Literature DB >> 25030664

A concise synthesis of benzimidazoles via the microwave-assisted one-pot batch reaction of amino acids up to a 10-g scale.

Pai Peng1, Jin-Feng Xiong, Guang-Zhen Mo, Jia-Li Zheng, Ren-Hong Chen, Xiao-Yun Chen, Zhao-Yang Wang.   

Abstract

An efficient method for the synthesis of aminomethyl benzimidazoles is developed by using a one-pot batch reaction between amino acids and o-phenylenediamines. This reaction proceeds smoothly in an unmodified household microwave oven, even though scale-up is to 10 g. A desirable method for the quick synthesis of benzimidazoles, which are used as a kind of important intermediates in drug synthesis, is provided by the scale-up utilization of amino acid resource.

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Year:  2014        PMID: 25030664     DOI: 10.1007/s00726-014-1794-z

Source DB:  PubMed          Journal:  Amino Acids        ISSN: 0939-4451            Impact factor:   3.520


  2 in total

1.  Furanonyl amino acid derivatives as hemostatic drugs: design, synthesis and hemostasis performance.

Authors:  Neng Wang; Jian-Yun Lin; Shi-He Luo; Yong-Jun Zhou; Kai Yang; Ren-Hong Chen; Guo-Xian Yang; Zhao-Yang Wang
Journal:  Amino Acids       Date:  2022-03-19       Impact factor: 3.520

2.  Crystal structure and Hirshfeld surface analysis and of 2-ammoniumylmeth-yl-1H-benzimidazol-3-ium chloride monohydrate.

Authors:  Pinar Sen; Sevgi Kansiz; Necmi Dege; S Zeki Yildiz; Galyna G Tsapyuk
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2018-09-28
  2 in total

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