Bhat, Mashooq A. published the artcileBiginelli synthesis of novel dihydropyrimidinone derivatives containing phthalimide moiety, Application In Synthesis of 86-51-1, the main research area is isoindolylphenylcarbonyl dihydropyrimididnone preparation; dimethylaminopropenoylphenyl isoindole urea benzaldehyde Beginelli reaction.
Novel Biginelli compounds, 5-benzoyl-substituted phenyl-3,4-dihydropyrimidin-2(1H)-one-1H-isoindole-1,3(2H)- dione were synthesized from enaminone, 2-{4-[(2E)-3-(dimethylamino)prop-2-enoyl]phenyl}-1H-isoindole-1,3(2H)- dione, which was synthesized by refluxing 2-(4-acetylphenyl)-1H-isoindole-1,3(2H)-dione, with dimethylformamidedimethylacetal (DMF-DMA) without solvent for 12 h. The compound 2-(4-acetylphenyl)-1H-isoindole-1,3(2H)-dione was obtained by reacting phthalic anhydride with para-aminoacetophenone in glacial acetic acid for 2 h. This method was employed to synthesize the dihydropyrimidinone derivatives containing phthalimide moiety. Structures of all the synthesized compounds were characterized by spectroscopic methods.
Journal of Chemistry published new progress about Aryl ketones Role: RCT (Reactant), RACT (Reactant or Reagent). 86-51-1 belongs to class isoquinoline, name is 2,3-Dimethoxybenzaldehyde, and the molecular formula is C9H10O3, Application In Synthesis of 86-51-1.
Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem