New synthesis and reactivity of 3-bromoacetyl-4-hydroxy-6-methyl-2H-pyran-2-one with binucleophilic amines
作者:Djamila Hikem-Oukacha、Maamar Hamdi、Artur M. S. Silva、Rachedi Yahia
DOI:10.1002/jhet.507
日期:2011.1
nyl)vinyl]‐6‐methyl‐2H‐pyran‐2‐one, 1‐(2,4‐dinitrophenyl)‐7‐methyl‐2,3‐dihydro‐1H‐pyrano[4,3‐c]pyridazine‐4,5‐dione, 3‐(3,4‐dihydroquinoxalin‐2‐yl)‐4‐hydroxy‐6‐methyl‐2H‐pyran‐2‐one/3‐(3,4‐dihydroquinoxalin‐2‐yl)‐6‐methyl‐2H‐pyran‐2,4(3H)‐dione, 6‐methyl‐3‐(3,4‐dihydroquinoxalin‐2‐yl)‐2H‐pyran‐2,4(3H)‐dione, and (E)‐3‐(2H‐benzo[b][1,4]thiazin‐3(4H)‐ylidene)‐6‐methyl‐2H‐pyran‐2,4(3H)‐dione were fully
3-(溴乙酰基)-4-羟基-6-甲基-2 H-吡喃-2-酮是通过脱氢乙酸(DHAA)与溴在冰醋酸中的反应合成的。溴化DHAA与链烷二胺,苯肼,邻苯二胺和邻氨基苯硫醇的反应合成了新型杂环产物。获得的新产品3-(2 - N-取代乙酰基)-4-羟基-6-甲基-2- H-吡喃-2-酮,4-羟基-3- [1-羟基-2-(2-苯基肼基) []乙烯基] -6-甲基-2 H-吡喃-2--1,1- (2,4-二硝基苯基)-7-甲基-2,3-二氢-1H-吡喃[4,3- c ]哒嗪- 4,5-二酮,3-(3,4-二氢喹喔啉-2-基)-4-羟基-6-甲基-2 H吡喃-2-一/ 3-(3,4-二氢喹喔啉-2-基)-6-甲基-2 H-吡喃-2,4(3 H)-二酮,6-甲基-3-(3,4 -二氢喹喔啉-2-基)-2 H-吡喃-2,4(3 H)-二酮和(E)-3-(2 H-苯并[b] [1,4]噻嗪-3(4 H) -亚丙基)-6-甲基-2