发明名称 2,6-SUBSTITUTED 3-££2'-(1H-TETRAZOL-5-YL)£1,1'-BIPEHNYL|-4- -YL|METHYL-4(3H)-QUINAZOLINE COMPOUND, METHOD AND INTERMEDIATE PRODUCTS FOR ITS PREPARATION AND PHARMACEUTICAL COMPOSITION ON ITS BASE
摘要 <p>This patent deals with a solution related to 2,6- -substituted 3-[[2'-(1H-tetrazol-5-yl)[1,1'-bipehnyl]-4- -yl]methyl-4(3H)-quinazoline compound with general formula (I), where X is direct or branched alkyl, n is 1 up to 3, R6 is a group with a formula (i), (ii), (iii), (iv), (v), (vi), (vii) or (viii), where R9 is H, alkyl with a direct chain phenyl, mono substituted phenyl, where a substituent is selected of the group including alkyl, -CF3, nitro, O-alkyl or -NH2, and also pyridine or thiophene or furan, R10 is H, alkyl with a direct chain, phenyl monosubstituted phenyl, where the substituent is selected of the group which includes alkyl, -CF3, nitro, O-alkyl or -NH2 and pyridine, thiophene or furan, however there is a condition that R9 and R10 cannot mean hydrogen simultaneously, R11 is H, alkyl R12 with a direct chain, phenyl monosubstisturted phenyl, where the substituent is selected of the group containing alkyl, -CF3, nitro, O-alkyl or -NH2 and pyridine, thiophene or furane, R17 is alkyl or salts acceptable form pharmaceutical point of view, while this patent describes intermediate products for preparation of this compound prepared based on this compound. The compound with a general formula (I) has a higher efficiency of antagonists of angiothesine II.</p>
申请公布号 SK279004(B6) 申请公布日期 1998.05.06
申请号 SK19920000255 申请日期 1992.01.29
申请人 VENKATESAN ARANAPAKAM M.;JEREMY LEVIN I. 发明人 VENKATESAN ARANAPAKAM M.;JEREMY LEVIN I.
分类号 A61K31/505;A61K31/517;A61P9/00;A61P9/12;A61P43/00;C07D239/88;C07D239/90;C07D239/91;C07D257/04;C07D403/10;C07F7/08;C07F7/18;(IPC1-7):C07D403/10;A61K31/455 主分类号 A61K31/505
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