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首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Synthesis of Novel Structurally Diverse N-Mono- and N,N-Disubstituted Benzimidazol-2-one Derivatives by the Alkylations of 1,3-Dihydro-2H-benzimidazol-2-one with Some Alkyl Halides under Transfer Catalysis Conditions
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Synthesis of Novel Structurally Diverse N-Mono- and N,N-Disubstituted Benzimidazol-2-one Derivatives by the Alkylations of 1,3-Dihydro-2H-benzimidazol-2-one with Some Alkyl Halides under Transfer Catalysis Conditions

机译:通过1,3-二氢-2H-苯并咪唑-2-烷基化合物的烷基化合成新颖的结构各种N-单 - 和N,N-二取代的苯并咪唑-2-一种衍生物,其在转移催化条件下具有一些烷基卤化物

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摘要

A series of N-mono- and N,N-disubstituted benzimidazol-2-one derivatives optionally substituted on both secondary amine functionalities were prepared with excellent yields by reacting 1,3-dihydro-2H-benzimidazol-2-one in one and two steps respectively with various alkyl halides under phase transfer catalytic conditions. One of the synthesized N,N-disubstituted benzimidazol-2-one derivatives underwent a regiospecific 1,3-dipolar cycloaddition reaction at its side allyl substituent with the in situ generated 4-chloro benzonitrile N-oxide from 4-chlorobenzaldoxime to afford in good yield the corresponding N,N-disubstituted derivative incorporating the 2,5-dihydro-isoxazole nucleus in one of the side chain. All the new compounds were fully characterized by their physical and spectroscopic data.
机译:通过反应1,3-二氢-2H-苯并咪唑-2-1,制备任选地被二次胺官能团取代的一系列n-mono-和n,N-二取代的苯并咪唑-2-一种衍生物,通过使1,3-二氢-2h-苯并咪唑-2-一度反应 分别在相转移催化条件下分别具有各种烷基卤化物的步骤。 其中一种合成的N,N-二取代的苯并咪唑-2-一种衍生物在其侧烯丙基取代基在其原位产生的4-氯苯腈N-氧化物中获得的再生1,3-偶极环加入反应,从4-氯苯甲醛中得到良好 产生相应的N,N-二取代衍生物,其掺入侧链之一中的2,5-二氢异恶唑核。 所有新化合物都是通过其物理和光谱数据的完全表征。

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