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HRID 505833作成日:2026年10月23日

Kanamycin A Sulfate → (2S,3R,4R,5S,6S)-2-(aminomethyl)-6-[(1R,2R,3S,4R,6S)-4,6-diamino-3-[(2S,3R,4S,5S,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-hydroxycyclohexyl]oxyoxane-3,4,5-triol

https://huagongshe.com/ja/reaction/505833

反応式

関与物質

役割名称HCID仕込み量
反応物Kanamycin A SulfateHCID 441374—
溶媒WaterHCID 962—
生成物(2S,3R,4R,5S,6S)-2-(aminomethyl)-6-[(1R,2R,3S,4R,6S)-4,6-diamino-3-[(2S,3R,4S,5S,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-hydroxycyclohexyl]oxyoxane-3,4,5-triolHCID 11274101113.6%

反応手順

Kanamycin sulfate (20.0 g) was dissolved in 200 mL of water. This was loaded on a column prepared with 400 g of AMBERLITE IRA-140 resin (6.4 cm×17.5 cm). The column was eluted with water, and the appropriate fractions were collected and lyophilized to give 18.9 g of kanamycin A (free base) (18).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07781570B2
出典データセットuspto-grants-2010_08
ORD IDord-475ee180131f46c7bdd3e9346254273f
出典メモuspto-grants-2010_08