synthesis and characterization of 2-methoxy-6-phenyl-5h-pyrrolo[3,4-b]pyrazine-5,7(6h)-dione and 7-hydroxy-3-methoxy-6-phenyl-6,7-dihydro-5h-pyrrolo[3,4-b]pyrazine-5-one and some derivatives

K. Saraswat, Shashi Pandey
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Abstract

The process of producing a series of chemical combinations of 2-methoxy-6-phenyl-5H-pyrrolo[3,4-b]pyrazine-5,7(6H)-dione descendant [103-110] and 7-hydroxy-3-methoxy-6-phenyl-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazine-5-one descendant [111-119], magnetized significant regard in prospective of curative requisition. The fusion was conved by conducting 2-hydroxyfuro [3,4-b]pyrazine-5,7-dione with equimolar Bromomethane in dry toluene at 0-5C to get combination 2-methoxyfuro[3,4- b ]pyrazine-5,7-dione which further at reflux condense with aniline derivatives to 2-methoxy-6-phenyl-5H-pyrrolo[3,4-b]pyrazine-5,7(6H)-dione derivatives with Potassium borohydride granules in methanol at 0-20C converted to 7-hydroxy-3-methoxy-6-phenyl-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazine-5-one descendant. The distinctive nature of all the incorporated combinations have been described by manipulating basic inspection (elemental analysis), IR, 1 H NMR, 13 C NMR spectroscopical.
2-甲氧基-6-苯基-5h-吡咯[3,4-b]吡嗪-5,7(6h)-二酮和7-羟基-3-甲氧基-6-苯基-6,7-二氢-5h-吡咯[3,4-b]吡嗪-5-酮及其衍生物的合成与表征
2-甲氧基-6-苯基- 5h -吡咯啉[3,4-b]吡嗪-5,7(6H)-二酮后代[103-110]和7-羟基-3-甲氧基-6-苯基-6,7-二氢- 5h -吡咯啉[3,4-b]吡嗪-5-一后代[111-119]的一系列化学组合的过程在治疗需求的前景中引起了重要的关注。将2-羟基呋喃[3,4-b]吡嗪-5,7-二酮与等摩尔溴甲烷在0-5C的干燥甲苯中进行熔合,得到2-甲氧基呋喃[3,4-b]吡嗪-5,7-二酮的组合,再与苯胺衍生物回流缩合得到2-甲氧基-6-苯基- 5h -吡罗[3,4-b]吡嗪-5,7(6H)-二酮衍生物与硼氢化钾颗粒在0-20C的甲醇中转化为7-羟基-3-甲氧基-6-苯基-6,7-二氢- 5h -吡罗[3,4-b]吡嗪-5- 1后代。通过操作基本检查(元素分析),IR, 1h NMR, 13c NMR光谱描述了所有合并组合的独特性质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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