作者:Emmanuel A. Adegoke、Babajide I. Alo、Oluwole B. Familoni
DOI:10.1002/jhet.5570240122
日期:1987.1
Regiospecific synthesis of 4H-3,3a-dihydrothiazolo[4,3-b]quinazolines and 7-methyl-4H-3,3a-dihydrothiazolo[4,3-b]quinazolines IVa and IVb is described. The N-substituted thiazolidinecarboxylic acids Ia and Ib were converted to the corresponding acid chlorides, IIa and IIb but neither reacted with silver trifluoromethanesulphonate. The carboxylic acids Ic and Id were however, decarboxylated to the corresponding
描述了4 H -3,3a-二氢
噻唑并[4,3- b ]
喹唑啉和7-甲基-4 H -3,3a-二氢
噻唑并[4,3- b ]
喹唑啉IVa和IVb的区域特异性合成。所述Ñ取代
噻唑烷酸IA和磅被转化为相应的酰基
氯,IIA和IIB但既不与
三氟甲磺酸银反应。但是,使用三
氯氧化
磷将
羧酸Ic和Id脱羧成相应的
亚胺离子,得到了
硝胺IIIa和IIIb。还原环化产生
喹唑啉IVa和IVb。