Synthesis of 3-Fluoropyrazolo[1,5-A]Pyridines by Fluorination of Methyl Pyrazolo[1,5-A]Pyridine-3-Carboxylates

Synthesis of 3-Fluoropyrazolo[1,5-A]Pyridines by Fluorination of Methyl Pyrazolo[1,5-A]Pyridine-3-Carboxylates Научная публикация

Журнал

Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353

Вых. Данные

Год: 2020, Том: 56, Номер: 7, Страницы: 957-960 Страниц : 4 DOI: 10.1007/s10593-020-02757-7

Ключевые слова

electrophilic fluorination; pyrazolo[1,5-a]pyridines; Selectfluor

Авторы

Alieva Sabina V. ^1,2 , Vorob’ev Aleksey Yu. ¹

Организации

1	(Scopus) N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 9 Akademika Lavrentieva Ave, Novosibirsk, 630090, Russian Federation
2	(Scopus) Novosibirsk State University, 1 Pirogova St, Novosibirsk, 630090, Russian Federation

[Figure not available: see fulltext.] The reaction of methyl esters of pyrazolo[1,5-a]pyridine-2,3-dicarboxylic and 2-phenylpyrazolo[1,5-a]pyridine-3-carboxylic acids with the fluorinating reagent Selectfluor gave 3-fluoropyrazolo[1,5-a]pyridine-2-carboxylic acid methyl ester and 3-fluoro-2-phenylpyrazolo- [1,5-a]pyridine. Monitoring the progress of the reaction by 1H NMR spectroscopy showed the formation of an intermediate fluorinecontaining σ-complex. © 2020, Springer Science+Business Media, LLC, part of Springer Nature.

Alieva S.V. , Vorob’ev A.Y.
Synthesis of 3-Fluoropyrazolo[1,5-A]Pyridines by Fluorination of Methyl Pyrazolo[1,5-A]Pyridine-3-Carboxylates
Chemistry of Heterocyclic Compounds. 2020. V.56. N7. P.957-960. DOI: 10.1007/s10593-020-02757-7 WOS Scopus РИНЦ OpenAlex

Опубликована в печати:	1 июл. 2020 г.
Опубликована online:	21 авг. 2020 г.

Web of science:	WOS:000561986600004
Scopus:	2-s2.0-85089751387
РИНЦ:	45375289
OpenAlex:	W3080489066

БД	Цитирований
Scopus	2
Web of science	1
РИНЦ	2
OpenAlex	3