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Cyclocondensation of anthranilic acids with generated in situ methyl pyrimidine-2-carbimidate in the synthesis of 2-(pyrimidin-2-yl)quinazolin-4(3H)-ones. / Valieva, M.; Rybakova, S.; Kudryashova, E. et al.
In: Russian Chemical Bulletin, Vol. 72, No. 12, 2023, p. 2974-2978.

Research output: Contribution to journal › Article › peer-review

Harvard

Valieva, M, Rybakova, S, Kudryashova, E, Rahman, M, Santra, S, Kopchuk, D, Nosova, E, Gorbunov, E, Zyryanov, G & Chupakhin, O 2023, 'Cyclocondensation of anthranilic acids with generated in situ methyl pyrimidine-2-carbimidate in the synthesis of 2-(pyrimidin-2-yl)quinazolin-4(3H)-ones', Russian Chemical Bulletin, vol. 72, no. 12, pp. 2974-2978. https://doi.org/10.1007/s11172-023-4108-3

APA

Valieva, M., Rybakova, S., Kudryashova, E., Rahman, M., Santra, S., Kopchuk, D., Nosova, E., Gorbunov, E., Zyryanov, G., & Chupakhin, O. (2023). Cyclocondensation of anthranilic acids with generated in situ methyl pyrimidine-2-carbimidate in the synthesis of 2-(pyrimidin-2-yl)quinazolin-4(3H)-ones. Russian Chemical Bulletin, 72(12), 2974-2978. https://doi.org/10.1007/s11172-023-4108-3

Vancouver

Valieva M, Rybakova S, Kudryashova E, Rahman M, Santra S, Kopchuk D et al. Cyclocondensation of anthranilic acids with generated in situ methyl pyrimidine-2-carbimidate in the synthesis of 2-(pyrimidin-2-yl)quinazolin-4(3H)-ones. Russian Chemical Bulletin. 2023;72(12):2974-2978. doi: 10.1007/s11172-023-4108-3

Author

Valieva, M. ; Rybakova, S. ; Kudryashova, E. et al. / Cyclocondensation of anthranilic acids with generated in situ methyl pyrimidine-2-carbimidate in the synthesis of 2-(pyrimidin-2-yl)quinazolin-4(3H)-ones. In: Russian Chemical Bulletin. 2023 ; Vol. 72, No. 12. pp. 2974-2978.

BibTeX

@article{559a22895ed049739edf92292430b6d6,
title = "Cyclocondensation of anthranilic acids with generated in situ methyl pyrimidine-2-carbimidate in the synthesis of 2-(pyrimidin-2-yl)quinazolin-4(3H)-ones",
abstract = "The possibilities of the synthesis of new derivatives of quinazolin-4(3H)-ones by the reactions of different functionalized anthranilic acids with imino ether generated in situ from 2-cyanopyrimidine were studied. It was shown that the presence of different substituents in the anthranilic acids, including halogen atoms, methoxy and methyl groups, did not interfere with the reaction. {\textcopyright} 2023, Springer Science+Business Media LLC.",
author = "M. Valieva and S. Rybakova and E. Kudryashova and M. Rahman and S. Santra and D. Kopchuk and E. Nosova and E. Gorbunov and G. Zyryanov and O. Chupakhin",
note = "This work was financially supported by the Russian Science Foundation (Project No. 23-13-00318) and the Council on Grants at the President of the Russian Federation (Project No. NSh-1223.2022.1.3).",
year = "2023",
doi = "10.1007/s11172-023-4108-3",
language = "English",
volume = "72",
pages = "2974--2978",
journal = "Russian Chemical Bulletin",
issn = "1066-5285",
publisher = "Springer",
number = "12",

}

RIS

TY - JOUR

T1 - Cyclocondensation of anthranilic acids with generated in situ methyl pyrimidine-2-carbimidate in the synthesis of 2-(pyrimidin-2-yl)quinazolin-4(3H)-ones

AU - Valieva, M.

AU - Rybakova, S.

AU - Kudryashova, E.

AU - Rahman, M.

AU - Santra, S.

AU - Kopchuk, D.

AU - Nosova, E.

AU - Gorbunov, E.

AU - Zyryanov, G.

AU - Chupakhin, O.

N1 - This work was financially supported by the Russian Science Foundation (Project No. 23-13-00318) and the Council on Grants at the President of the Russian Federation (Project No. NSh-1223.2022.1.3).

PY - 2023

Y1 - 2023

N2 - The possibilities of the synthesis of new derivatives of quinazolin-4(3H)-ones by the reactions of different functionalized anthranilic acids with imino ether generated in situ from 2-cyanopyrimidine were studied. It was shown that the presence of different substituents in the anthranilic acids, including halogen atoms, methoxy and methyl groups, did not interfere with the reaction. © 2023, Springer Science+Business Media LLC.

AB - The possibilities of the synthesis of new derivatives of quinazolin-4(3H)-ones by the reactions of different functionalized anthranilic acids with imino ether generated in situ from 2-cyanopyrimidine were studied. It was shown that the presence of different substituents in the anthranilic acids, including halogen atoms, methoxy and methyl groups, did not interfere with the reaction. © 2023, Springer Science+Business Media LLC.

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85183640814

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=001154671000006

U2 - 10.1007/s11172-023-4108-3

DO - 10.1007/s11172-023-4108-3

M3 - Article

VL - 72

SP - 2974

EP - 2978

JO - Russian Chemical Bulletin

JF - Russian Chemical Bulletin

SN - 1066-5285

IS - 12

ER -

ID: 52286986