Synthesis and biological activity of oxindolylidene derivatives of imidazo[4,5-e]thiazolo[3,2-b]-1,2,4-triazin-7-ones and imidazo[4,5-e]thiazolo[2,3-с]-1,2,4-triazin-8-ones
- 作者: Izmest’ev A.N.1, Gazieva G.A.1, Kulikov A.S.1, Anikina L.V.2, Kolotyrkina N.G.1, Kravchenko A.N.1
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隶属关系:
- Zelinskii Institute of Organic Chemistry
- Institute of Physiologically Active Substances
- 期: 卷 53, 编号 5 (2017)
- 页面: 753-763
- 栏目: Article
- URL: https://journal-vniispk.ru/1070-4280/article/view/216239
- DOI: https://doi.org/10.1134/S1070428017050177
- ID: 216239
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详细
Reactions of 1,3-dialkyl-2-thioxo-1,2,3,3a,9,9a-hexahydroimidazo[4,5-e]thiazolo[3,2-b]-1,2,4-triazin-7(6H)-ones with isatin and its derivatives under base catalysis conditions lead to the corresponding 1,3-dialkyl-6(7)-(2-oxoindolin-3-ylidene)derivatives of 2-thioxo-1,2,3,3a,9,9a-hexahydroimidazo[4,5-e]thiazolo[3,2-b]-1,2,4-triazin-7(6H)-one or 2-thioxo-1,2,3,3a,4,9a-hexahydroimidazo[4,5-e]thiazolo[2,3-c]-1,2,4-triazin-8(7H)-one resulting from the aldol-crotonic condensation and skeletal amidine rearrangement of the thiazolotriazine fragment, depending on the amount of added alkali.
作者简介
A. Izmest’ev
Zelinskii Institute of Organic Chemistry
Email: gaz@ioc.ac.ru
俄罗斯联邦, Leninskii pr. 47, Moscow, 119991
G. Gazieva
Zelinskii Institute of Organic Chemistry
编辑信件的主要联系方式.
Email: gaz@ioc.ac.ru
俄罗斯联邦, Leninskii pr. 47, Moscow, 119991
A. Kulikov
Zelinskii Institute of Organic Chemistry
Email: gaz@ioc.ac.ru
俄罗斯联邦, Leninskii pr. 47, Moscow, 119991
L. Anikina
Institute of Physiologically Active Substances
Email: gaz@ioc.ac.ru
俄罗斯联邦, Chernogolovka, Moscow oblast
N. Kolotyrkina
Zelinskii Institute of Organic Chemistry
Email: gaz@ioc.ac.ru
俄罗斯联邦, Leninskii pr. 47, Moscow, 119991
A. Kravchenko
Zelinskii Institute of Organic Chemistry
Email: gaz@ioc.ac.ru
俄罗斯联邦, Leninskii pr. 47, Moscow, 119991
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