One-Pot Three-Component Reaction for the Synthesis of 3,4-Dihydroquinazolines and Quinazolin-4(3 H )-ones.
Shiwei ChenYeong Shin JiYuri ChoiSo Won YounPublished in: The Journal of organic chemistry (2024)
A highly efficient and straightforward one-pot synthesis of diversely substituted 3,4-dihydroquinazolines and quinazolin-4(3 H )-ones has been achieved through a domino three-component assembly reaction of arenediazonium salts, nitriles, and bifunctional aniline derivatives. This new protocol involves three C-N bond formations through the initial formation of N -arylnitrilium intermediates from arenediazonium salts and nitriles, followed by the sequential nucleophilic addition and cyclization reactions with bifunctional anilines, leading to such N -heterocyclic compounds of biological and pharmacological importance. This method offers a simple, expedient, and robust approach with the use of amenable and easily accessible reactants/reagents under metal-free mild conditions, good functional group tolerance, and high efficiency. The synthetic applications were also demonstrated by derivatization of the products obtained from these processes and syntheses of a diverse range of valuable polycyclic N -heterocycles.
Keyphrases
- highly efficient
- high efficiency
- ionic liquid
- randomized controlled trial
- ms ms
- molecular docking
- electron transfer
- gas chromatography mass spectrometry
- high performance liquid chromatography
- liquid chromatography tandem mass spectrometry
- simultaneous determination
- liquid chromatography
- solid phase extraction
- tandem mass spectrometry
- mass spectrometry
- gas chromatography
- molecular dynamics simulations