참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Deferoxamine | HCID 2973 | — |
| 반응물 | Methanesulfonic Acid | HCID 6395 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | Deferoxamine Mesylate | HCID 62881 | — |
반응 단계
The deferoxamine free base was suspended in a 14:3 mixture of ethanol and water (42.5 L). Dilute methanesulfonic acid was slowly added to the suspension until the free base dissolved and the solution attained a pH of between 3.7 and 5. Ethanol (200 L) was added to the solution to precipitate the mesylate salt and the resulting suspension was cooled to −10° C. and maintained at −10° C. for several hours. The resulting crystals were isolated by filtration, washed with ethanol (50 L) and dried under vacuum to yield 3.4 kg of deferoxamine mesylate. HPLC chromatography showed that the mesylate contained 1.84 weight % impurities. The moisture content as determined by Karl-Fischer Analysis was 0.2 mole %. USP/NF 24/19, pp. 2003-2004 (1999). Coloration was better than Y5 as measured according to the European Pharmacopeia criteria for grading coloration.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06858414B2 |
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| 출처 데이터셋 | uspto-grants-2005_02 |
|---|
| ORD ID | ord-4842602b9ad14045b253873d24ba47c9 |
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| 출처 메모 | uspto-grants-2005_02 |
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