-
公开(公告)号:US4329468A
公开(公告)日:1982-05-11
申请号:US162353
申请日:1980-06-24
IPC分类号: C07D215/22 , C07D215/227 , C07D215/26
CPC分类号: C07D215/227 , C07D215/26
摘要: Novel compounds represented by the formula ##STR1## wherein R.sup.1, R.sup.2, R' and R" are defined as hereinafter, having a blocking activity on .beta.-adrenergic nerves, novel intermediates useful for synthesis thereof and processes for preparing the same are disclosed. When substitution is at the 5-position and R.sup.1 and R.sup.2 are hydrogen, R' and R" are not simultaneously hydrogen and a 1 to 4 carbon atom alkyl group in the claimed compound.
摘要翻译: 由式(I)表示的新型化合物,其中R1,R2,R'和R“定义如下,对β-肾上腺素能神经具有阻断活性,可用于其合成的新中间体及其制备方法 被披露。 当取代为5位且R 1和R 2为氢时,R'和R“不是所要求保护的化合物中的氢和1至4个碳原子的烷基。
-
2.
公开(公告)号:US4256890A
公开(公告)日:1981-03-17
申请号:US886373
申请日:1978-03-14
IPC分类号: C07D215/22 , C07D215/227 , C07D215/26
CPC分类号: C07D215/227 , C07D215/26
摘要: Novel compounds represented by the formula ##STR1## wherein R.sup.1, R.sup.2, and R' and R" are defined as hereinafter, having a blocking activity on .beta.-adrenergic nerves, novel intermediates useful for synthesis thereof and processes for preparing the same are disclosed. When substitution is at the 5-position and R.sup.1 and R.sup.2 are hydrogen, R' and R" are not simultaneously hydrogen and a 1 to 4 carbon atom alkyl group in the claimed compound.
摘要翻译: 由式(I)表示的新型化合物,其中R1,R2和R'和R“定义如下,对β-肾上腺素能神经具有阻断活性,可用于其合成的新中间体和制备 同样披露。 当取代为5位且R 1和R 2为氢时,R'和R“不是所要求保护的化合物中的氢和1至4个碳原子的烷基。
-
公开(公告)号:US3953456A
公开(公告)日:1976-04-27
申请号:US424965
申请日:1973-12-14
IPC分类号: C07D215/22 , A61K31/47 , A61P9/06 , A61P9/08 , A61P9/10 , C07D215/227 , C07D215/26
CPC分类号: C07D215/227 , C07D215/26
摘要: 2-Hydroxy-3-alkylaminopropoxycarbostyrils represented by the formula (I) ##SPC1##wherein R represents a straight or branched chain alkyl group having 1 to 4 carbon atoms useful as .beta.-adrenergic blocking agents and a process for preparing the same are disclosed.
摘要翻译: 公开了式(I)所示的2-羟基-3-烷基氨基丙氧基卡波斯特利,其中R表示可用作β-肾上腺素能阻断剂的具有1至4个碳原子的直链或支链烷基及其制备方法。
-
4.
公开(公告)号:US4065456A
公开(公告)日:1977-12-27
申请号:US517730
申请日:1974-10-24
申请人: Kazuyuki Nakagawa , Nanami Murakami , Hideo Mori , Kaoru Tanimura
发明人: Kazuyuki Nakagawa , Nanami Murakami , Hideo Mori , Kaoru Tanimura
IPC分类号: C07C45/71 , C07C49/755 , C07D215/20 , C07D215/22 , C07D215/227 , C07D215/26 , C07D217/24 , C07D319/18
CPC分类号: C07D215/227 , C07C45/71 , C07C49/755 , C07D215/20 , C07D215/26 , C07D217/24 , C07D319/18 , Y10S514/822
摘要: A glycerol derivative represented by the formula (I) ##STR1## wherein A is hereinafter defined, including the optically active isomers per se and mixtures of the optically active isomers, which are useful as a central nervous system depressant, an intermediate for the preparation of .beta.-adrenergic blocking agents, an inhibitor of blood platelet aggregation or a choleretic agent, and a process for preparing the above glycerol derivative.
摘要翻译: 由下式定义的式(I)表示的甘油衍生物,其中A定义如下,包括光学活性异构体本身以及可用作中枢神经系统抑制剂的光学活性异构体的混合物, β-肾上腺素能阻断剂的制备,血小板聚集抑制剂或胆固醇剂,以及制备上述甘油衍生物的方法。
-
-
-