Phosphoric Acid → HCID 131734274, 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].[P:30](=[O:34])([OH:33])([OH:32])[OH:31]>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].[P:30]([O-:34])([O-:33])([O-:32])=[O:31]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 30 °C
Procedure
Sunitinib (1.0 g) was suspended in methanol (152 mL), followed by addition of phosphoric acid (0.24 g) at 25-35° C. over a period of 15 minutes. After the stipulated time period, methanol was completely distilled off under vacuum below 45° C. The residue was treated with acetonitrile (38 mL) and refluxed. The reaction mass was maintained at reflux temperature for 60 minutes. The reaction mass was cooled to 25-35° C. for crystallization. The solid obtained was filtered, washed with acetonitrile, suck dried and dried under vacuum at 60° C. over 4-5 hr period to obtain sunitinib phosphate. (1.18 g; yield: 95%)
Workup
- distillationAfter the stipulated time period, methanol was completely distilled off under vacuum below 45° C
- additionThe residue was treated with acetonitrile (38 mL)
- temperaturerefluxed
- temperatureThe reaction mass was maintained
- temperatureat reflux temperature for 60 minutes
- customThe solid obtained
- filtrationwas filtered
- washwashed with acetonitrile, suck
- customdried
- customdried under vacuum at 60° C. over 4-5 hr period
Sources & evidence
- ORD record
- ord-59f322c27c104d96a44c58c630d52bc6
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09206163B2
Reaction notes
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