پديدآورندگان :
Tirgir Farhang Tirgir_58@yahoo.com Islamic Azad university, shahrehord branch , Ghafouri hafshejani Masoumeh Islamic Azad university, shahrehord branch , Amiri Nasrin Islamic Azad university, shahrehord branch
چكيده فارسي :
The One-Pot multicomponent reaction (MCR) was an attractive broad area ofresearch
in the synthesis of N-containing heterocyclic scaffolds such as the 3,4-dihydropyridin-2-
1H-(thiones) (DHPMs) and theirheterocyclic derivatives [1–3].Organocatalysts possess
advantages such as cost-effectiveness, ready availability, a metal-freeenvironment,
relatively low toxicity, simple functionality, non-sensitivity to airand moisture, promotion
of a variety of chemical transformations via variousactivation modes, mildness of the
reaction conditions required, huge potential forthe development of large-scale production
of Biginelli reaction [3].In this work, N,N-Diphthalimide (DPHI) was directly synthesized
via reaction of phthalicdianhidride with thiouera in solvent free. This reagent is found to
be an efficient solid acidic organic catalyst in the Biginelli reaction. The three-component
reaction of aryl aldehydes derivedthiourea, and ethyl acetoacetate or acetylacetone occurs
by means of 10 mol % of (DPHI) insolvent-free reaction conditions. The present
methodology is a green approach to access a series of 3,4-dihydropyrimidin-2(1H)-
thiones in high yields. In addition, the use of DPHI as the catalyst offers several notable
features such as simple operational procedure, no use of hazardous organic solvents, and
recyclability of catalyst. (Figure 1).