SHORT COMMUNICATIONS
Optimization of Conditions for the Synthesis and Oxidation of 5,8-Dimethoxy-2-methyl-3,4-dihydroisoquinolin-1(2H)-one into Novel 2-Methylisoquinoline-1,5,8(2H)-trione
Published
May 2, 2020
Keywords
- catalyst ratio,
- ceric ammonium nitrate,
- isoquinolones,
- N-methylation,
- oxidation
How to Cite
(1)
Ali, B.; Ahmed, F.; Shafiq, N.; Nasrula, M. Optimization of Conditions for the Synthesis and Oxidation of 5,8-Dimethoxy-2-Methyl-3,4-Dihydroisoquinolin-1(2H)-One into Novel 2-Methylisoquinoline-1,5,8(2H)-Trione. Orbital: Electron. J. Chem. 2020, 12, 30-33.
Copyright (c) 2020 Orbital: The Electronic Journal of Chemistry
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Abstract
Due to stability issue of isoquinolone’s their N-methylation is a challenging task, achieved the synthesis of N-methylated 2-methylisoquinoline-1,5,8(2H)-trione using readily available precursor 2-(2,5-dimethoxyphenyl)ethanamine via multistep strategy, finally oxidation of 5,8-dimethoxy-2-methyl-3,4-dihydroisoquinolin-1(2H)-one with ceric ammonium nitrate (CAN) lead to target isoquinolone in good yield, further oxidation conditions in final step were optimized using different catalyst ratio, reaction time and temperature conditions.