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 1,3-dioxolane (4.5 ml) at 15° C. Aqueous methanesulfonic acid (0.125 ml in 0.5 ml of water) 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 3 h, providing form VI. The white solid was filtered, washed with 1,3-dioxolane, and the solid matter was dried first for 6 h at RT and than for 6 h at 60° C. under flow of nitrogen to obtain imatinib mesylate Form V (1.0 g, yield: 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977348B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-7f25c4dbde5741818d383d3eacd36fd2 |
| Source note | uspto-grants-2011_07 |