FEATURES OF (BENZO)IMIDAZO[2,1-B][1,3]THIAZINE MEZYLATES REACTION WITH NUCLEOPHILIC REAGENTS

被引:0
|
作者
Slyvka, Nataliia [1 ]
Saliyeva, Lesya [1 ]
Litvinchuk, Mariia [2 ]
Shishkina, Svitlana [3 ]
Vovk, Mykhailo [2 ]
机构
[1] Lesya Ukrainka Volyn Natl Univ, Dept Organ Chem & Pharm, Volya Ave 13, UA-43025 Lutsk, Ukraine
[2] Natl Acad Sci Ukraine, Inst Organ Chem, Dept Funct Heterocycl Syst, Acad Kuharya St, UA-02660 Kiev, Ukraine
[3] Natl Acad Sci Ukraine, SSI Inst Single Crystals, Dept Xray Diffract Study & Quantum Chem, Nauka Ave 60, UA-61000 Kharkiv, Ukraine
来源
CHEMISTRY & CHEMICAL TECHNOLOGY | 2023年 / 17卷 / 03期
关键词
nucleo-philic substitution reaction; elimination reaction; thio (isothio)cyanato and azido derivatives; (benzo)imidazo[2,1-b][1,3]thiazines; ANALOGS;
D O I
10.23939/chcht17.03.542
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Peculiarities of the course of the methanesulfoderivatives of (benzo)imidazo[2,1-b][1,3]thiazines reactions with a number of nucleophilic reagents were studied. It was determined that they react nonselectively with potassium thiocyanate to form a mixture of thio-and isothiocyanate derivatives. When interacting with sodium azide, nucleophilic substitution competes with an elimina-tion reaction. The latter is dominant in the reaction with sodium cyanide. The spatial structure of one of the isomer elimination products, 4H-benzo[4,5]imidazo[2,1-b][1,3] thiazine, was established by X-ray structural analysis.
引用
收藏
页码:542 / 548
页数:7
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