Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imatinib | HCID 5291 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 1-Methoxyethanol | HCID 3015637 | — |
| Reactant | 1-Ethoxyethanol | HCID 10129898 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Nitromethane | HCID 6375 | — |
| Solvent | Propylene Carbonate | HCID 7924 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | Imatinib Mesylate | HCID 123596 | — |
Reaction Steps
Alternatively, the solution may be prepared by admixing imatinib base, methanesulfonic acid and a solvent selected from the group consisting of: methanol, methoxyethanol or ethoxyethanol, N-methylpyrrolidone, propylene carbonate, acetonitrile, nitromethane to obtain a mixture; and heating the mixture to obtain an imatinib mesylate solution. Heating the mixture to obtain an imatinib mesylate solution is preferably to a temperature of about 20° C. to about 85° C., more preferably of about 60° C. to about 80° C. Preferably, the obtained solution is further cooled to a temperature of about 20° C. to about 0° C. prior to the addition of the anti-solvent. Preferably the solution of imatinib mesylate is gradually added to the anti-solvent under stirring. Preferably, the solution of imatinib mesylate is added to an excess of anti-solvent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08067421B2 |
|---|
| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-c47d0b859c424b8288f13b2b12baf475 |
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| Source note | uspto-grants-2011_11 |
|---|