Hydrochloric Acid → HCID 53628934, compound
Reaction equation
[ClH:1].[CH3:2][O:3][C:4]1[CH:9]=[CH:8][C:7]([CH:10]2[CH2:15][N:14]([C:16]3[N:21]([CH3:22])[C:20](=[O:23])[CH:19]=[C:18]([C:24]4[CH:29]=[CH:28][N:27]=[CH:26][CH:25]=4)[N:17]=3)[CH2:13][CH2:12][NH:11]2)=[CH:6][CH:5]=1>C(OCC)(=O)C.ClCCl>[ClH:1].[ClH:1].[CH3:2][O:3][C:4]1[CH:5]=[CH:6][C:7]([CH:10]2[CH2:15][N:14]([C:16]3[N:21]([CH3:22])[C:20](=[O:23])[CH:19]=[C:18]([C:24]4[CH:25]=[CH:26][N:27]=[CH:28][CH:29]=4)[N:17]=3)[CH2:13][CH2:12][NH:11]2)=[CH:8][CH:9]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
4N Hydrogen chloride in ethyl acetate (5 ml) was added to the solution of 2-(2-(4-methoxyphenyl)-piperazine-4-yl)-3-methyl-6-(4-pyridyl)pyrimidin-4-one (594 mg, 1.6 mmol) in dichloromethane (5 ml) and stirred for 1 hr. Wash with ethyl acetate after removal of the solvent and dryness gave the title compound (683 mg, 96%).
Workup
- washWash with ethyl acetate
- customafter removal of the solvent and dryness
Sources & evidence
- ORD record
- ord-1cc5ded6a9224a0f953c34488890b846
- Source dataset
- uspto-grants-2009_03
- Patent number
- US07504411B2
Reaction notes
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