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Rearrangement of 2‐bromo‐ N ‐quinoline‐8‐yl‐acetamide leading to new heterocycle
Author(s) -
Kalita Dipjyoti,
Baruah Jubaraj B.
Publication year - 2010
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.320
Subject(s) - chemistry , acetamide , quinoline , potassium carbonate , quinoxaline , perchloric acid , perchlorate , salt (chemistry) , medicinal chemistry , derivative (finance) , acetone , potassium perchlorate , organic chemistry , ion , financial economics , economics
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).