HuagongsheHuagongshe Chemistry Print Report · For research reference only
Deferoxamine → Deferoxamine Mesylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Deferoxamine | HCID 2973 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | Deferoxamine Mesylate | HCID 62881 | — |
Reaction Steps
The deferoxamine B base was then suspended in a mixture of ethanol (3.1 L) and water (0.46 L). Methanesulfonic acid was slowly added until the deferoxamine B base dissolved and the solution reached a pH of 3.5. Another 30 L of ethanol was added to the solution to precipitate deferoxamine B mesylate. The resulting suspension was then cooled to between −5° C. and 0° C. and maintained at reduced temperature for 24 h. The crystals were isolated by filtration, washed with ethanol and dried under vacuum to yield deferoxamine B mesylate (299 g) with a purity of 98% (w/w) as determined by HPLC analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06858414B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-0224a31cbf1f4feab1a91519dee50bfe |
| Source note | uspto-grants-2005_02 |