Nitropyrazoles 22. On reactivity of 3,5-dinitro-4-(phenylsulfonyl)pyrazole and its N-methyl derivative Научная публикация
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Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285 |
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| Вых. Данные | Год: 2012, Том: 61, Номер: 2, Страницы: 469-471 Страниц : 3 DOI: 10.1007/s11172-012-0067-9 | ||
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Реферат:
3,5-Dinitro-4-(phenylsulfonyl)pyrazole (5) obtained by oxidation of 3,5-dinitro-4-(phenylthio)pyrazole with 30% H2O2 in AcOH was involved into nucleophilic substitution reaction with thiophenol, which proceeded with substitution of the phenylsulfonyl group at position 4. N-Methyl-3,5-dinitro-4-(phenylsulfonyl)pyrazole obtained by methylation of 5 with dimethyl sulfate was involved into nucleophilic substitution reaction with thiophenol, p-bromophenol, and morpholine with the regioselective substitution of the nitro group at position 5 to form 5-R-3-nitro-4-(phenylsulfonyl)pyrazoles.
Библиографическая ссылка:
Vatsadze I.A.
, Dalinger I.L.
, Shkineva T.K.
, Popova G.P.
, Shevelev S.A.
Nitropyrazoles 22. On reactivity of 3,5-dinitro-4-(phenylsulfonyl)pyrazole and its N-methyl derivative
Russian Chemical Bulletin. 2012. V.61. N2. P.469-471. DOI: 10.1007/s11172-012-0067-9 WOS Scopus OpenAlex
Nitropyrazoles 22. On reactivity of 3,5-dinitro-4-(phenylsulfonyl)pyrazole and its N-methyl derivative
Russian Chemical Bulletin. 2012. V.61. N2. P.469-471. DOI: 10.1007/s11172-012-0067-9 WOS Scopus OpenAlex
Идентификаторы БД:
| ≡ Web of science: | WOS:000312068000036 |
| ≡ Scopus: | 2-s2.0-84877041737 |
| ≡ OpenAlex: | W1982678937 |