USRE38624EExpiredUtility
Hydroxyindoles, their use as inhibitors of phosphodiesterase 4 and process for their preparation
Est. expiryApr 28, 2018(expired)· nominal 20-yr term from priority
Inventors:Norbert HöfgenUte EgerlandHildegard KussDegenhard MarxStefan SzelenyiThomas KronbachEmmanuel PolymeropoulosSabine Heer
A61P 9/10A61P 9/00A61P 37/00A61P 9/08A61P 37/02A61P 7/12A61P 37/06A61P 43/00A61P 31/18A61P 33/06A61P 25/36A61P 25/28A61P 29/00A61P 25/16A61P 25/24A61P 3/10A61P 31/04A61P 25/02A61P 27/14A61P 25/00A61P 17/02A61P 13/12A61P 17/06A61P 13/08A61P 11/08A61P 19/00A61P 13/10A61P 19/08A61P 17/00A61P 1/04A61P 1/00A61P 11/00A61P 19/02A61P 11/06A61P 13/04A61P 17/04A61P 11/02A61P 21/00C07D 401/12C07D 209/22C07D 209/24
88
PatentIndex Score
20
Cited by
25
References
14
Claims
Abstract
The invention relates to new hydroxyindoles of the Formula, their use as inhibitors of phosphodiesterase 4 and processes for their preparation.
Claims
exact text as granted — not AI-modifiedWe claim:
1. A compound of the formula (I)
wherein
R 1 is a straight or branched C 1-3 C 1-12 alkyl optionally substituted with a phenyl radical, or
C 3-8 cycloalkyl residue radical wherein the phenyl residue radical is optionally substituted with a halo, nitro, hydroxy, C 1-4 alkyl, C 1-4 alkoxy, or COOH residue radical;
R 2 and R 3 are each independently of each other hydrogen, or an —OH residue radical where at least one of R 2 and R 3 are —OH;
R 5 is a pyridyl residue radical disubstituted with a halogen residue radical; and
A is a bond, C≡O, or a CHOH residue radical, or the pharmaceutically acceptable salt thereof.
2. The compound of claim 1 , wherein the compound is a pharmaceutically acceptable salt of an organic or inorganic acid, or of an organic or inorganic base, or a quaternary ammonium salt from the quaternization of a tertiary amine.
3. The compound of claim 1 , having an asymetric carbon atom by being the L or the D form, or a D,L mixture, and when in a diastereoisomeric form.
4. A compound of claim 1 , being one of the following compounds:
N-(3,5-dichloropyridin-4-yl)-2-[1-(4-fluorobenzyl)-5-hydroxyindol-3-yl]-2-oxoacetamide;
N-(3,5-dichloropyridin-4-yl)-2-[1-(4-fluorobenzyl)-5-hydroxyindol-3-yl]-2-oxoacetamide Na salt;
N-(3,5-dichloropyridin-4-yl)-2-[1-(4-fluorobenzyl)-5-hydroxyindol-3-yl]-2-hydroxyacetamide;
N-(pyridin-4-yl)-2-[1-2,6-difluorobenzyl)-5-hydroxyindol-3-yl]-2-oxyacetamide;
N-(3,5-dichloropyridin-4-yl)-2-[1-(2,6-difluorobenzyl)-5-hydroxyindol-3-yl]-2-oxoacetamide;
N-(3,5-dichloropyridin-4-yl)-2-[1-(3-nitrobenzyl)-5-hydroxyindol-3-yl]-2-oxoacetamide Na salt;
N-(3,5-dichloropyridin-4-yl)-2-(1-propyl-5-hydroxyindol-3-yl)-2-oxyacetamide;
N-(3,5-dichloropyridin-4-yl)-2-(1-isopropyl-5-hydroxyindol-3-yl)-2-oxoacetamide;
N-(3,5-dichloropyridin-4-yl)-2-(1-cyclopentylmethyl-5-hydroxyindol-3-yl)-2-oxoacetamide;
N-(2,6-dichlorophenyl)-2-[1-(4-fluorobenzyl)-5-hydroxyindol-3-yl]-2-oxoacetamide;
N-(2,6-dichloro-4-trifluoromethylphenyl)-2-[1-(4-fluorobenzyl)-5-hydroxyindol-3-yl)-2-oxoacetamide;
N-(2,6-dichloro-4-trifluoromethoxylphenyl)-2-[1-(4-fluorobenzyl)-5-hydroxyindol-3-yl)-2-oxoacetamide;
N-(3,5-dichloropyridin-4-yl)-2-[1-(4-fluorobenzyl)-6-hydroxyindol-3-yl]-2-oxoacetamide;
N-(3,5-dichloropyridin-4-yl)-5-hydroxy-1-(4-methoxybenzyl)indole-3-carboxamide.
5. A process for inhibiting TNFα by administering to a patient in need therefor an effective amount of the compound of claim 1 .
6. A process for inhibiting TNFα by administering to a patient in need therefor an effective amount of the compound of claim 4 2 .
7. A process for inhibiting phosphodiesterase 4 by administering to a patient in need therefor an effective amount of the compound of claim 1 .
8. A process for inhibiting phosphodiesterase 4 by administering to a patient in need therefor an effective amount of the compound of claim 4 2 .
9. A process for treating an eosinophil-related condition by administering to a patient in need therefor an effective amount of the compound of claim 1 .
10. A process for treating an eosinophil-related condition by administering to a patient in need therefor an effective amount of the compound of claim 4 2 .
11. A process for treating a chronic obstructive pulmonary disease, which comprises administering to a patient in need therefor an effective amount of a compound of claim 1 .
12. A process for treating a chronic obstructive pulmonary disease, which comprises administering to a patient in need therefor an effective amount of a compound of claim 4 2 .
13. A pharmaceutical preparation which comprises a therapeutically effective amount of the compound of claim 1 , together with one or more of a pharmaceutically acceptable carrier, diluent, and auxiliary ingredient.
14. A process for preparing the pharmaceutical preparation of claim 7 , which comprises preparing a pharmaceutically acceptable dosage form from a compound of formula (I)and from one or more of a pharmaceutically acceptable carrier, diluent, and auxiliary ingredient.Cited by (0)
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