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HRID 1356492作成日:2026年10月27日

Formic Acid → Azithromycin

https://huagongshe.com/reaction/1356492

反応式

関与物質

役割名称HCID仕込み量
反応物Formic AcidHCID 284—
反応物FormaldehydeHCID 712—
反応物WaterHCID 962—
反応物9-Deoxo-9a-aza-9a-homoerythromycin AHCID 9810601—
溶媒AcetoneHCID 180—
生成物AzithromycinHCID 447043—

反応条件

温度58 °C

反応手順

By the methods of the present invention, desmethyl-azithromycin is dissolved in acetone. Formaldehyde and formic acid are added to the solution and the clear solution is heated to reflux (˜58° C.). The mixture is maintained under reflux for about 3 hours then cooled to less than about 40° C. Water is added and the acetone is separated from the reaction mixture by distillation under low vacuum (˜300 mbar). The distillation is stopped when the temperature of the liquid phase reaches ˜40° C./300 mbar. Activated carbon SXI is added and the suspension is mixed for about 1 hour. The activated carbon is then separated from the solution by filtration on a Büchner filter containing Hyflow. The filter cake is washed with water. The pH is adjusted with an NaOH to about 10-10.5 to induce precipitation of azithromycin. The azithromycin suspension is stirred for about 1 hour. The crude azithromycin crude is separated by filtration and washed. Azithromycin is isolated upon drying the filtrate 40° C. in a vacuum oven. Preferably the azithromycin is dried for at least 24 hours. No impurities were detected that were derivatives of azithromycin in the isolated azithromycin Azithromycin dihydrate prepared in accordance with the present invention is suitable formulation and administration for the treatment of susceptible bacterial infections in humans according to the methods and in the amounts set forth in U.S. Pat. No. 4,474,768, cited above.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06586576B2
出典データセットuspto-grants-2003_07
ORD IDord-dd9974b1ba9e4539a3005f529b19fb00
出典メモuspto-grants-2003_07