Hydrochloric Acid → HCID 67450266, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[N:9]([CH2:25][CH2:26][S:27]([CH3:30])(=[O:29])=[O:28])[C:10]2[C:15]([N:16]=1)=[C:14]([N:17]1[CH2:22][CH2:21][N:20]([CH3:23])[CH2:19][CH2:18]1)[N:13]=[C:12]([CH3:24])[N:11]=2.Cl>C(O)C>[ClH:1].[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[N:9]([CH2:25][CH2:26][S:27]([CH3:30])(=[O:29])=[O:28])[C:10]2[C:15]([N:16]=1)=[C:14]([N:17]1[CH2:22][CH2:21][N:20]([CH3:23])[CH2:19][CH2:18]1)[N:13]=[C:12]([CH3:24])[N:11]=2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Suspend 8-(2-chlorophenyl)-2-methyl-6-(4-methylpiperazin-1-yl)-9-(2-methylsulfonylethyl)purine (11.3 g, 25.2 mmol) in ethanol (150 mL) and add 1 N aqueous hydrogen chloride solution (6.29 mL, 25.2 mmol, 1 eq). Allow the mixture to stir overnight and concentrate under reduced pressure. Collect the precipitated solids by filtration, wash with acetone, and dry under vacuum to afford the title compound (10.6 g). ES/MS m/z 449 (M+1).
Workup
- concentrationconcentrate under reduced pressure
- customCollect the precipitated solids
- filtrationby filtration
- washwash with acetone
- customdry under vacuum
Sources & evidence
- ORD record
- ord-a6cff83892564ae4ba733b8314cf25d1
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08710063B2
Reaction notes
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