Russian Journal of Organic Chemistry, volume 58, issue 2, pages 244-248

Synthesis of Hydantoins Spiro-Annulated to the Pyrrole Ring, by the Reaction of Pyrrolo[1,2-c][4,1]benzoxazepinetriones with Urea and Thiourea

Publication typeJournal Article
Publication date2022-02-01
Quartile SCImago
Q4
Quartile WOS
Q4
Impact factor0.8
ISSN10704280, 16083393
Organic Chemistry
Abstract
The reaction of 3-aroylpyrrolo[1,2-c][4,1]benzoxazepine-1,2,4-triones with urea and thiourea leads to the formation of 9-aroyl-8-hydroxy-6-[2-(hydroxymethyl)phenyl]-1,3,6-triazaspiro[4.4]-non-8-ene-2,4,7-triones and 9-aroyl-8-hydroxy-6-[2-(hydroxymethyl)phenyl]-2-thioxo-1,3,6-triazaspiro[4.4]non-8-ene-4,7-diones, respectively. The described reaction is a convenient method for the synthesis of the hardly accessible 1,3,6-triazaspiro[4.4]nonenone system (hydantoins spiro-annulated to the pyrrole ring).
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Maslivets A. A. et al. Synthesis of Hydantoins Spiro-Annulated to the Pyrrole Ring, by the Reaction of Pyrrolo[1,2-c][4,1]benzoxazepinetriones with Urea and Thiourea // Russian Journal of Organic Chemistry. 2022. Vol. 58. No. 2. pp. 244-248.
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Maslivets A. A., Andreeva A. A., Dmitriev M. V., Maslivets A. N. Synthesis of Hydantoins Spiro-Annulated to the Pyrrole Ring, by the Reaction of Pyrrolo[1,2-c][4,1]benzoxazepinetriones with Urea and Thiourea // Russian Journal of Organic Chemistry. 2022. Vol. 58. No. 2. pp. 244-248.
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TY - JOUR
DO - 10.1134/S1070428022020129
UR - https://doi.org/10.1134%2FS1070428022020129
TI - Synthesis of Hydantoins Spiro-Annulated to the Pyrrole Ring, by the Reaction of Pyrrolo[1,2-c][4,1]benzoxazepinetriones with Urea and Thiourea
T2 - Russian Journal of Organic Chemistry
AU - Maslivets, Anna A
AU - Andreeva, A A
AU - Dmitriev, Maksim V
AU - Maslivets, Andrey N
PY - 2022
DA - 2022/02/01 00:00:00
PB - Pleiades Publishing
SP - 244-248
IS - 2
VL - 58
SN - 1070-4280
SN - 1608-3393
ER -
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@article{2022_Maslivets,
author = {Anna A Maslivets and A A Andreeva and Maksim V Dmitriev and Andrey N Maslivets},
title = {Synthesis of Hydantoins Spiro-Annulated to the Pyrrole Ring, by the Reaction of Pyrrolo[1,2-c][4,1]benzoxazepinetriones with Urea and Thiourea},
journal = {Russian Journal of Organic Chemistry},
year = {2022},
volume = {58},
publisher = {Pleiades Publishing},
month = {feb},
url = {https://doi.org/10.1134%2FS1070428022020129},
number = {2},
pages = {244--248},
doi = {10.1134/S1070428022020129}
}
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Maslivets, Anna A., et al. “Synthesis of Hydantoins Spiro-Annulated to the Pyrrole Ring, by the Reaction of Pyrrolo[1,2-c][4,1]benzoxazepinetriones with Urea and Thiourea.” Russian Journal of Organic Chemistry, vol. 58, no. 2, Feb. 2022, pp. 244-248. https://doi.org/10.1134%2FS1070428022020129.
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