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HRID 388198作成日:2026年10月27日

Amikacin Sulfate Salt → Amikacin

https://huagongshe.com/reaction/388198

反応式

関与物質

役割名称HCID仕込み量
反応物Amikacin Sulfate SaltHCID 5458175—
溶媒WaterHCID 962—
生成物AmikacinHCID 37768—

反応手順

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, Wis.) 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08377896B2
出典データセットuspto-grants-2013_02
ORD IDord-b7ff72f6b48f46debd8dcb5898fdd60a
出典メモuspto-grants-2013_02