Chinese Journal of Applied Chemistry ›› 2011, Vol. 28 ›› Issue (03): 263-266.DOI: 10.3724/SP.J.1095.2011.00327

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N-Alkylations of Two Indole Derivatives

MA Wenkang, LU Xingping, HUANG Yan*, LUO Jiandong*   

  1. (Department of Foundation,Guangzhou Medical College,Guangzhou  510182)
  • Received:2010-06-07 Revised:2010-07-22 Published:2011-03-10 Online:2011-03-10

Abstract:

The N-alkylations of methyl 3-indoleglyoxylate and indole-3-acetonitrile were carried out using alkyl halides or sulfonates as electrophiles in the presence of bases and six new N-alkylation products of indole derivatives were prepared. The influences of the structures of indole derivatives and electrophiles, the solvents and bases on the alkylations have been studied. The N-alkylation of methyl 3-indoleglyoxylate with a strong electron-withdrawing group could be conducted using weak base Cs2CO3 in mild reaction condition and in 93% yields while a strong base such as NaH must be used when indole-3-acetonitrile with a weak electron-withdrawing group was used as reactant in the N-alkylation.

Key words: indole derivatives, N-alkylation, synthesis

CLC Number: