The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jan. 17, 1989

Filed:

Apr. 14, 1986
Applicant:
Inventors:

Sheung T Kam, Chicago, IL (US);

William L Matier, Libertyville, IL (US);

Ghanshyam Patil, Vernon Hills, IL (US);

Khuong H Mai, Waukegan, IL (US);

Assignee:
Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C07D / ; C07D / ;
U.S. Cl.
CPC ...
544146 ; 544 584 ; 544 585 ; 544 587 ; 544137 ; 544139 ; 544143 ; 544152 ; 544369 ; 544370 ; 544373 ; 544376 ; 544379 ; 546196 ; 546201 ; 546202 ; 546209 ; 546212 ; 546214 ; 548225 ; 548236 ; 548336 ; 548337 ; 548339 ; 548343 ; 548455 ; 548467 ; 548492 ; 548517 ; 548518 ; 548525 ; 548527 ; 549 57 ; 549 59 ; 549 60 ; 549 61 ; 549 64 ; 549 68 ; 549 69 ; 549 71 ; 549467 ; 549473 ; 549474 ; 549479 ; 549481 ; 549484 ; 549486 ;
Abstract

The present invention relates to compounds of the general formula ##STR1## wherein Ar represents a substituted or unsubstituted heterocyclic group; W represents alkylene of from 1 to about 10 carbon atoms; and B represents --NR.sub.2 COR.sub.1, --NR.sub.2 CONR.sub.1 R.sub.3, --NR.sub.2 SO.sub.2 R.sub.1, NR.sub.2 SO.sub.2 NR.sub.1 R.sub.3, or --NR.sub.2 COOR.sub.1, wherein R.sub.1, R.sub.2 and R.sub.3 may be alike or different and may be hydrogen, alkyl, alkoxyalkyl cycloalkyl, alkenyl, alkynyl, aryl, heteroaryl, or aralkyl, except that R.sub.1 is not hydrogen when B is --NR.sub.2 SO.sub.2 R.sub.1 or --NR.sub.2 COOR.sub.1, or R.sub.1 and R.sub.3 may together with N form a 5 to 7 membered heterocyclic group and the pharmaceutically acceptable salts thereof. The compounds exhibit beta-adrenergic blocking activity and are also useful in the treatment of glaucoma.


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