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Synthesis of some [1,2,4]triazino[5,6‐ b ]quinoline derivatives
Author(s) -
Stýskala Jakub,
Slouka Jan,
Lycka Antonín
Publication year - 2002
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.5570390630
Subject(s) - chemistry , quinoline , carbamate , alkaline hydrolysis , hydrolysis , aryl , medicinal chemistry , ethyl carbamate , organic chemistry , alkyl , food science , wine
By coupling of diazonium salts with ethyl N ‐(4‐oxo‐1,4‐dihydroquinolin‐2‐yl)carbamate 4 , the corresponding 3‐arylazocompounds 5 were obtained. These ones were cyclized thermally or in alkaline medium to the corresponding 2‐aryl‐2,3,5,10‐tetrahydro‐[1,2,4]triazino[5,6‐ b ]quinolin‐3,10‐diones 6 . Compounds 6 were transformed by alkaline hydrolytic splitting to the corresponding 2‐amino‐3‐arylazo‐1,4‐dihydroquino‐lin‐4‐ones 7. Starting carbamate 4 was prepared by a two‐step synthesis from 2‐amino‐1,4‐dihydroquinolin‐4‐one 1.
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