Solvent-Free Reaction of 3,6-Diaryl-1,2,4-triazine-5-carbonitriles with 2-Amino-4-aryloxazoles

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Solvent-Free Reaction of 3,6-Diaryl-1,2,4-triazine-5-carbonitriles with 2-Amino-4-aryloxazoles. / Rammohan, A.; Shtaitz, Ya. K.; Ladin, E. D. et al.
In: Russian Journal of General Chemistry, Vol. 93, No. 2, 2023, p. 263-267.

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

BibTeX

@article{160addf0494247bcad476a57f6fc97cf,

title = "Solvent-Free Reaction of 3,6-Diaryl-1,2,4-triazine-5-carbonitriles with 2-Amino-4-aryloxazoles",

abstract = "Solvent-free reaction of 3,6-diaryl-1,2,4-triazine-5-carbonitriles with 2-amino-4-aryloxazoles was studied. In this case, the formation of 3- and 4-aryl-substituted pyridines (two isomeric products) in yields up to 20 and 27%, respectively, was found. This result is different from that for the reaction of 3-(2-pyridyl)-1,2,4-triazine-5-carbonitriles with these substrates. Thus, in this case, 2-amino-4-aryloxazoles act as synthetic analogues of arylacetylenes. {\textcopyright} 2023, Pleiades Publishing, Ltd.",

author = "A. Rammohan and Shtaitz, {Ya. K.} and Ladin, {E. D.} and Krinochkin, {A. P.} and Slepukhin, {P. A.} and Sharutin, {V. V.} and Sharafieva, {E. R.} and Pospelova, {T. A.} and Kopchuk, {D. S.} and Zyryanov, {G. V.}",

note = "The work was supported by the Council for Grants of the President of the Russian Federation (grant no. MK-320.2021.1.3), as well as within the framework of the governmental task (topic AAAA-A19-119011790132-7).",

year = "2023",

doi = "10.1134/S1070363223020056",

language = "English",

volume = "93",

pages = "263--267",

journal = "Russian Journal of General Chemistry",

issn = "1070-3632",

publisher = "Maik Nauka-Interperiodica Publishing",

number = "2",

}

RIS

TY - JOUR

T1 - Solvent-Free Reaction of 3,6-Diaryl-1,2,4-triazine-5-carbonitriles with 2-Amino-4-aryloxazoles

AU - Rammohan, A.

AU - Shtaitz, Ya. K.

AU - Ladin, E. D.

AU - Krinochkin, A. P.

AU - Slepukhin, P. A.

AU - Sharutin, V. V.

AU - Sharafieva, E. R.

AU - Pospelova, T. A.

AU - Kopchuk, D. S.

AU - Zyryanov, G. V.

N1 - The work was supported by the Council for Grants of the President of the Russian Federation (grant no. MK-320.2021.1.3), as well as within the framework of the governmental task (topic AAAA-A19-119011790132-7).

PY - 2023

Y1 - 2023

N2 - Solvent-free reaction of 3,6-diaryl-1,2,4-triazine-5-carbonitriles with 2-amino-4-aryloxazoles was studied. In this case, the formation of 3- and 4-aryl-substituted pyridines (two isomeric products) in yields up to 20 and 27%, respectively, was found. This result is different from that for the reaction of 3-(2-pyridyl)-1,2,4-triazine-5-carbonitriles with these substrates. Thus, in this case, 2-amino-4-aryloxazoles act as synthetic analogues of arylacetylenes. © 2023, Pleiades Publishing, Ltd.

AB - Solvent-free reaction of 3,6-diaryl-1,2,4-triazine-5-carbonitriles with 2-amino-4-aryloxazoles was studied. In this case, the formation of 3- and 4-aryl-substituted pyridines (two isomeric products) in yields up to 20 and 27%, respectively, was found. This result is different from that for the reaction of 3-(2-pyridyl)-1,2,4-triazine-5-carbonitriles with these substrates. Thus, in this case, 2-amino-4-aryloxazoles act as synthetic analogues of arylacetylenes. © 2023, Pleiades Publishing, Ltd.

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85151485700

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000984102600005

U2 - 10.1134/S1070363223020056

DO - 10.1134/S1070363223020056

M3 - Article

VL - 93

SP - 263

EP - 267

JO - Russian Journal of General Chemistry

JF - Russian Journal of General Chemistry

SN - 1070-3632

IS - 2

ER -

ID: 37143892