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Unusual reactions of 4,6-dichloro-5-nitropyrimidine with C-nucleophiles

Yurii Alexeevich Azev 1
Yurii Alexeevich Azev
, 
Thomas Duelcks 2
Thomas Duelcks
, 
Enno Lork 2
Enno Lork
, 
Detlef Gabel 2
Detlef Gabel
10.1070/MC2005v015n05ABEH002156
Published 2005-09-09
Communication , Volume 15, Issue 5, 193-196
3
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Azev Y. A. et al. Unusual reactions of 4,6-dichloro-5-nitropyrimidine with C-nucleophiles // Mendeleev Communications. 2005. Vol. 15. No. 5. pp. 193-196.
GOST all authors (up to 50) Copy
Azev Y. A., Duelcks T., Lork E., Gabel D. Unusual reactions of 4,6-dichloro-5-nitropyrimidine with C-nucleophiles // Mendeleev Communications. 2005. Vol. 15. No. 5. pp. 193-196.
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TY - JOUR
DO - 10.1070/MC2005v015n05ABEH002156
UR - https://mendcomm.colab.ws/publications/10.1070/MC2005v015n05ABEH002156
TI - Unusual reactions of 4,6-dichloro-5-nitropyrimidine with C-nucleophiles
T2 - Mendeleev Communications
AU - Azev, Yurii Alexeevich
AU - Duelcks, Thomas
AU - Lork, Enno
AU - Gabel, Detlef
PY - 2005
DA - 2005/09/09
PB - Mendeleev Communications
SP - 193-196
IS - 5
VL - 15
ER -
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@article{2005_Azev,
author = {Yurii Alexeevich Azev and Thomas Duelcks and Enno Lork and Detlef Gabel},
title = {Unusual reactions of 4,6-dichloro-5-nitropyrimidine with C-nucleophiles},
journal = {Mendeleev Communications},
year = {2005},
volume = {15},
publisher = {Mendeleev Communications},
month = {Sep},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2005v015n05ABEH002156},
number = {5},
pages = {193--196},
doi = {10.1070/MC2005v015n05ABEH002156}
}
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Azev, Yurii Alexeevich, et al. “Unusual reactions of 4,6-dichloro-5-nitropyrimidine with C-nucleophiles.” Mendeleev Communications, vol. 15, no. 5, Sep. 2005, pp. 193-196. https://mendcomm.colab.ws/publications/10.1070/MC2005v015n05ABEH002156.

Abstract

The interaction of 4,6-dichloro-5-nitropyrimidine 1 with 1-phenyl-3-methylpyrazol-5-one led to the 4,6-dipyrazolyl derivatives of 5-nitropyrimidine 2 and dipyrazolylmethane 3; 2-methylindole reacts with 1 to form diindolylmethane 4 and trisindolylmethane 5; 1,3-dimethylbarbituric acid displaces an indolyl residue in diindolylmethane 4 to form diheterylmethane 6.

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