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:
Nov. 16, 1999

Filed:

Jul. 15, 1997
Applicant:
Inventors:

Hidenori Ogawa, Tokushima-ken, JP;

Hisashi Miyamoto, Kyoto-fu, JP;

Kazumi Kondo, Tokushima-ken, JP;

Hiroshi Yamashita, Tokushima-ken, JP;

Kenji Nakaya, Tokushima-ken, JP;

Hajime Komatsu, Tokushima-ken, JP;

Michinori Tanaka, Tokushima-ken, JP;

Shinya Kora, Nagasaki-ken, JP;

Michiaki Tominaga, Tokushima-ken, JP;

Yoichi Yabuuchi, Tokushima-ken, JP;

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
A61K / ; A61K / ; A61K / ; C07D / ; C07D / ; C07D / ; C07D / ; C07D / ;
U.S. Cl.
CPC ...
514221 ; 514183 ; 514220 ; 5142282 ; 5142285 ; 5142328 ; 5142345 ; 514248 ; 514249 ; 514250 ; 514259 ; 514267 ; 540461 ; 540471 ; 540473 ; 540495 ; 540510 ; 540517 ; 540557 ; 540567 ; 540569 ; 540573 ; 544 60 ; 544 62 ; 544115 ; 544116 ; 544234 ; 544235 ; 544237 ; 544250 ; 544251 ; 544283 ; 544345 ; 544353 ;
Abstract

Novel benzoheterocyclic compounds of the formula: ##STR1## wherein R.sup.1 is H, halogen, alkyl, optionally substituted amino, alkoxy; R.sup.2 is H, halogen, alkoxy, phenylalkoxy, OH, alkyl, optionally substituted amino, carbamoyl-alkoxy, optionally substituted amino-alkoxy, optionally substituted benzoyloxy; R.sup.3 is a group: --NR.sup.4 R.sup.5 or --CO--NR.sup.11 R.sup.12 ; R.sup.4 is H, optionally substitued benzoyl, alkyl; R.sup.5 is a group: ##STR2## [R.sup.16 is halogen, optionally substituted alkyl, OH, alkoxy, alkanoyloxy, alkylthio, alkanoyl, carboxy, alkoxycarbonyl, CN, NO.sub.2, optionally substituted amino, phenyl, cycloalkyl, etc., or a group: --O--A--NR.sup.6 R.sup.7 ; m is 0 to 3], phenyl-alkoxycarbonyl, alkanoyl, phenylalkanoyl, etc.; R.sup.11 is H or alkyl; R.sup.12 is cycloalkyl or optionally substituted phenyl; and W is a group: --(CH.sub.2).sub.p (p is 3 to 5) or --CH.dbd.CH--(CH.sub.2).sub.q (q is 1 to 3), the carbon atom of these groups beign optionally replaced by O, S, SO, SO.sub.2 or a group: --N(R.sup.13)-- and further these groups having optionally 1 to 3 substituents of alkyl, alkoxycarbonyl, carboxy, OH, O, alkanoyloxy, etc., which have excellent vasopressin antagonistic activities and are useful as vasodilator, hypotensive agent, water diuretics, platelet agglutination inhibitor, and a vasopressin antagonistic composition containing the compound as the active ingredient.


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