Synthesis of thiazolo[5,4-d]pyrimidine, thiazolo[5,4-b]pyridine, thiazolo[4,5-b]pyrrolizine and thiazolo[5,4-d]thiazaphosphinine

被引:4
作者
El-Emary, T. I.
Khodairy, A.
机构
[1] Assiut Univ, Dept Chem, Assiut 71516, Egypt
[2] S Valley Univ, Dept Chem, Sohag, Egypt
关键词
5-amino-2-methylsulfanyl-thiaozle-4-carboxylic acid ethyl ester; thiazolopyridine; thiazolopyrimidines; thiazolothiazaphosphinine;
D O I
10.1080/10426500500326362
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
5-amino-2-methylsulfanyl-thiazole-4-carboxylic acid ethyl ester 1 reacted with malononitrile, benzoylisothiocyanate, and 2-(methylsulfanyl-phenylaminomethylene)malononitrile to furnish the thiazolopyrimidine-2-one derivatives 2- 4, respectively. 1 reacted with the dipotassium salt of the 2-dimercaptomethylene-malononitrile prepared by the reaction of malononitrile and CS2 and KOH in the presence of TBAB under solid-liquid phase transfer catalysis to give 5. Reacting 1 with triethyl orthoformate, chloroacetyl chloride, and 2,5 dimethoxy tetrahydrofuran afforded 6-8. The reaction of 1 with Lawesson's reagent gave 9. The reaction of 1 with benzylidinemalononitrile gave 10. The reaction of hydrazine hydrate with 1 and/or 6 afforded 11 and 12, respectively. 7 reacted with malononitrile to give 13. The cyclization of 8 by the action of PPA gave 14. Thiazole-4-carbohydrazide 11 reacted with acetic anhydride/acetic acid mixture and with formic acid to yield 15 and 16, respectively. 11 reacted with p-chloro benzaldehyde to give 17. The treatment of compound 17 and/or 11 with triethyl orthoformate afforded 18 and 19, respectively. The reaction of 11 with CS2 and with 2-(bismethylsulfanyl-methylene) malononitrile gave 20 and 21, respectively.
引用
收藏
页码:1073 / 1085
页数:13
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