Àá½Ã¸¸ ±â´Ù·Á ÁÖ¼¼¿ä. ·ÎµùÁßÀÔ´Ï´Ù.

»õ·Î¿î 4H-1,3,4-Oxadiazino[5,6-b]quinoxaline À¯µµÃ¼µéÀÇ ÇÕ¼º

Synthesis of 4H-1,3,4-Oxadiazino[5,6-b]quinoxaline Derivatives

´ëÇÑÈ­ÇÐȸÁö 1998³â 42±Ç 4È£ p.449 ~ 453
±èµ¿Àº, ±èÈ£½Ä,
¼Ò¼Ó »ó¼¼Á¤º¸
±èµ¿Àº ( Kim Tong-Eun ) - Catholic Universitry of Taegu-Hyosung Department of Chemistry
±èÈ£½Ä ( Kim Ho-Sik ) - Catholic Universitry of Taegu-Hyosung Department of Chemistry

Abstract

6-Chloro-2-hydrazinoquinoxaline 4-oxide(11)¿Í ethyl chloroglyoxylate¸¦ ¹ÝÀÀ½ÃÄÑ ºÐÀÚ³» °í¸®È­¹ÝÀÀ¿¡ ÀÇÇÑ ethyl 8-chloro-4H-1,3,4-oxadiazino[5,6-b]quinoxaline-2-carboxylate(12)¸¦ ÇÕ¼ºÇÏ¿´´Ù. È­ÇÕ¹° 12¸¦ hydrazine hydrate¿Í ¹ÝÀÀ½ÃÄÑ C2-hydrazinocarbonyl À¯µµÃ¼ 13ÀÌ ÇÕ¼ºµÇ¾ú´Âµ¥, À̰ÍÀ» ġȯ º¥Áî¾Ëµ¥È÷µå·ù ¹× ÇìÅ׷ξƸ± ¾Ëµ¥È÷µå·ù¿Í ¹ÝÀÀ½ÃÄÑ 8-chloro-2-(substituted benzylidenehydrazinocarbonyl)-4H-1,3,4-oxadiazino[5,6-b]quinoxaline·ù(14) ¹× 8-chloro-2-[(2-substituted methylidene)hydrazinocarbonyl]-4H-1,3,4-oxadiazino[5,6-b]quinoxalinefb(15)¸¦ °¢°¢ ÇÕ¼ºÇÏ¿´´Ù.

The reaction of 6-chloro-2-hydrazinoquinoxaline 4-oxide (11) with ethyl chloroglyoxylate provided ethyl 8-chloro-4H-1,3,4-oxadiazino[5,6-b]quinoxaline-2-carboxylate (12) through the intramolecular cyclization. The reaction of 12 with hydrazine hydrate afforded the C2-hydrazinocarbonyl derivative 13, whose reactions with substituted benzaldehydes or heteroaryl aldehydes provided 8-chloro-2-(substituted benzylidenehydrazinocarbonyl)-4H-1,3,4-oxadiazino[5,6-b]quinoxalines (14) or 8-chloro-2-[(2-substituted methylidene)hydrazinocarbonyl]-4H-1,3,4-oxadiazino[5,6-b]quinoxalines(15), respectively.

Ű¿öµå

¿ø¹® ¹× ¸µÅ©¾Æ¿ô Á¤º¸

µîÀçÀú³Î Á¤º¸