A novel and expeditious route to A-81988: An angiotensin II receptor antagonist

被引:5
作者
Kerdesky, FAJ
Sowin, TJ
机构
[1] Process Research, Pharmaceutical Products Division, Abbott Laboratories, North Chicago
关键词
D O I
10.1080/00397919608003705
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A novel and efficient synthesis of A-81988, an angiotensin II receptor antagonist, is described. The key step utilizes a palladium-catalyzed biaryl coupling between a phenylboronic acid derivative and N-trityl-5-(2-bromophenyl)tetrazole.
引用
收藏
页码:1007 / 1013
页数:7
相关论文
共 7 条
[1]   DISCOVERY OF A NOVEL CLASS OF ORALLY ACTIVE, NONPEPTIDE ANGIOTENSIN-II ANTAGONISTS [J].
DE, B ;
WINN, M ;
ZYDOWSKY, TM ;
KERKMAN, DJ ;
DEBERNARDIS, JF ;
LEE, J ;
BUCKNER, S ;
WARNER, R ;
BRUNE, M ;
HANCOCK, A ;
OPGENORTH, T ;
MARSH, K .
JOURNAL OF MEDICINAL CHEMISTRY, 1992, 35 (20) :3714-3717
[2]   THE DISCOVERY OF DUP-753, A POTENT, ORALLY ACTIVE NONPEPTIDE ANGIOTENSIN-II RECEPTOR ANTAGONIST [J].
DUNCIA, JV ;
CARINI, DJ ;
CHIU, AT ;
JOHNSON, AL ;
PRICE, WA ;
WONG, PC ;
WEXLER, RR ;
TIMMERMANS, PBMWM .
MEDICINAL RESEARCH REVIEWS, 1992, 12 (02) :149-191
[3]   AN EFFICIENT SYNTHESIS OF AN ANGIOTENSIN-II ANTAGONIST (A-81988) [J].
KERDESKY, FAJ ;
HAIGHT, A ;
NARAYANAN, BA ;
NORDEEN, CW ;
SCARPETTI, D ;
SEIF, LS ;
WITTENBERGER, S ;
MORTON, HE .
SYNTHETIC COMMUNICATIONS, 1993, 23 (14) :2027-2039
[4]   THE PALLADIUM-CATALYZED CROSS-COUPLING REACTION OF PHENYLBORONIC ACID WITH HALOARENES IN THE PRESENCE OF BASES [J].
MIYAURA, N ;
YANAGI, T ;
SUZUKI, A .
SYNTHETIC COMMUNICATIONS, 1981, 11 (07) :513-519
[5]  
Shuman R. F., 1991, [No title captured], Patent No. [US 5039814, 5039814]
[6]   SYNTHESIS OF AROMATIC BORONIC ACIDS - ALDEHYDO BORONIC ACIDS AND A BORONIC ACID ANALOG OF TYROSINE [J].
SNYDER, HR ;
REEDY, AJ ;
LENNARZ, WJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1958, 80 (04) :835-838
[7]  
TASKER AS, 1993, 206TH ACS NAT M CHIC