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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402208Generated: October 23, 2026

Amikacin Sulfate Salt → Amikacin

https://huagongshe.com/en/reaction/402208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmikacin Sulfate SaltHCID 5458175—
SolventWaterHCID 962—
ProductAmikacinHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742078B2
Source datasetuspto-grants-2014_06
ORD IDord-3d062aab620c4a33ae99c0adb41a3687
Source noteuspto-grants-2014_06