HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → N-Desmethyl imatinib mesylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Cgp-74588 | HCID 9869737 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-Desmethyl imatinib mesylate | HCID 10188302 | — |
Reaction Steps
4.8 g (10 mmol) of N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-2-ylamino)-phenyl]-4-piperazin-1-ylmethyl-benzamide are dissolved in 20 ml of ethanol under heating and 0.99 g of methanesulfonic acid are added. After addition of ethyl acetate the product cristallizes. Drying at 50 mbar and 60° C. yields N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-2-ylamino)-phenyl]-4-piperazin-1-ylmethyl-benzamide methanesulfonate; Rf=0.17 (methylene chloride:ethyl acetate:methanol:conc. aqueous ammonium hydroxide solution=60:10:30:2); tR(HPLC)2) 14.6 min; m.p. 242-245° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07329661B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-c35b77c810504b82a25ea8e5e4054b91 |
| Source note | uspto-grants-2008_02 |