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A novel synthesis of 1-substituted 2H-isoquinolin-3-ones

✍ Scribed by Alicia S. Cánepa; Rodolfo D. Bravo


Publisher
Journal of Heterocyclic Chemistry
Year
2004
Tongue
English
Weight
36 KB
Volume
41
Category
Article
ISSN
0022-152X

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✦ Synopsis


Abstract

The intramolecular cyclization of 2‐acylphenylacetonitriles 1 under strongly acidic conditions easily affords 1‐substituted 2__H__‐isoquinolin‐3‐ones 2 in excellent yields.


📜 SIMILAR VOLUMES


Reaction of 3-substituted and 4-bromo-3-
✍ Cyril Odianose Usifoh 📂 Article 📅 2001 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 39 KB

## Abstract Isoquinolinones were brominated using __N__‐bromosuccinimide in dimethylformamide at room temperature to give 4‐bromo‐3‐substituted isoquinolin‐1‐(2__H__)‐ones. The reaction of these isoquinolinones with propargyl bromide in the presence of anhydrous potassium carbonate yielded __N__ an