Alkylation of 2-(hydroxyimino)-5H-[1,3]thiazolo[3,2-a]-pyrimidin-3(2H)-ones
- Авторлар: Lashmanova E.A.1, Larina V.S.1, Shiryaev A.K.1
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Мекемелер:
- Samara State Technical University
- Шығарылым: Том 53, № 8 (2017)
- Беттер: 1249-1252
- Бөлім: Article
- URL: https://journals.rcsi.science/1070-4280/article/view/216742
- DOI: https://doi.org/10.1134/S1070428017080152
- ID: 216742
Дәйексөз келтіру
Аннотация
Alkylation products were obtained from ethyl 2-(hydroxyimino)-7-methyl-3-oxo-5-aryl-2,3- dihydro-5H-[1,3]thiazolo[3,2-a]pyrimidin-6-carboxylates at the treatment with alkyl halides, dimethyl sulfate, and diazomethane. Diazomethane alkylated the initial substrate at the oxygen atom of the carbonyl group of the thiazolidine fragment, the other reagents, at the oxygen atom of the hydroxyimino group.
Авторлар туралы
E. Lashmanova
Samara State Technical University
Хат алмасуға жауапты Автор.
Email: lashmanovaea@gmail.com
Ресей, Molodogvardeiskaya ul. 244, Samara, 443100
V. Larina
Samara State Technical University
Email: lashmanovaea@gmail.com
Ресей, Molodogvardeiskaya ul. 244, Samara, 443100
A. Shiryaev
Samara State Technical University
Email: lashmanovaea@gmail.com
Ресей, Molodogvardeiskaya ul. 244, Samara, 443100
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