Potassium Carbonate → HCID 13108891, compound
Reaction equation
Cl.Cl.[N:3]1([CH2:16][CH:17]([OH:35])[CH2:18][N:19]2[CH2:24][CH2:23][N:22]([CH2:25][CH2:26][CH2:27][S:28][C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=3)[CH2:21][CH2:20]2)[C:14](=[O:15])[C:13]2[N:11]([CH3:12])[CH:10]=[N:9][C:8]=2[N:6]([CH3:7])[C:4]1=[O:5].C(=O)([O-])[O-].[K+].[K+]>CCOCC>[N:3]1([CH2:16][CH:17]([OH:35])[CH2:18][N:19]2[CH2:20][CH2:21][N:22]([CH2:25][CH2:26][CH2:27][S:28][C:29]3[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=3)[CH2:23][CH2:24]2)[C:14](=[O:15])[C:13]2[N:11]([CH3:12])[CH:10]=[N:9][C:8]=2[N:6]([CH3:7])[C:4]1=[O:5]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
1.0 g of 1-(3-theobromin-1-yl-2-hydroxypropyl)-4-(3-phenylthiopropyl)piperazine 2 HCl suspended in 50 ml of ether is stirred with excess dilute aqueous potassium carbonate solution until the salt is completely dissolved. The organic layer is then separated, washed twice with water, dried over magnesium sulfate and evaporated to yield 1-(3-theobromin-1-yl-2-hydroxypropyl)-4-(3-phenylthiopropyl)piperazine as the free base.
Workup
- dissolutionis completely dissolved
- customThe organic layer is then separated
- washwashed twice with water
- dry with materialdried over magnesium sulfate
- customevaporated
Sources & evidence
- ORD record
- ord-0a352295890e4bbdb96c08a2dd119929
- Source dataset
- uspto-grants-1983_02
- Patent number
- US04374837
Reaction notes
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