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首页> 外文期刊>Tetrahedron >Base promoted facile route to functionalized benzo[b][1,8] naphthyridin-2-(1H)-ones from N-benzyl-N-(3-cyanoquinolin-2-yl) acetamides
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Base promoted facile route to functionalized benzo[b][1,8] naphthyridin-2-(1H)-ones from N-benzyl-N-(3-cyanoquinolin-2-yl) acetamides

机译:碱促进了从N-苄基-N-(3-氰基喹啉-2-基)乙酰胺中官能化的苯并[b] [1,8]萘啶-2-(1H)-的轻松合成路线

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摘要

A facile synthesis of 4-amino-N-benzylbenzo[b][1,8]naphthyridin-2(1H)-ones 3 is described from Nbenzyl- N-(3-cyanoquinolin-2-yl)acetamides 2 with t-BuOK in excellent yields in mild conditions. These reactions proceeded at room temperature under aerobic atmosphere in very short period. The cyclization reactions were also extended with N-alkyl amino acetamide analogues affording the products in good yields.
机译:从N-苄基-N-(3-氰基喹啉-2-基)乙酰胺2用t-BuOK轻松合成4-氨基-N-苄基苯并[b] [1,8]萘啶-2(1H)-ones 3在温和条件下的产量极高。这些反应在室温下在有氧气氛下进行的时间很短。还用N-烷基氨基乙酰胺类似物扩展了环化反应,从而以高收率提供了产物。

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