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A new synthesis of 2-(aminoalkyl)-1,2,4-triazolo[1,5-a]pyrimidines

Mikhail Avramovich Prezent 1
Mikhail Avramovich Prezent
, 
Elena Dmitrievna Daeva 1
Elena Dmitrievna Daeva
, 
Sergey Viktorovich Baranin 1
Sergey Viktorovich Baranin
, 
Igor Viktorovich Zavarzin 1
Igor Viktorovich Zavarzin
10.1016/j.mencom.2017.03.021
Published 2017-02-27
Communication , Volume 27, Issue 2, 169-171
10
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Prezent M. A. et al. A new synthesis of 2-(aminoalkyl)-1,2,4-triazolo[1,5-a]pyrimidines // Mendeleev Communications. 2017. Vol. 27. No. 2. pp. 169-171.
GOST all authors (up to 50) Copy
Prezent M. A., Daeva E. D., Baranin S. V., Zavarzin I. V. A new synthesis of 2-(aminoalkyl)-1,2,4-triazolo[1,5-a]pyrimidines // Mendeleev Communications. 2017. Vol. 27. No. 2. pp. 169-171.
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TY - JOUR
DO - 10.1016/j.mencom.2017.03.021
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2017.03.021
TI - A new synthesis of 2-(aminoalkyl)-1,2,4-triazolo[1,5-a]pyrimidines
T2 - Mendeleev Communications
AU - Prezent, Mikhail Avramovich
AU - Daeva, Elena Dmitrievna
AU - Baranin, Sergey Viktorovich
AU - Zavarzin, Igor Viktorovich
PY - 2017
DA - 2017/02/27
PB - Mendeleev Communications
SP - 169-171
IS - 2
VL - 27
ER -
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@article{2017_Prezent,
author = {Mikhail Avramovich Prezent and Elena Dmitrievna Daeva and Sergey Viktorovich Baranin and Igor Viktorovich Zavarzin},
title = {A new synthesis of 2-(aminoalkyl)-1,2,4-triazolo[1,5-a]pyrimidines},
journal = {Mendeleev Communications},
year = {2017},
volume = {27},
publisher = {Mendeleev Communications},
month = {Feb},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2017.03.021},
number = {2},
pages = {169--171},
doi = {10.1016/j.mencom.2017.03.021}
}
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MLA Copy
Prezent, Mikhail Avramovich, et al. “A new synthesis of 2-(aminoalkyl)-1,2,4-triazolo[1,5-a]pyrimidines.” Mendeleev Communications, vol. 27, no. 2, Feb. 2017, pp. 169-171. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2017.03.021.

Abstract

Nickel(ii) acetylacetonate-promoted cycloaddition between Boc-protected amino acid hydrazides and benzoylcyanamide followed by deprotection gives 2-amino-5-aminoalkyl-1,2,4-triazoles, whose reaction with 1,3-dielectrophiles affords the title compounds.

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