, volume 33 , issue 5 , pages 650-652

Regioselective synthesis of 2-(1H-benzimidazol-1-yl)-5-nitro- and 2-(5-nitro-1H-benzimidazol-1-yl)anilines

Roman S Begunov ¹

Anna V. Chetvertakova ¹

Margarita E. Neganova ^{2, 3}

Hide authors affiliations Show authors affiliations: 3 affiliations

P. G. Demidov Yaroslavl State University, 150003, Yaroslavl, Russian Federation |

A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 119334, Moscow, Russian Federation |

Institute of Physiologically Active Compounds, Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, 142432, Chernogolovka, Moscow Region, Russian Federation

Institute of Physiologically Active Compounds of the Russian Academy of Science

Federal Research Center of Problem of Chemical Physics and Medicinal Chemistry RAS

Publication type: Journal Article

Publication date: 2023-09-01

OOO Zhurnal "Mendeleevskie Soobshcheniya"

Mendeleev Communications

scimago Q3

wos Q3

SJR: 0.305

CiteScore: 3.0

Impact factor: 1.7

ISSN: 09599436, 1364551X

DOI: 10.1016/j.mencom.2023.09.020

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General Chemistry

Abstract

The efficiency of two strategies for the synthesis of N-(2-aminophenyl)-5-nitrobenzimidazole derivatives was studied. The promising route involves the stages of 1-(2,4-dinitro-phenyl)-1H-benzimidazole monoreduction at 2-positioned nitro group and tandem conversion involving recyclization of the intermediate N-(2-amino-4-nitrophenyl)-5-nitrobenz-imidazole.

Found

1 citation

Semenov Artem

18 publications, 137 citations

h-index: 5

Saint Petersburg State University

Research interests

Coordination Chemistry

Luminescent materials

Medicinal Chemistry

Organic Chemistry

1 citation

Baykov Sergey

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PhD in Chemistry

99 publications, 1 347 citations, 15 reviews

h-index: 21

Saint Petersburg State University

1 citation

Presnukhina Sofia

14 publications, 145 citations

h-index: 6

Yaroslavl State Pedagogical University

Saint Petersburg State University

Research interests

Heterocyclic compounds

Organic Chemistry

Organic synthesis

1 citation

Shetnev Anton

PhD in Chemistry

79 publications, 769 citations

h-index: 15

Moscow Institute of Physics and Technology

Yaroslavl State Medical University

Yaroslavl State Pedagogical University

1 citation

Volobueva Aleksandrina

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48 publications, 320 citations

h-index: 12

Saint-Petersburg Pasteur Institute

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Begunov R. S. et al. Regioselective synthesis of 2-(1H-benzimidazol-1-yl)-5-nitro- and 2-(5-nitro-1H-benzimidazol-1-yl)anilines // Mendeleev Communications. 2023. Vol. 33. No. 5. pp. 650-652.

GOST all authors (up to 50) Copy

Begunov R. S., Chetvertakova A. V., E. Neganova M. Regioselective synthesis of 2-(1H-benzimidazol-1-yl)-5-nitro- and 2-(5-nitro-1H-benzimidazol-1-yl)anilines // Mendeleev Communications. 2023. Vol. 33. No. 5. pp. 650-652.

RIS |

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RIS Copy

TY - JOUR

DO - 10.1016/j.mencom.2023.09.020

UR - https://doi.org/10.1016/j.mencom.2023.09.020

TI - Regioselective synthesis of 2-(1H-benzimidazol-1-yl)-5-nitro- and 2-(5-nitro-1H-benzimidazol-1-yl)anilines

T2 - Mendeleev Communications

AU - Begunov, Roman S

AU - Chetvertakova, Anna V.

AU - E. Neganova, Margarita

PY - 2023

DA - 2023/09/01

PB - OOO Zhurnal "Mendeleevskie Soobshcheniya"

SP - 650-652

IS - 5

VL - 33

SN - 0959-9436

SN - 1364-551X

ER -

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@article{2023_Begunov,

author = {Roman S Begunov and Anna V. Chetvertakova and Margarita E. Neganova},

title = {Regioselective synthesis of 2-(1H-benzimidazol-1-yl)-5-nitro- and 2-(5-nitro-1H-benzimidazol-1-yl)anilines},

journal = {Mendeleev Communications},

year = {2023},

volume = {33},

publisher = {OOO Zhurnal "Mendeleevskie Soobshcheniya"},

month = {sep},

url = {https://doi.org/10.1016/j.mencom.2023.09.020},

number = {5},

pages = {650--652},

doi = {10.1016/j.mencom.2023.09.020}

}

MLA

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Begunov, Roman S., et al. “Regioselective synthesis of 2-(1H-benzimidazol-1-yl)-5-nitro- and 2-(5-nitro-1H-benzimidazol-1-yl)anilines.” Mendeleev Communications, vol. 33, no. 5, Sep. 2023, pp. 650-652. https://doi.org/10.1016/j.mencom.2023.09.020.