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A reaction of hexafluoro-1,4-naphthoquinone with 2-aminopyridines

Ekaterina N Kudryavtseva 1
Ekaterina N Kudryavtseva
, 
Boris Valer'evich Lichitsky 1
Boris Valer'evich Lichitsky
, 
Eugene Viktorovich Tretyakov 1
Eugene Viktorovich Tretyakov
10.71267/mencom.7737
Published 2025-03-31
Communication , Volume 35, Issue 3, 258-260
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Kudryavtseva E. N., Lichitsky B. V., Tretyakov E. V. A reaction of hexafluoro-1,4-naphthoquinone with 2-aminopyridines // Mendeleev Communications. 2025. Vol. 35. No. 3. pp. 258-260.
GOST all authors (up to 50) Copy
Kudryavtseva E. N., Lichitsky B. V., Tretyakov E. V. A reaction of hexafluoro-1,4-naphthoquinone with 2-aminopyridines // Mendeleev Communications. 2025. Vol. 35. No. 3. pp. 258-260.
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TY - JOUR
DO - 10.71267/mencom.7737
UR - https://mendcomm.colab.ws/publications/10.71267/mencom.7737
TI - A reaction of hexafluoro-1,4-naphthoquinone with 2-aminopyridines
T2 - Mendeleev Communications
AU - Kudryavtseva, Ekaterina N
AU - Lichitsky, Boris Valer'evich
AU - Tretyakov, Eugene Viktorovich
PY - 2025
DA - 2025/03/31
PB - Mendeleev Communications
SP - 258-260
IS - 3
VL - 35
ER -
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@article{2025_Kudryavtseva,
author = {Ekaterina N Kudryavtseva and Boris Valer'evich Lichitsky and Eugene Viktorovich Tretyakov},
title = {A reaction of hexafluoro-1,4-naphthoquinone with 2-aminopyridines},
journal = {Mendeleev Communications},
year = {2025},
volume = {35},
publisher = {Mendeleev Communications},
month = {Mar},
url = {https://mendcomm.colab.ws/publications/10.71267/mencom.7737},
number = {3},
pages = {258--260},
doi = {10.71267/mencom.7737}
}
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Kudryavtseva, Ekaterina N., et al. “A reaction of hexafluoro-1,4-naphthoquinone with 2-aminopyridines.” Mendeleev Communications, vol. 35, no. 3, Mar. 2025, pp. 258-260. https://mendcomm.colab.ws/publications/10.71267/mencom.7737.

Keywords

2-a]pyridine- 5
2-aminopyridines
2':4
5]imidazo[1
6-diones
condensation
fused heterocyclic quinones
naphtho[1'
naphthoquinones
organofluorine compounds.

Abstract

A reaction of hexafluoro-1,4-naphthoquinone with 2-aminopyridines leads to fluorinated naphtho[1',2':4,5]imidazo[1,2-a]pyridine-5,6-diones. Advantages of the proposed one-step procedure are easily available starting materials, atom economy, and simple isolation of products without chromatographic purification.

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