Convenient synthesis of 6-substituted-2-chloro-5,12-dihydro-5-oxobenzoxazolo[3,2-a]quinolines and N-acylated-3-chlorodibenz[b,e][1,4]oxazepin-11(5H)-ones

Convenient synthesis of variously substituted 2‐chloro‐5,12‐dihydro‐5‐oxobenzoxazolo[3,2‐a]quinolines at the 6‐position and N‐acylated‐3‐chlorodibenz[b,e][1,4]oxazepin‐11(5H)‐ones are reported. The former compounds were obtained in 65–93% yield by simply heating N‐acyl‐4‐chloro‐N‐(2‐hydroxyphenyl)‐a...

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Veröffentlicht in:Journal of heterocyclic chemistry 1997-03, Vol.34 (2), p.485-488
Hauptverfasser: Chung, Sang J., Joo, Keum Chan, Kim, Dong H.
Format: Artikel
Sprache:eng
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Zusammenfassung:Convenient synthesis of variously substituted 2‐chloro‐5,12‐dihydro‐5‐oxobenzoxazolo[3,2‐a]quinolines at the 6‐position and N‐acylated‐3‐chlorodibenz[b,e][1,4]oxazepin‐11(5H)‐ones are reported. The former compounds were obtained in 65–93% yield by simply heating N‐acyl‐4‐chloro‐N‐(2‐hydroxyphenyl)‐anthranilic acids in acetic anhydride for 4 hours, and the latter by heating sodium salt of N‐acyl‐4‐chloro‐N‐(2‐hydroxyphenyl)anthranilic acids with acetic anhydride.
ISSN:0022-152X
1943-5193
DOI:10.1002/jhet.5570340221