Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Amikacin Sulfate Salt | HCID 5458175 | — |
| Solvent | Water | HCID 962 | — |
| Product | Amikacin | HCID 37768 | — |
Reaction Steps
Amikacin sulfate 1.0 grams (Commercially available from a number of chemical companies: O. M. Chemical Co., Ltd., Shanghai, China; Zhejiang Winsun Imp. & Exp. Co., Ltd, Zhejiang, China; Ningbo DHY Pharmaceutical Co., Zhejiang, China; and Shanghai Xudong Haipu Pharmaceutical Co., Ltd, Shanghai, China) was treated with 4 grams of Amberlite ion exchange resin (OH— form, Aldrich, Milwaukee, Wi) in 10 mL of water for 1 hour. The resultant solution was filtered and lyophilized to give Amikacin Free Base. The Amikacin free base (5.0 g, 8.5 mmoles) was dissolved in a mixture of 1,4-dioxane (165 mL) and H2O (235 mL). To this solution was added tert-butyloxycarbonyloxy-5-norbornene-2,3-dicarboxamide (1.3 g, 7.8 mmoles) dissolved in a mixture of CH2Cl2 (10 mL) and 1,4-dioxane (5 mL), over 50 min at room temperature. The reaction was stirred at room temp for 3 hours, and then evaporated under reduced pressure. The resultant solid was subjected to silica gel chromatography (4:4:2, MeOH, CH2Cl2, NH4OH, Rf=0.25) and then lyophilized to give the title compound, 1.6 g (30%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08742078B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-3d062aab620c4a33ae99c0adb41a3687 |
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| Source note | uspto-grants-2014_06 |
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