Unsaturated cyclic ureas as new nontoxic biodegradable transdermal penetration enhancers I: Synthesis

J Pharm Sci. 1988 Nov;77(11):967-71. doi: 10.1002/jps.2600771115.

Abstract

A new concept was implemented to reduce the toxicity of some new biodegradable transdermal penetration enhancers. These enhancers consist of 1-alkyl-4-imidazolin-2-one and a long-chain alkyl ester group at the N-3 position. The synthesis involves N-alkylation of the parent compound with soft alkylating agents which were prepared in high yields by an improved method. A phase transfer catalysis technique using KOH as the base, tetrabutylammonium bromide as the catalyst, and toluene as the solvent was found to be most effective in the N-alkylation step.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adjuvants, Pharmaceutic / chemical synthesis*
  • Administration, Cutaneous
  • Alkylating Agents / pharmacology
  • Chemical Phenomena
  • Chemistry
  • Skin Absorption / drug effects*
  • Urea

Substances

  • Adjuvants, Pharmaceutic
  • Alkylating Agents
  • Urea