发明名称 PHENYL-AND AMINOPHENYL-ALKYLSULFONAMIDE AND UREA DERIVATIVE
摘要 PROBLEM TO BE SOLVED: To obtain a new compound useful as anα1 A/1 L-adrenaline receptor agonist. SOLUTION: This new compound is shown by formula I [A is R<1> q (R<3> R<60> N)m (Z)(NR<2> )n ; (m) and (q) are each 0 or 1; Z is C=O or SO2 ; (n) is 1; X is NH, CH2 or OCH2 ; Y is 2-imidazoline, 2-oxazoline, 2-thiazoline or 4-imidazole; R<1> to R<3> and R<60> are each H, a lower alkyl, phenyl or the like; R<4> to R<7> are each H, a lower alkyl, CF3 , a lower alkoxy, halogen, phenyl, a lower alkenyl, hydroxyl, a lower alkylsulfonamido or the like], e.g. N-[(3-(4,5-dihydro-1H-imidazol-2- ylmethoxy)phenyl]methanesulfonamide. The compound of' formula I is obtained by reaction of a compound of formula II with 1,2-diaminoethane (in the case that A is R<1> SO2 NH, X is CH2 or OCH2 , Y is 2-imidazoline). This new compound is effective for such diseases as incontinence of urine, nasal congestion, priapism, depression, anxiety, dementia and senility.
申请公布号 JPH1171353(A) 申请公布日期 1999.03.16
申请号 JP19980172403 申请日期 1998.06.19
申请人 F HOFFMANN LA ROCHE AG 发明人 COURNOYER RICHARD LEO;KEITZ PAUL FRANCIS;O'YANG COUNDE;YASUDA DENNIS MITSUGU
分类号 C07D233/20;A61K31/00;A61K31/415;A61K31/4174;A61K31/4178;A61K31/42;A61K31/421;A61K31/425;A61P3/00;A61P3/04;A61P13/00;A61P13/02;A61P15/00;A61P25/00;A61P25/20;A61P25/24;A61P25/26;A61P25/28;A61P27/00;A61P27/16;A61P43/00;C07D;C07D209/08;C07D233/08;C07D233/22;C07D233/24;C07D233/50;C07D233/54;C07D233/64;C07D233/66;C07D263/28;C07D263/38;C07D263/64;C07D277/10;C07D277/18;C07D277/28;C07D277/34;C07D277/38;C07D403/06;C07D403/10;C07D403/12;C07D413/06;C07D413/12;(IPC1-7):C07D233/22 主分类号 C07D233/20
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