4-Chromenonyl-1,4-dihydropyridinecarbonitriles and the use thereof
View Patent ↗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.
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.