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Deferoxamine → Deferoxamine Mesylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Deferoxamine | HCID 2973 | — |
| 反応物 | Methanesulfonic Acid | HCID 6395 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | Deferoxamine Mesylate | HCID 62881 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06858414B2 |
| 出典データセット | uspto-grants-2005_02 |
| ORD ID | ord-0224a31cbf1f4feab1a91519dee50bfe |
| 出典メモ | uspto-grants-2005_02 |