Erythromycin derivatives as antibacterial agents
A technology of solvates and halogens, applied in the field of new antibiotics, can solve the problems of not having a direct bonded benzene ring, not disclosing, etc.
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[0144] 4″-O-(allyloxycarbonyl)-N-demethyl clarithromycin 11,12-carbonate-2′,3′-aminomethyl Ethyl acetate (5)
[0145] Clarithromycin (4, 5.00 g, 6.69 mmol) was dissolved in dichloromethane (100 mL), and pyridine (6.30 mL, 77.9 mmol) and phosgene (20.0 mL, 38.0 mmol in 20% toluene) were added. The reaction mixture was stirred at room temperature for 5 hours. Allyl alcohol (9.00ml, 132mmol) was added and stirring continued for an additional 30 minutes (yellow solution). Aqueous sodium hydroxide solution was added, and the product was extracted with dichloromethane. The combined organic layers were washed with water and brine, dried over magnesium sulfate and filtered. Evaporation of the filtrate and chasing toluene gave a pale yellow solid which was recrystallized from toluene; 5.07 g (87%) of allyl carbonate 5 was obtained as a white solid; mp.: 307-310° C. (toluene). (C 43 h 67 NO 17 Calculated: C, 59.36; H, 7.76. Found: C, 60.01; H, 7.36%). HRMS, ESIpos.: M+Na + =...
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