AN ARYLATION METHOD FOR THE FUNCTIONALIZATION OF O-ALLYL ERYTHROMYCIN DERIVATIVES
Application 1095/MUMNP/2003 published 2006-07-28, filed 2003-11-27
An efficient arylation technique for use in the synthesis of erythromycin derivatives, involving a modified Heck reaction which employs less than six mole percent of palladium catalyst and no phosphine is disclosed. With this modified Heck reaction, an O-alkenylaryl macrolide can be obtained in a much shorter reaction time than under conventional Heck reaction conditions. The modified Heck reaction can be utilized in a method for phosphine-free arylation of an O-allylic erythromycin derivative, in a method for preparing an O-alkenylaryl erythromycin A derivative, or in a method for preparing a 2', 4"-hydroxyl protected 6-O-alkenylaryl erythromycin A derivative. Drawing: Sheets Total Pages: Fig.
Applicant
ABBOTT LABORATORIES
D-377 AP6D, 100 ABBOTT PARK ROAD, ABBOTT PARK, IL 60064-6050, U.S.A.
Inventor
1. ZHANG WEIJIANG 2. HSU MARGARET CHI-PING 3. HAIGHT ANTHONY 4. PETERSON MATTHEW JOHN 5. NARAYANAN BIKSHANDARKOIL
International Info
Classification: C07H 17/08
Publication Number: WO 02/096922
Application Date: 2002-05-21
Priority Information
60/294,326 U.S.A. 2001-05-30