Open AccessEthyl 5‐chloro‐9‐ethoxy‐2‐oxo‐2 H ‐pyrano[2,3‐ g ]quinoline‐8‐carboxylate
Author(s) -
Oliveira César D. de,
Romeiro Gilberto A.,
Skakle Janet M. S.,
Wardell James L.,
Wardell Solange M. S. V.
Publication year - 2006
Publication title -
acta crystallographica section e
Language(s) - English
Resource type - Journals
ISSN - 1600-5368
DOI - 10.1107/s160053680600715x
Subject(s) - isostructural , quinoline , chemistry , ring (chemistry) , alkoxy group , carboxylate , molecule , hydrogen bond , medicinal chemistry , stereochemistry , alkylation , crystal structure , crystallography , organic chemistry , catalysis , alkyl
The title compound, C 17 H 14 ClNO 5 has been shown to be isostructural with the bromo analogue, confirming the site of alkylation within the structure and the pyranoquinoline ring system. As with the bromo analogue, the molecules are linked by a C—H⋯O hydrogen bond forming C (5) chains along [001].