Photooxidation of 2,3-dihydroquinazolin-4(1H)-ones: retention or elimination of 2-substitution

A series of mono and disubstituted 2,3-dihydroquinazolin-4(1H)-ones (DHQZs) were synthesized and the electronic and steric effects of the C-2- and N-3-substitutions on the retention or elimination of the C-2-substitution by exposing them to the ultraviolet light were investigated. Electron transfer from photo-excited dihydroquinazolinones to chloroform solvent is proposed, in which both lone pairs on the N-1- and N-3-atoms can be involved in this process. The extent of the N-1- and N-3-atoms contributions in this electron-transfer process and also the retention or elimination of the C-2-substitutions are dependent on the nature and steric hindrance of both C-2- and N-3-substitutions. The experimental results are supported by the computational studies. Graphic abstract [GRAPHICS] Photoinduced electron-transfer reaction of a series of mono and disubstituted 2,3- dihydroquinazolin-4(1H)-ones was investigated.

Automated summary

The photoinduced electron-transfer reaction of a series of mono and disubstituted 2,3-dihydroquinazolin-4(1H)-ones was studied, with the contribution of N-1 and N-3 atoms affecting the retention or elimination of C-2 substitutions depending on the nature and steric hindrance of the substitutions.