发明名称 2,4-BIS[(4-AMIDINO)PHENYL]FURAN AS ANTI-PNEUMOCYSTIS CARINI PNEUMONIC AGENT
摘要 PROBLEM TO BE SOLVED: To obtain the subject new compound capable of expressing useful antimicrobial activity through strongly binding to a DNA, therefore useful for treating Pneumocystis carini pneumonia. SOLUTION: This new compound is a compound of formula I (R1 and R2 are each H, a lower alkyl, aryl, alkylaryl, aminoalkyl, aminoaryl, a halogen, or the like; R3 and R4 are each H, a lower alkyl, oxyalkyl, alkylaryl, aryl, or the like; X and Y are each located at a p- or m-site, being H, a lower alkyl, oxyalkyl, or the like), e.g. 2,4-bis 4-[(amidino)phenyl]}furan. The compound of formula I is synthesized, for example, by reacting a compound of formula II in the presence of a base to form a compound of formula III (X is a halogen, pref. Br or I), which is then reacted with CuCN in the presence of DMF to form 2,4-bis(4-cyanophenyl)furan as its important intermediate. It is prefarable to use the compound of formula I at a dose of 0.1-50 m/kg.
申请公布号 JP2000256343(A) 申请公布日期 2000.09.19
申请号 JP19980217593 申请日期 1998.07.31
申请人 UNIV NORTH CAROLINA AT CHAPEL HILL:THE 发明人 BOYKIN DAVID W;TIDWELL RICHARD R;WILSON W DAVID;FRANCESCONI IRIS
分类号 A61K31/34;A61K31/341;A61P11/00;A61P29/00;A61P33/02;C07D307/52;C07D307/54;C07D405/10;C07D405/14;(IPC1-7):C07D307/54 主分类号 A61K31/34
代理机构 代理人
主权项
地址