Literature DB >> 28494581

Synthesis of 5-Amino and 3,5-Diamino Substituted 1,2,4-Thiadiazoles by I2-Mediated Oxidative N-S Bond Formation.

Bingnan Wang1, Yinggao Meng1, Yiming Zhou1, Linning Ren1, Jie Wu1, Wenquan Yu1, Junbiao Chang1.   

Abstract

An oxidative N-S bond formation reaction has been established for 1,2,4-thiadiazole synthesis employing molecular iodine as the sole oxidant. The features of the present reaction include no use of transition metals, mild reaction conditions, simple operation, and short reaction time. This versatile synthetic approach is broadly applicable to a variety of imidoyl and guanyl thiourea substrates to produce 5-amino and 3,5-diamino substituted 1,2,4-thiadiazole derivatives, respectively, in an efficient and scalable fashion.

Entities:  

Year:  2017        PMID: 28494581     DOI: 10.1021/acs.joc.7b00814

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  External oxidant-free and transition metal-free synthesis of 5-amino-1,2,4-thiadiazoles as promising antibacterials against ESKAPE pathogen strains.

Authors:  Anton Shetnev; Marina Tarasenko; Valentina Kotlyarova; Sergey Baykov; Kirill Geyl; Svetlana Kasatkina; Nikolina Sibinčić; Vladimir Sharoyko; Elizaveta V Rogacheva; Liudmila A Kraeva
Journal:  Mol Divers       Date:  2022-05-31       Impact factor: 2.943

2.  Synthesis of novel series of 3,5-disubstituted imidazo[1,2-d] [1,2,4]thiadiazoles involving SNAr and Suzuki-Miyaura cross-coupling reactions.

Authors:  Clémentine Pescheteau; Matthieu Place; Alexandru Sava; Lea Nunes; Lenuta Profire; Sylvain Routier; Frédéric Buron
Journal:  RSC Adv       Date:  2022-02-23       Impact factor: 3.361

  2 in total

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