Home / Publications / PASE synthesis of 1-azolyl-1H-1,2,4-triazoles by the reaction of diazoazoles with ethyl isocyanoacetate

PASE synthesis of 1-azolyl-1H-1,2,4-triazoles by the reaction of diazoazoles with ethyl isocyanoacetate

6
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Sadchikova E. V., Alexeeva D. L., Nenajdenko V. G. PASE synthesis of 1-azolyl-1H-1,2,4-triazoles by the reaction of diazoazoles with ethyl isocyanoacetate // Mendeleev Communications. 2019. Vol. 29. No. 6. pp. 653-654.
GOST all authors (up to 50) Copy
Sadchikova E. V., Alexeeva D. L., Nenajdenko V. G. PASE synthesis of 1-azolyl-1H-1,2,4-triazoles by the reaction of diazoazoles with ethyl isocyanoacetate // Mendeleev Communications. 2019. Vol. 29. No. 6. pp. 653-654.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.mencom.2019.11.016
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.11.016
TI - PASE synthesis of 1-azolyl-1H-1,2,4-triazoles by the reaction of diazoazoles with ethyl isocyanoacetate
T2 - Mendeleev Communications
AU - Sadchikova, Elena Vladimirovna
AU - Alexeeva, Daria Leonidovna
AU - Nenajdenko, Valentin Georgievich
PY - 2019
DA - 2019/11/01
PB - Mendeleev Communications
SP - 653-654
IS - 6
VL - 29
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{2019_Sadchikova,
author = {Elena Vladimirovna Sadchikova and Daria Leonidovna Alexeeva and Valentin Georgievich Nenajdenko},
title = {PASE synthesis of 1-azolyl-1H-1,2,4-triazoles by the reaction of diazoazoles with ethyl isocyanoacetate},
journal = {Mendeleev Communications},
year = {2019},
volume = {29},
publisher = {Mendeleev Communications},
month = {Nov},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.11.016},
number = {6},
pages = {653--654},
doi = {10.1016/j.mencom.2019.11.016}
}
MLA
Cite this
MLA Copy
Sadchikova, Elena Vladimirovna, et al. “PASE synthesis of 1-azolyl-1H-1,2,4-triazoles by the reaction of diazoazoles with ethyl isocyanoacetate.” Mendeleev Communications, vol. 29, no. 6, Nov. 2019, pp. 653-654. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.11.016.

Abstract

PASE (pot, atom and step economic) synthesis of 1-azolyl-1H-1,2,4-triazole derivatives in up to 91% yield has been accomplished by addition of 5-diazoazoles to ethyl isocyanoacetate.

References

1.
Review: biologically active pyrazole derivatives
Ansari A., Ali A., Asif M., Shamsuzzaman S.
New Journal of Chemistry, 2017
2.
10.1016/j.mencom.2019.11.016_bib0010
Luca
Curr. Med. Chem., 2006
3.
1,2,4-Triazoles: Synthetic approaches and pharmacological importance. (Review)
Al-Masoudi I.A., Al-Soud Y.A., Al-Salihi N.J., Al-Masoudi N.A.
Chemistry of Heterocyclic Compounds, 2006
4.
Synthesis and Biological Applications of Triazole Derivatives – A Review
Sathish Kumar S., P. Kavitha H.
Mini-Reviews in Organic Chemistry, 2013
5.
1,2,4-Triazoles: A Review of Synthetic Approaches and the Biological Activity
Maddila S., Pagadala R., Jonnalagadda S.
Letters in Organic Chemistry, 2013
6.
Synthesis and Evaluation of Anti-inflammatory and Analgesic Activities of New 1,2,4-triazole Derivatives
Ahmadi F., Ghayahbashi M., Sharifzadeh M., Alipoiur E., Ostad S., Vosooghi M., khademi H., Amini M.
Medicinal Chemistry, 2014
7.
Recent advances bioactive 1,2,4-triazole-3-thiones
Küçükgüzel Ş.G., Çıkla-Süzgün P.
European Journal of Medicinal Chemistry, 2015
8.
Advances in synthetic approach to and antifungal activity of triazoles
Shalini K., Kumar N., Drabu S., Sharma P.K.
Beilstein Journal of Organic Chemistry, 2011
9.
10.1016/j.mencom.2019.11.016_bib0045
Bulut
Bull. Chem. Soc. Ethiop., 2010
10.
Applications of Metal-Free 1,2,4-Triazole Derivatives in Materials Science
Diaz-Ortiz A., Prieto P., R. Carrillo J., Martin R., Torres I.
Current Organic Chemistry, 2015
11.
Triazoles and tetrazoles: Prime ligands to generate remarkable coordination materials
Aromí G., Barrios L.A., Roubeau O., Gamez P.
Coordination Chemistry Reviews, 2011
12.
Approches to the Synthesis of 1-substituted 1,2,4-Triazoles
F. V. Scriven E., Balasubramanian M., G. Keay J., Shobana N.
Heterocycles, 1994
13.
Synthesis of 3,4,5-Trisubstituted-1,2,4-triazoles
Moulin A., Bibian M., Blayo A., El Habnouni S., Martinez J., Fehrentz J.
Chemical Reviews, 2010
14.
Synthesis ofN-Substituted 1,2,4-Triazoles. A Review
Holm S.C., Straub B.F.
Organic Preparations and Procedures International, 2011
15.
Kaur P., Kaur R., Goswami M.
International Research Journal of Pharmacy, 2018
16.
A New Synthesis of 1-Aryl-1H-1, 2, 4-triazole-3-carboxylic Acid Esters
MATSUMOTO K., SUZUKI M., TOMIE M., YONEDA N., MIYOSHI M.
Synthesis, 1975
17.
Isocyanoacetate Derivatives: Synthesis, Reactivity, and Application
Gulevich A.V., Zhdanko A.G., Orru R.V., Nenajdenko V.G.
Chemical Reviews, 2010
19.
Flow synthesis of ethyl isocyanoacetate enabling the telescoped synthesis of 1,2,4-triazoles and pyrrolo-[1,2-c]pyrimidines
Baumann M., Rodriguez Garcia A.M., Baxendale I.R.
Organic and Biomolecular Chemistry, 2015
21.
10.1016/j.mencom.2019.11.016_bib0105
Mokrushin
Khimiya geterotsiklicheskikh diazosoedinenii (Chemistry of Heterocyclic Diazo Compounds), 2013
22.
Synthesis of 6,8-substituted derivatives of imidazo[5,1-c][1,2,4]triazines and 1,4-dihydroimidazo[5,1-c][1,2,4]triazin-4-ones
Bezmaternykh M.A., Mokrushin V.S., Pospelova T.A., El'tsov O.S.
Chemistry of Heterocyclic Compounds, 1998
23.
Alkyl 3-fluoroalkyl-3-oxopropionates in reactions with azolyldiazonium salts
Shchegol’kov E.V., Sadchikova E.V., Burgart Y.V., Saloutin V.I.
Russian Chemical Bulletin, 2008
24.
Interaction of 3,8-Disubstituted Imidazo-[5,1-C][1,2,4]Triazines with Nucleophiles**
Sadchikova E.V., Mokrushin* V.S.
Chemistry of Heterocyclic Compounds, 2014
25.
Synthesis and structure of 4-hydroxy-4-fluoroalkyl-1,4-dihydroimidazo[5,1-c][1,2,4]triazines
Shchegol’kov E.V., Sadchikova E.V., Burgart Y.V., Saloutin V.I.
Russian Journal of Organic Chemistry, 2009
29.
Synthesis of new 2-azaadenines and 2-azahypoxanthines from 4-diazo-4H-imidazoles
Andersen K.E., Pedersen E.B.
European Journal of Organic Chemistry, 1986
30.
Synthesis and properties of 5-diazoimidazoles and imidazolyl-5-diazonium salts
31.
Pyrazoles I. Synthesis of 4-Hydroxpyrazolo[3,4-d]-v-triazine A New Analog of Hypoxanthine
Cheng C.C., Robins R.K., Cheng K.C., Lin D.C.
Journal of Pharmaceutical Sciences, 1968
32.
3 The Medicinal Chemistry of 1,2,3-Triazines
Stevens M.F.
Progress in Medicinal Chemistry, 1976
33.
Synthesis of Potential Anticancer Agents. XXIX. 5-Diazoimidazole-4-carboxamide and 5-Diazo-v-triazole-4-carboxamide1,2
SHEALY Y.F., STRUCK R.F., HOLUM L.B., MONTGOMERY J.A.
Journal of Organic Chemistry, 1961