:1)

Sources & evidence

ORD record
ord-71ba74a47e1a43428bdd236b9fd15e42
Source dataset
uspto-grants-1994_01
Patent number
US05276034

Reaction notes

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