Carvedilol → Carvedilol
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:8]=1[O:9][CH2:10][CH2:11][NH:12][CH2:13][CH:14]([OH:30])[CH2:15][O:16][C:17]1[CH:18]=[CH:19][CH:20]=[C:21]2[NH:29][C:28]3[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=3[C:22]=12>CCCCCC.CC(O)C>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:8]=1[O:9][CH2:10][CH2:11][NH:12][CH2:13][CH:14]([OH:30])[CH2:15][O:16][C:17]1[CH:18]=[CH:19][CH:20]=[C:21]2[NH:29][C:28]3[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=3[C:22]=12.[CH3:1][O:2][C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:8]=1[O:9][CH2:10][CH2:11][NH2:12]Participants
4
Reactant 1
Product 2
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 55 °C
Procedure
Carvedilol (4 g) was dissolved in 180 ml, Hexane/IPA in a ratio 1:1 by heating the mixture under stirring at 55° C. water bath. The solution was allowed to sit at room temperature without stirring for about 15 h, then the resulting crystals were filtered through a buchner funnel and dried in a desiccator (connected to air pump) at room temperature until constant weight to yield Carvedilol Form III.
Workup
- temperatureby heating the mixture
- customto sit at room temperature
- stirringwithout stirring for about 15 h
- filtrationthe resulting crystals were filtered through a buchner funnel
- customdried in a desiccator (connected to air pump) at room temperature until constant weight
Sources & evidence
- ORD record
- ord-ca7b85da5cf243f8be9bf593565b53bb
- Source dataset
- uspto-grants-2004_03
- Patent number
- US06699997B2
Reaction notes
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