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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 219519생성일: 2026년 10월 26일

Iodine → N'-(Desmethyl)azithromycin

https://huagongshe.com/reaction/219519

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참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Sodium HydroxideHCID 14798—
반응물Ammonium HydroxideHCID 14923—
반응물AzithromycinHCID 447043—
반응물Sodium AcetateHCID 517045—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물N'-(Desmethyl)azithromycinHCID 998753355%

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온도50 °C

반응 단계

Azithromycin 1 (0.80 grams (g), 1.02 millimoles (mmol)) and sodium acetate (NaOAc) (0.712 g, 8.06 mmol) were dissolved in 80% aqueous methanol (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 8-9 by adding 1N sodium hydroxide (NaOH) (1 mL) at 10 min and 45 minute intervals. The solution turned colorless within 45 minutes (min), however, stirring was continued for 2 hours (hr). TLC ethylene chloride(CH2Cl2)/MeOH/ammonium chloride (NH4OH) 10:1:0.05) after 2 hours showed a single major product (Rf=0.66). The reaction was cooled to room temperature (rt), poured into H2O (75 mL) containing NH4OH (1.5 mL) and extracted with chloroform (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 amine 2 (0.41 g, 55%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202843B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-5b59680f52a1401cba133b736464bb7a
출처 메모uspto-grants-2012_06