Author:
Fuentes José J.,Lenoir Jacques A.
Abstract
Spectroscopic results from mono- and dibenzylidene derivatives of 1-alkylguanazoles establish that alkylation of 3,5-diamino-1,2,4-triazole (guanazole) with alkyl halides in basic non-aqueous media occurs at position N-1.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
15 articles.
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1. Synthon-Based Approach to the Design of Macroheterocyclic Compounds Using Diaminothiadiazoles and Diamonotriazoles;Russian Journal of General Chemistry;2018-09
2. Reactivity of 2-amino[1,2,4]triazolo[1,5-а]-pyrimidines with various saturation of the pyrimidine ring towards electrophiles;Chemistry of Heterocyclic Compounds;2015-11
3. Mesomorphic Properties and Computer Simulation of Guanazole Derivatives and Their Mixtures;Acta Physica Polonica A;2015-04
4. 2,1-Benzothiazine 2,2-dioxides 10*. Reaction of alkyl 1-R-4-hydroxy-2,2-dioxo-1Н-2λ6,1-benzothiazine-3-carboxylates with 1H-1,2,4-triazol-5-amine;Chemistry of Heterocyclic Compounds;2015-01
5. Reactivity of C-Amino-1,2,4-triazoles toward Electrophiles: A Combined Computational and Experimental Study of Alkylation by Halogen Alkanes;The Journal of Organic Chemistry;2014-12-15