Intramolecular cyclization reactions of arylpropargyl amides of electron-deficient α,β-alkenyl carboxylates and related compounds

Intramolecular cyclization reactions of arylpropargyl amides of electron-deficient alpha,beta-alkenyl carboxylates such as fumarates and ethenetricarboxylates were investigated. The reaction of the fumaramides with a base, Et3N or DBU in xylenes at 140 degrees C under air gave benz[f]isoindoline derivatives in 21-63% yields. The benz[f]isoindolines may be produced via the formation of an allenic intermediate, intramolecular Diels-Alder reaction, proton transfer, and dehydrogenation by oxygen. The suitable bases and the product yields depend on the substituents on the benzene ring. On the other hand, the reaction of the amides of fumarate and ethenetricarboxylate by heating in DMSO gave aroyl-substituted pyrrolidine derivatives as major products, probably via addition of water under metal-free conditions. Furthermore, cyclization reactions of H and Me substituted alkyne derivatives were investigated for comparison. The selective formation of various types of products, such as ethyl 2-(1-benzyl-4-formyl-2-oxopyrrolidin-3-yl)acetate and diethyl 2-(1-benzyl-2-oxo-4-vinylidenepyrrolidin-3-yl)malonate, was found, depending upon the alkyne substituents and the reaction conditions. The reaction mechanisms have been discussed using density functional theory (DFT) calculations.

Automated summary

This study investigated intramolecular cyclization reactions of arylpropargyl amides of electron-deficient alpha, beta-alkenyl carboxylates, such as fumarates and ethenetricarboxylates. The reactions yielded benz[f]isoindoline derivatives when fumaramides were reacted with a base, Et3N or DBU, in xylenes under air. Aroyl-substituted pyrrolidine derivatives were obtained as major products when amides of fumarate and ethenetricarboxylate were heated in DMSO. The reaction mechanisms were discussed using density functional theory (DFT) calculations.