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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468628Generated: October 25, 2026

Iodine → N'-(Desmethyl)azithromycin

https://huagongshe.com/reaction/1468628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium HydroxideHCID 14923—
ReactantAzithromycinHCID 447043—
ReactantSodium AcetateHCID 517045—
ReactantDichloromethane methanol ammonium hydroxideHCID 21896990—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductN'-(Desmethyl)azithromycinHCID 998753355%

Reaction Conditions

Temperature50 °C

Reaction Steps

Azithromycin 1 (0.80 g, 1.02 mmol) and sodium acetate (NaOAc) (0.712 g, 8.06 mmol) were dissolved in 80% aqueous MeOH (25 mL). The solution was heated to 50° C. followed by addition of iodine (I2) (0.272 g, 1.07 mmol) in three batches within 3 minutes. The reaction was maintained at a pH between 8 and 9 by adding 1N sodium hydroxide (NaOH) (1 mL) at 10 min and 45 minute intervals. The solution turned colorless within 45 minutes. Stirring was continuedfor 2 hours. TLC (CH2Cl2/MeOH/NH4OH 10:1:0.05) after 2 hours showed a single major product (Rf=0.66). The reaction was cooled to room temperature, poured into H2O (75 mL) containing NH4OH (1.5 mL) and extracted with CHCl3 (3×30 mL). The combined organic layers were washed with H2O (30 mL) containing NH4OH (1.5 mL), dried over Na2SO4 and the solvent evaporated to give a white residue. The crude was purified on a silica gel column eluting with CH2Cl2/MeOH/NH4OH 18:1:0.05 to 10:1:0.05 to provide compound 2 (0.41 g, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006189B2
Source datasetuspto-grants-2015_04
ORD IDord-e364f484ab274094882462ae45f1e051
Source noteuspto-grants-2015_04