## Abstract The different behavior of 2‐(4‐methoxyphenyl)‐ and 2‐(2‐methoxyphenyl)ethylamine and the rearrangement of both products (IV) and (VI) to the novel heterocyclic system (V) are discussed [no yield is given for the rearrangement from (VI) into (V)].
Rearrangement of 2-bromo-N-quinoline-8-yl-acetamide leading to new heterocycle
✍ Scribed by Dipjyoti Kalita; Jubaraj B. Baruah
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2010
- Tongue
- English
- Weight
- 285 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.320
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✦ Synopsis
Abstract
magnified image A four fused rings containing heterocyclic compound is formed in the reaction between 2‐bromo‐N‐quinoline‐8‐yl‐acetamide, 2‐(4‐methoxyphenyl)ethylamine, and acetone in the presence of potassium carbonate; the heterocycle undergoes further reaction with perchloric acid to form a perchlorate salt of a quinoxaline derivative. J. Heterocyclic Chem., (2010).
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