Reaction equation
C(O)(C)C.[CH3:5][C:6]1[CH:7]=[CH:8][C:9]([NH:25][C:26]([C:28]2[CH:29]=[CH:30][C:31]([CH2:34][N:35]3[CH2:40][CH2:39][N:38]([CH3:41])[CH2:37][CH2:36]3)=[CH:32][CH:33]=2)=[O:27])=[CH:10][C:11]=1[NH:12][C:13]1[N:14]=[CH:15][CH:16]=[C:17]([C:19]2[CH:20]=[CH:21][CH:22]=[N:23][CH:24]=2)[N:18]=1.[CH3:42][S:43]([OH:46])(=[O:45])=[O:44]>O>[CH3:5][C:6]1[CH:7]=[CH:8][C:9]([NH:25][C:26]([C:28]2[CH:33]=[CH:32][C:31]([CH2:34][N:35]3[CH2:36][CH2:37][N:38]([CH3:41])[CH2:39][CH2:40]3)=[CH:30][CH:29]=2)=[O:27])=[CH:10][C:11]=1[NH:12][C:13]1[N:14]=[CH:15][CH:16]=[C:17]([C:19]2[CH:20]=[CH:21][CH:22]=[N:23][CH:24]=2)[N:18]=1.[CH3:42][S:43]([OH:46])(=[O:45])=[O:44]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The solution of imatinib mesylate and isopropanol is prepared by a process comprising: providing a suspension of imatinib base and isopropanol containing up to 7% by weight of water; admixing the suspension with cooled methanesulfonic acid; and maintaining the mixture at the cooled temperature to obtain a solution of imatinib mesylate. Preferably, the suspension of imatinib base is prepared by suspending imatinib base in isopropanol containing up to 7% by weight of water at a temperature of about −10° C. to about −5° C., more preferably, at a temperature of about −10° C. Preferably, the isopropanol contains up to 5% of water by weight. Preferably, methanesulfonic acid is added to the suspension at a temperature of about 0° C. to about −10° C., more preferably at a temperature of about −10° C., most preferably in a stoichiometric amount. Preferably, the solution is maintained at a temperature of about 0° C. to about −20° C., more preferably, at a temperature of about −15° C. Preferably, the solution is maintained for a period of about 10 hours to about 24 hours, more preferably for about 12 hours to about 16 hours, most preferably about 12 hours.
Workup
- customproviding
- temperatureand maintaining the mixture at the cooled temperature
Sources & evidence
- ORD record
- ord-1ff0e65533fe4bca87e11e04a16be38f
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08067421B2
Linked notes
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