## Abstract A reaction mechanism with in situ generated HCl as primary promoter is proposed.
Efficient 2,4,6-trichloro-1,3,5-triazine-catalyzed synthesis of 2-arylbenzothiazoles and bisbenzothiazoles by condensation of 2-aminithiophenol with aldehydes under mild conditions
โ Scribed by Behrooz Maleki; Davood Azarifar; Seyede Fateme Hojati; Hojat Veisi; Mostafa Gholizadeh; Hafezeh Salehabadi; Mona Khodaverdian Moghadam
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2010
- Tongue
- English
- Weight
- 254 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.462
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โฆ Synopsis
Abstract
2,4,6โTrichloroโ1,3,5โtriazine efficiently catalyzed the condensation reactions between 2โaminothiophenol and aromatic aldehydes to afford 2โarylbenzothiazolles in goodโtoโexcellent yields. Simple and mild reaction conditions, the use of a cheap catalyst and easy work up, and isolation are notable features of this method. J. Heterocyclic Chem., (2011).
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