Rearrangement  of 2‐bromo‐ N ‐quinoline‐8‐yl‐acetamide leading to new heterocycle | Zendy

Kalita Dipjyoti | Zendy; Baruah Jubaraj B. | Zendy

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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).

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