Shestopalov Anatoliy M, Larionova Natalia A, Fedorov Alexander E, Rodinovskaya Lyudmila A, Mortikov Valery Yu, Zubarev Andrey A, Bushmarinov Ivan S
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences , 119991 Moscow, Russian Federation.
ACS Comb Sci. 2013 Oct 14;15(10):541-5. doi: 10.1021/co400066y. Epub 2013 Sep 4.
Isothiazolothienopyridines have been prepared by a domino reaction (the SN2 reaction → the Thorpe-Ziegler reaction → the Thorpe-Guareschi reaction type) from disodium 4-cyanoisothiazole-3,5-dithiolate. By changing the order of addition of the alkylation reagents in the reaction with disodium 4-cyanoisothiazole-3,5-dithiolate both possible isomers of the isothiazolothienopyridines are synthesized. These isomers were further used in three-component domino reaction (the Knoevenagel reaction → the Michael reaction → the hetero-Thorpe-Ziegler reaction type) to obtain wide range of isomeric isothiazolothienopyranopyridines.
异噻唑并噻吩并吡啶是由4-氰基异噻唑-3,5-二硫醇二钠通过多米诺反应(SN2反应→索普-齐格勒反应→索普-瓜雷斯基反应类型)制备而成。通过改变与4-氰基异噻唑-3,5-二硫醇二钠反应时烷基化试剂的添加顺序,可以合成异噻唑并噻吩并吡啶的两种可能异构体。这些异构体进一步用于三组分多米诺反应(克诺文纳盖尔反应→迈克尔反应→杂环索普-齐格勒反应类型),以获得多种异构的异噻唑并噻吩并吡喃并吡啶。