Citric Acid → HCID 86658825, compound
Reaction equation
[CH3:1][CH2:2][N:3]([CH2:6][CH2:7][NH:8][C:9]([C:11]1[C:12]([CH3:29])=[C:13](/[CH:17]=[C:18]2/[C:19]3[CH:20]=[C:21]([F:28])[CH:22]=[CH:23][C:24]=3[NH:25][C:26]/2=[O:27])[NH:14][C:15]=1[CH3:16])=[O:10])[CH2:4][CH3:5].[C:30]([OH:42])(=[O:41])[CH2:31][C:32]([CH2:37][C:38]([OH:40])=[O:39])([C:34]([OH:36])=[O:35])[OH:33]>CO>[CH3:1][CH2:2][N:3]([CH2:6][CH2:7][NH:8][C:9]([C:11]1[C:12]([CH3:29])=[C:13](/[CH:17]=[C:18]2/[C:19]3[CH:20]=[C:21]([F:28])[CH:22]=[CH:23][C:24]=3[NH:25][C:26]/2=[O:27])[NH:14][C:15]=1[CH3:16])=[O:10])[CH2:4][CH3:5].[C:30]([O-:42])(=[O:41])[CH2:31][C:32]([CH2:37][C:38]([O-:40])=[O:39])([C:34]([O-:36])=[O:35])[OH:33]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Sunitinib (2.21 g, 5.55 mmol) suspended in methanol (75 ml), 1.07 g of citric acid was added. Mixture was stirred at room temperature for several hours, and then filtered to obtain crystalline sunitinib citrate, 3.2 g. Melting point: 166-174° C. (Form I).
Workup
- filtrationfiltered
Sources & evidence
- ORD record
- ord-778ef29c63e241ab82928d8080f28ebb
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08686023B2
Reaction notes
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