Potikha, L. M. published the artcileCondensed isoquinolines. Part 21. Condensation of o-bromomethylphenylacetonitrile with substituted anthranilic acids, Recommanded Product: 2-(2-(Bromomethyl)phenyl)acetonitrile, the main research area is bromomethylbenzeneacetonitrile anthranilate cyclocondensation; isoquinoquinazolinone hydro preparation tautomerism.
The reaction of substituted anthranilic acids and esters with ortho-bromomethylphenylacetonitrile gives 2,3-disubstituted 7,12-dihydro-5H-isoquino[2,3-a]quinazolin-5-one hydrobromides. It was found that 7,12-dihydro-5H-isoquino[2,3-a]quinazolin-5-ones can exist in the two tautomeric imine and enamine forms. The tautomeric equilibrium position depends on the nature and position of the substituent in the quinazoline fragment. The borohydride reduction, oxidation, and reaction of the 7,12-dihydro-5H-isoquino[2,3-a]quinazolin-5-ones with electrophilic reagents was studied.
Chemistry of Heterocyclic Compounds (New York, NY, United States) published new progress about Aromatic amino acids Role: RCT (Reactant), RACT (Reactant or Reagent). 73217-11-5 belongs to class nitriles-buliding-blocks, name is 2-(2-(Bromomethyl)phenyl)acetonitrile, and the molecular formula is C9H8BrN, Recommanded Product: 2-(2-(Bromomethyl)phenyl)acetonitrile.
Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts