IP Library Granted Patent US 8,058,447
Granted Patent B2
US 8,058,447 · App. 11/989,279 · Granted Nov 15, 2011

4-Chromenonyl-1,4-dihydropyridinecarbonitriles and the use thereof

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Quick Facts
Patent No.
US 8,058,447
App. No.
11/989,279
Granted
Nov 15, 2011
Kind
B2
Abstract

The present application relates to novel 4-chromenonyl-1,4-dihydropyridinecarbonitriles, processes for their preparation, pharmaceutical compositions containing them, and their use for the treatment and/or prophylaxis of diseases, especially cardiovascular disorders.

Claims (57)

1. A compound of the formula (I)

in which

R 1 and R 2 are identical or different and are independently of one another (C 1 -C 4 )-alkyl, trifluoromethyl, cyclopropyl or cyclobutyl,

A is a bond or O,

R 3 is (C 3 -C 7 )-cycloalkyl or is (C 1 -C 6 )-alkyl which may be substituted by (C 3 -C 7 )-cycloalkyl or once to three times by fluorine,

R 4 is hydrogen, halogen, cyano, nitro, trifluoromethyl, (C 1 -C 4 )-alkyl or (C 1 -C 4 )-alkoxy

and

R 5 is hydrogen or fluorine,

or a salt thereof.

2. The compound of the formula (I) as claimed in claim 1 , in which

R 1 and R 2 are identical or different and are methyl or trifluoromethyl,

A is a bond or is O,

R 3 is (C 3 -C 5 )-cycloalkyl or is (C 1 -C 6 )-alkyl which may be substituted by (C 3 -C 5 )-cycloalkyl or once to three times by fluorine,

R 4 is hydrogen, fluorine, chlorine, cyano, nitro or methyl

and

R 5 is hydrogen or fluorine,

or a salt thereof.

3. The compound of the formula (I) as claimed in claim 1 , in which

R 1 is methyl or trifluoromethyl,

R 2 is methyl,

A is O,

R 3 is ethyl, 2,2,2-trifluoroethyl, n-propyl, isopropyl, 1-(trifluoromethyl)ethyl, tertbutyl, cyclobutyl, cyclopentyl, cyclopropylmethyl or cyclobutylmethyl,

R 4 is hydrogen, fluorine, chlorine or nitro

and

R 5 is hydrogen or fluorine,

or a salt thereof.

4. The compound of the formula (I) as claimed in claim 1 , in which

R 1 is methyl or trifluoromethyl,

R 2 is methyl,

A is a bond,

R 3 is isobutyl, isopentyl, cyclobutylmethyl, cyclopentylmethyl, 2-(cyclopropyl)ethyl, 2-(cyclobutyl)ethyl or 2-(cyclopentyl)ethyl,

R 4 is hydrogen, fluorine, chlorine or nitro

and

R 5 is hydrogen or fluorine,

or a salt thereof.

5. A process for preparing compounds of the formula (I) as defined in claim 1 , characterized in that a compound of the formula (II)

in which R 4 and R 5 each have the meanings indicated in claim 1 ,

either

[A] is reacted in a one-stage process (one-pot reaction) with a compound of the formula (III)

in which R 1 has the meanings indicated in claim 1 ,

and a compound of the formula (IV)

in which A, R 2 and R 3 each have the meanings indicated in claim 1

or

[B] is reacted in a one-stage process (one-pot reaction) with a compound of the formula (V)

in which R 1 has the meanings indicated in claim 1 ,

and a compound of the formula (VI)

in which A, R 2 and R 3 each have the meanings indicated in claim 1

or

[C] is converted in a two-stage process firstly with a compound of the formula (III) into compounds of the formula (VII)

in which R 1 , R 4 and R 5 each have the meanings indicated in claim 1 ,

and the latter is then reacted in a second step with a compound of the formula (IV)

or

[D] is converted in a two-stage process firstly with a compound of the formula (VI) into compounds of the formula (VIII)

in which A, R 2 , R 3 , R 4 and R 5 each have the meanings indicated in claim 1 ,

and the latter is then reacted in a second step with a compound of the formula (V).

6. A pharmaceutical composition comprising a compound of the formula (I) as defined in claim 1 in combination with an inert, non-toxic, pharmaceutically suitable excipient.

7. A pharmaceutical composition comprising a compound of the formula (I) as defined in claim 1 in combination with a further active ingredient selected from the group consisting of ACE inhibitors, renin inhibitors, angiotensin II receptor antagonists, beta blockers, acetylsalicylic acid, diuretics, potassium supplements, calcium antagonists, statins, digitalis (digoxin) derivatives, calcium sensitizers, nitrates, anticoagulants, antiarrhythmics, vasodilators, and thrombolytics.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 1, 2013
From: BAYER PHARMA AKTIENGESELLSCHAFT
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 029904/0996 →
CHANGE OF NAME Recorded Oct 3, 2011
From: BAYER SCHERING PHARMA AG
To: BAYER PHARMA AKTIENGESELLSCHAFT
Reel/Frame 027009/0182 →
MERGER Recorded Feb 18, 2011
From: BAYER HEALTHCARE AG
To: BAYER SCHERING PHARMA AKTIENGESELLSCHAFT
Reel/Frame 025837/0666 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 16, 2009
From: KUHL, ALEXANDER; KOLKHOF, PETER; HECKROTH, HEIKE; SCHLEMMER, KARL-HEINZ; FLAMME, INGO; FIGUEROA PEREZ, SANTIAGO; GIELEN-HAERTWIG, HEIKE; GROSSER, ROLF; ERGUDEN, JENS-KERIM; LANG, DIETER
To: BAYER HEALTHCARE AG
Reel/Frame 022397/0146 →