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Efficient Copper‐Promoted Tandem Multi‐Component Strategy: The Synthesis of 1‐ Aryl/Alkyl‐5‐( N ‐Benzoylamino) Tetrazoles and Guanidine's
Author(s) -
vali Shaik Baji,
Seelam Mohan,
Tamminana Ramana,
Kammela Prasad Rao
Publication year - 2017
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.201702568
Subject(s) - thiourea , guanidine , chemistry , alkyl , aryl , tandem , combinatorial chemistry , component (thermodynamics) , chloride , benzoyl chloride , copper , medicinal chemistry , organic chemistry , materials science , physics , composite material , thermodynamics
Efficient, simple and multi component methodology has been demonstrated for the construction of l‐Aryl/Alkyl‐5‐( N ‐Benzoylamino) tetrazoles and guanidine's. These compounds can be used as intermediates for the synthesis of heterocyclic compounds such as substituted 2‐( N‐ benzoyl) benzimidazoles and fused cyclic tetrazoles. Target products were obtained from benzyol chloride via in situ consecutive formation of benzoyl isothiocyanates and benzyol aryl thiourea. Moreover, desulphurization was also observed during this methodology. In addition, functional group tolerance and reaction mechanism have also been studied.