Direct amidation of poly(gamma-glutamic acid) with benzylamine in dimethyl sulfoxide

Biomacromolecules. 2007 May;8(5):1624-32. doi: 10.1021/bm0612182. Epub 2007 Apr 20.

Abstract

Partially benzylamidated, amphipathic poly(gamma-glutamic acid) (BzPGA) was synthesized from poly(gamma-glutamic acid) (PGA) and benzylamine by direct amidation in dimethyl sulfoxide (DMSO). Benzylamine and PGA were heated in DMSO for 1 to 26 h at temperatures between 110 and 130 degrees C, producing derivatives of various degrees of benzylamidation as a function of the reaction time and temperature. Neither any carboxyl-activating agent nor catalyst is needed for the reaction to proceed. After purification by dialysis, the product was identified by 1H and 13C 1D and 2D NMR in DMSO-d(6). BzPGA prepared by the new direct amidation method was identical to that obtained with a conventional carbodiimide-mediated reaction in water. The one-pot amidation procedure described in the present article can probably be applied to the synthesis of amides from other amines and carboxylic acids.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amides / chemistry
  • Benzylamines / chemistry*
  • Dimethyl Sulfoxide / chemistry
  • Polyglutamic Acid / chemical synthesis
  • Polyglutamic Acid / chemistry*

Substances

  • Amides
  • Benzylamines
  • benzylamidated poly(gamma-glutamic acid)
  • Polyglutamic Acid
  • benzylamine
  • Dimethyl Sulfoxide