IP Library Granted Patent US 8,263,621
Granted Patent B2
US 8,263,621 · App. 12/400,187 · Granted Sep 11, 2012

Tartrate derivatives for use as coagulation factor IXa inhibitors

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,263,621
App. No.
12/400,187
Granted
Sep 11, 2012
Kind
B2
Abstract

The invention relates to the compounds of formula I having antithrombotic activity which especially inhibits blood clotting factor IXa, to methods for producing the same and to the use thereof as drugs.

Claims (29)

1. A compound of formula I

or a stereoisomeric form of a compound of formula I, or a mixture of such forms in any ratio, or a physiologically tolerable salt of a compound of formula I

where

R1 is carbamimidoylphenyl, aminomethylphenyl or Het-Z, where Het is selected from the group consisting of benzimidazolyl and isoquinolinyl, and in which Z is amino or amidino,

R2 and R4 are in each case a hydrogen atom,

R3 is

1) phenyl, in which phenyl is unsubstituted or mono- or disubstituted by T,

2)-phenyl-Q-phenyl, in which the two phenyl radicals in each case independently of one another are unsubstituted or mono- or disubstituted by T or

3) phenyl-Q-Het-2, in which Het-2 is selected from the group consisting of quinolinyl, quinoxalinyl, furanyl, indolyl, isoquinolinyl, isothiazolyl, isoxazolyl, oxadiazolyl, piperidinyl, pyrazolyl, pyridazinyl, pyrimidinyl, pyridyl, pyrimidinyl, pyrrolyl, thiadiazolyl, thiazolyl, thienyl, thienopyrrolyl or thienothiophenyl, and in which phenyl and Het-2 in each case independently of one another are unsubstituted or mono- or disubstituted by T,

Q is a covalent bond, —CH 2 —, —N(CH 3 )— or —O—,

T is

1) F, Cl or Br,

2) —(C 1 -C 4 )-alkyl, in which alkyl are unsubstituted or independently mono- or disubstituted by —CF 3 or —N—C(O)—CH 3 , or

3) —NO 2 , and

R5 and R6 are in each case a hydrogen atom.

2. A compound of formula I as claimed in claim 1 which is the compound

(2R,3R)—N-(1-aminoisoquinolin-6-yl)-2,3-dihydroxy-N′-p-tolylsuccinamide,

(2R,3R)—N-(2-amino-3H-benzimidazol-5-yl)-2,3-dihydroxy-N′-p-tolyl-succinamide,

(2R,3R)—N-(2-amino-3H-benzimidazol-5-yl)-N-(4-cyclohexylphenyl)-2,3-dihydroxysuccinamide,

(2R,3R)—N-(4-aminomethylphenyl)-2,3-dihydroxy-N′-p-tolylsuccinamide,

(2R,3R)—N-(4-carbamimidoylphenyl)-2,3-dihydroxy-N′-p-tolylsuccinamide,

(2R,3R)—N-(2-amino-3H-benzimidazol-5-yl)-N′-(4-fluorophenyl)-2,3-dihydroxysuccinamide,

(2R,3R)—N-(2-amino-3H-benzimidazol-5-yl)-N-(4-chlorophenyl)-2,3-dihydroxysuccinamide,

(2R,3R)—N-(2-amino-3H-benzimidazol-5-yl)-2,3-dihydroxy-N′-phenyl-succinamide,

(2R,3R)—N-(2-amino-3H-benzimidazol-5-yl)-2,3-dihydroxy-N′-(4-nitrophenyl)-succinamide,

(2R,3R)—N-(2-amino-3H-benzimidazol-5-yl)-2,3-dihydroxy-N′-(4-isopropyl-phenyl)succinamide,

(2R,3R)—N-(2-amino-3H-benzimidazol-5-yl)-2,3-dihydroxy-N′-(4-piperidin-1-yl-phenyl)succinamide or

(2R,3R)—N-(2-amino-3H-benzimidazol-5-yl)-2,3-dihydroxy-N-(4-phenoxy-phenyl)succinamide.

3. A medicament comprising an efficacious amount of at least one compound of formula I as claimed in claim 1 together with a pharmaceutically suitable and physiologically tolerable vehicle, additive or other active substances and auxiliaries.

Assignments (2)
CHANGE OF NAME Recorded Jun 20, 2012
From: SANOFI-AVENTIS
To: SANOFI
Reel/Frame 028413/0927 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 17, 2009
From: STEINHAGEN, HENNING; FOLLMANN, MARKUS; GOERLITZER, JOCHEN; SCHREUDER, HERMAN
To: SANOFI-AVENTIS
Reel/Frame 023243/0227 →