HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imatinib → Imatinib Mesylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imatinib | HCID 5291 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Solvent | 1,3-Dioxolane | HCID 12586 | — |
| Product | Imatinib Mesylate | HCID 123596 | — |
Reaction Steps
Imatinib base (1 g) was suspended in aqueous 1,3-dioxolane (5 ml, 10% of water, v/v) at 15° C. Methanesulfonic acid (0.125 ml) was added obtaining the solution of imatinib mesylate. The solution thus formed was cool down to about 10° C. and additional portion of 1,3-dioxolane (15 ml) was added into the mixture. The suspension was stirred at 5° C. for 10 min and the white solid was filtered, washed with 1,3-dioxolane, and the solid matter was dried at 25° C. under N2 flow for 4 h to obtain imatinib mesylate Form VI (0.6 g, yield: 50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977348B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-f2af5c9ea64e459eaf1dbfaab4e89e32 |
| Source note | uspto-grants-2011_07 |