发明名称
摘要 PURPOSE:To prepare the title compound useful as a medicine having antiallergic effect, carcinostatic effect, antirheumatic effect, etc., easily, in high yield, by the ring-closing reaction of a pyridine derivative. CONSTITUTION:A compound of formula II (Y is O or S), e.g. 7-(1H-tetrazol-5- yl)-oxo-5H[1]benzopyrano[2,3-b]pyridine, is prepared by the ring-closing reaction of a compound of formula I (Py is pyridine ring; R<1>,<2> are H, halogen, lower alkyl, lower alkoxy, (substituted) phenyl, etc.; one of Y<1> and Y<2> is halogen, OH, mercapto, etc., and the other is OH, mercapto, lower alkyl, etc.; Z is acyl, carbamoyl, carboxyl, etc.), pref. in the presence of an acid such as HCl, a Friedel-Crafts catalyst such as AlCl3, and/or an alkali condensing agent such as NaH, at 20- 250 deg.C.
申请公布号 JPS638953(B2) 申请公布日期 1988.02.25
申请号 JP19790030623 申请日期 1979.03.15
申请人 YOSHITOMI PHARMACEUTICAL 发明人 OOE TAKANORI;TSURUTA MINEO
分类号 C07D495/04;A61K31/44;A61P37/08;C07D491/052 主分类号 C07D495/04
代理机构 代理人
主权项
地址