首页> 外文期刊>Research Journal of Pharmaceutical Sciences >PC-Model Studies of 7 methoxy- 2H-3-Aryl-3,4-dihydro-1,3 benzoxazine-Aryl-3, 4-dihydro-4-methyl 7 methoxy -1, 3 benzoxazine Biological activity
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PC-Model Studies of 7 methoxy- 2H-3-Aryl-3,4-dihydro-1,3 benzoxazine-Aryl-3, 4-dihydro-4-methyl 7 methoxy -1, 3 benzoxazine Biological activity

机译:7-甲氧基-2H-3-芳基-3,4-二氢-1,3苯并恶嗪的PC模型研究-芳基-3,4-二氢-4-甲基7甲氧基-1,3苯并恶嗪的生物活性

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An optimization of the reaction conditions in solvent free and solution phase microwave assisted synthesis of (7 Methoxy) 2H-3-Aryl-3, 4-dihydro-1,3 benzoxazine derivatives.The reported methods for the synthesis of substituted benzoxazine derivatives. 2-Hydroxy3-methoxy benzaldehyde and 1-(2-Hydroxyphenyl) ethanol on the reaction with different primary aromatic amines gave methoxy 2-(arylimino) methylphenols and 2-[1-arylimino) ethyl] phenols respectively Synthesized Compound (1). on reduction with sodium borohydride gave 2- methoxy (arylamino) methylphenols and 2- [1-(aryl amino) ethyl] phenols, Synthesized Compound (2). Which further cyclised with formaldehyde to form the final synthetic derivatives as methoxy 2H-3-aryl-3, 4-dihydro-1, 3-benzoxazines and 2H-3-aryl-3, 4-dihydro-4 methyl- 1,3-methoxy benzoxazines. PC-model values, antimicrobial and antifungal activity studies.
机译:在无溶剂和溶液相微波辅助条件下优化反应条件有助于合成(7 Methoxy)2H-3-Aryl-3,4-dihydro-1,3苯并恶嗪衍生物。报道了取代苯并恶嗪衍生物的合成方法。 2-羟基3-甲氧基苯甲醛和1-(2-羟基苯基)乙醇与不同的伯芳族胺反应,分别得到甲氧基2-(芳基)甲基酚和2- [1-芳基)乙基]酚,分别合成了化合物(1)。用硼氢化钠还原后,得到2-甲氧基(芳基氨基)甲基酚和2- [1-(芳基氨基)乙基]酚,合成了化合物(2)。其进一步与甲醛环化以形成最终的合成衍生物,如甲氧基2H-3-芳基-3,4-二氢-1,3-苯并恶嗪和2H-3-芳基-3,4-二氢-4甲基-1,3-甲氧基苯并恶嗪。 PC模型值,抗微生物和抗真菌活性研究。

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