Home / Publications / Synthesis of dibenzo[b,g][1,5]diazoninedione and isoindolo[2,1-a]quinazoline derivatives

Synthesis of dibenzo[b,g][1,5]diazoninedione and isoindolo[2,1-a]quinazoline derivatives

Mehdi Bakavoli 1, 2
Mehdi Bakavoli
Abolghasem Davoodnia 2
Abolghasem Davoodnia
Majid M Heravi 1, 3
Majid M Heravi
Mohammad Rahimizadeh 1
Mohammad Rahimizadeh
Published 2006-01-31
CommunicationVolume 16, Issue 1, 29-30
12
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Bakavoli M. et al. Synthesis of dibenzo[b,g][1,5]diazoninedione and isoindolo[2,1-a]quinazoline derivatives // Mendeleev Communications. 2006. Vol. 16. No. 1. pp. 29-30.
GOST all authors (up to 50) Copy
Bakavoli M., Davoodnia A., Heravi M. M., Rahimizadeh M. Synthesis of dibenzo[b,g][1,5]diazoninedione and isoindolo[2,1-a]quinazoline derivatives // Mendeleev Communications. 2006. Vol. 16. No. 1. pp. 29-30.
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TY - JOUR
DO - 10.1070/MC2006v016n01ABEH002177
UR - https://mendcomm.colab.ws/publications/10.1070/MC2006v016n01ABEH002177
TI - Synthesis of dibenzo[b,g][1,5]diazoninedione and isoindolo[2,1-a]quinazoline derivatives
T2 - Mendeleev Communications
AU - Bakavoli, Mehdi
AU - Davoodnia, Abolghasem
AU - Heravi, Majid M
AU - Rahimizadeh, Mohammad
PY - 2006
DA - 2006/01/31
PB - Mendeleev Communications
SP - 29-30
IS - 1
VL - 16
ER -
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@article{2006_Bakavoli,
author = {Mehdi Bakavoli and Abolghasem Davoodnia and Majid M Heravi and Mohammad Rahimizadeh},
title = {Synthesis of dibenzo[b,g][1,5]diazoninedione and isoindolo[2,1-a]quinazoline derivatives},
journal = {Mendeleev Communications},
year = {2006},
volume = {16},
publisher = {Mendeleev Communications},
month = {Jan},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2006v016n01ABEH002177},
number = {1},
pages = {29--30},
doi = {10.1070/MC2006v016n01ABEH002177}
}
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Bakavoli, Mehdi, et al. “Synthesis of dibenzo[b,g][1,5]diazoninedione and isoindolo[2,1-a]quinazoline derivatives.” Mendeleev Communications, vol. 16, no. 1, Jan. 2006, pp. 29-30. https://mendcomm.colab.ws/publications/10.1070/MC2006v016n01ABEH002177.

Abstract

Starting from 2-aminobenzonitrile 1 and 2-chloromethylbenzoyl chloride 2, a new synthetic pathway to tetracyclic compound 6 is described. Reaction of 2-aminobenzamide 7 with compound 2 leads to the tricyclic ring system 9 which was easily converted to compound 6 in the presence of KOH in refluxing H2O–EtOH.

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