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Nucleophilic substitution of hydrogen in 3,6-diphenyl-1,2,4-triazine 4-oxide

Yurii Alexeevich Azev 1
Yurii Alexeevich Azev
, 
Hans Neunhoeffer 2
Hans Neunhoeffer
, 
Sergei Victorovich Shorshnev 1
Sergei Victorovich Shorshnev
1 Ural Scientific Research Institute of Technology of Medical Preparations, Ekaterinburg, Russian Federation
10.1070/MC1996v006n03ABEH000607
Published 1996-06-30
Communication , Volume 6, Issue 3, 116-118
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Azev Y. A., Neunhoeffer H., Shorshnev S. V. Nucleophilic substitution of hydrogen in 3,6-diphenyl-1,2,4-triazine 4-oxide // Mendeleev Communications. 1996. Vol. 6. No. 3. pp. 116-118.
GOST all authors (up to 50) Copy
Azev Y. A., Neunhoeffer H., Shorshnev S. V. Nucleophilic substitution of hydrogen in 3,6-diphenyl-1,2,4-triazine 4-oxide // Mendeleev Communications. 1996. Vol. 6. No. 3. pp. 116-118.
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TY - JOUR
DO - 10.1070/MC1996v006n03ABEH000607
UR - https://mendcomm.colab.ws/publications/10.1070/MC1996v006n03ABEH000607
TI - Nucleophilic substitution of hydrogen in 3,6-diphenyl-1,2,4-triazine 4-oxide
T2 - Mendeleev Communications
AU - Azev, Yurii Alexeevich
AU - Neunhoeffer, Hans
AU - Shorshnev, Sergei Victorovich
PY - 1996
DA - 1996/06/30
PB - Mendeleev Communications
SP - 116-118
IS - 3
VL - 6
ER -
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@article{1996_Azev,
author = {Yurii Alexeevich Azev and Hans Neunhoeffer and Sergei Victorovich Shorshnev},
title = {Nucleophilic substitution of hydrogen in 3,6-diphenyl-1,2,4-triazine 4-oxide},
journal = {Mendeleev Communications},
year = {1996},
volume = {6},
publisher = {Mendeleev Communications},
month = {Jun},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1996v006n03ABEH000607},
number = {3},
pages = {116--118},
doi = {10.1070/MC1996v006n03ABEH000607}
}
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Azev, Yurii Alexeevich, et al. “Nucleophilic substitution of hydrogen in 3,6-diphenyl-1,2,4-triazine 4-oxide.” Mendeleev Communications, vol. 6, no. 3, Jun. 1996, pp. 116-118. https://mendcomm.colab.ws/publications/10.1070/MC1996v006n03ABEH000607.

Abstract

Reactions of 3,6-diphenyl-l,2,4-triazine 4-oxide 1 with indoles 2a,b in the presence of acid give the products of substitution of the H(5) atom, 5-(indolyl-3)-l,2,4-triazines 3a,b; the reaction of 1 with CH-acids in the presence of triethylamine also yields substitution products 5, and the derivative of ditriazinylmethane 6 was isolated along with product 5 in the reaction of 1 with acetyl- and benzoylacetone.

References

2.
Azev Y.A., Neunhoeffer H., Foro S., Lindner H.J., Shorshnev S.V.
Mendeleev Communications, 1995
3.
10.1070/MC1996v006n03ABEH000607_bib3
Azev
Khim. Farm. Zh., 1985
4.
10.1070/MC1996v006n03ABEH000607_bib4
Katritzky
Chemistry of Heterocydic N-Oxides, 1971