Sciact
  • EN
  • RU

Transformations of 2-aminopyrimidines and their N-oxides under diazotization conditions Научная публикация

Журнал Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Вых. Данные Год: 1983, Том: 19, Номер: 1, Страницы: 91-95 Страниц : 5 DOI: 10.1007/BF00512824
Авторы Sedova V.F. 1 , Mustafina T.Yu. 1 , Krivopalov V.P. 1 , Mamaev V.P. 1
Организации
1 (Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR, Novosibirsk, 630090, Russian Federation

Реферат: The diazotization of 2-aminopyrimidines and their N-oxides in solutions with various acidities was studied. It is shown that the amino group in pyrimidine N-oxides is not diazotized in strongly acidic media and that bromination in the 5 position of the pyrimidine ring is observed in concentrated hydrobromic acid. When the reaction was carried out in moderately acidic media, it was possible to synthesize the difficult-to-obtain 2-halopyrimidine N-oxides. © 1983 Plenum Publishing Corporation.
Библиографическая ссылка: Sedova V.F. , Mustafina T.Y. , Krivopalov V.P. , Mamaev V.P.
Transformations of 2-aminopyrimidines and their N-oxides under diazotization conditions
Chemistry of Heterocyclic Compounds. 1983. V.19. N1. P.91-95. DOI: 10.1007/BF00512824 Scopus РИНЦ OpenAlex
Оригинальная: Sedova V.F. , Mustafina T.Y. , Krivopalov V.P. , Mamayev V.P.
TRANSFORMATIONS OF 2-AMINOPYRIMIDINES AND THEIR N-OXIDES IN DIAZOTIZATION REACTION
Химия гетероциклических соединений/Khimiya Geterotsiklicheskikh Soedinenii. 1983. N1. P.102-106. WOS
Даты:
Опубликована в печати: 1 янв. 1983 г.
Идентификаторы БД:
Scopus: 2-s2.0-34250144835
РИНЦ: 30901935
OpenAlex: W3170181503
Цитирование в БД:
БД Цитирований
Scopus 4
РИНЦ 4
OpenAlex 6
Альметрики: