IP Library Granted Patent US 7,652,169
Granted Patent B2
US 7,652,169 · App. 12/227,519 · Granted Jan 26, 2010

(2R)-2-[(4-sulfonyl) aminophenyl] propanamides and pharmaceutical compositions containing them

Assignee: Dompe' Pha. R. Ma S.p.A.
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Quick Facts
Patent No.
US 7,652,169
App. No.
12/227,519
Granted
Jan 26, 2010
Kind
B2
Abstract

The present invention relates to novel (2R)-2-phenylpropanamides bearing a 4-sulfonylamino substituent on the 4 position of the phenyl group and to pharmaceutical compositions containing them, which are used as inhibitors of the chemotaxis of polymorphonucleate and mononucleate cells, and which are useful in the treatment of various ELR+CXC chemokine-mediated disorders. In particular, the compounds of the invention are useful in the treatment and control of specific CXCR2 dependent pathologies such as BOS, COPD, angiogenesis and melanoma.

Claims (49)

1. (2R)-2-phenylpropanamide derivatives of formula (I):

and pharmaceutically acceptable salts thereof,

wherein

R is selected from

H, OH, C 1 -C 5 -alkyl, C 3 -C 6 -cycloalkyl, C 2 -C 5 -alkenyl, C 1 -C 5 -alkoxy and phenyl;

an heteroaryl group selected from substituted and unsubstituted pyrrole, thiophene, furane, indole, imidazole, thiazole, oxazole, pyridine and pirimidine;

a residue of formula —CH 2 —CH 2 —O—(CH 2 —CH 2 O)nR″, wherein R″ is H or C 1 -C 5 -alkyl, n is an integer from 0 to 2;

or R, together with the NH group to which is coupled, is a radical group of primary amides of natural amino acids such as (2S)-2-aminopropanamide, (2S)-2-amino-3-phenylpropanamide, (2S)-2-amino-3-hydroxypropanamide, (2S)-2-amino-3-carboxypropanamide, (2S)-2,6-diaminoexanamide;

R′ is selected from

linear or branched C 1 -C 5 -alkyl, C 3 -C 6 -cycloalkyl, C 2 -C 5 -alkenyl and trifluoromethyl;

substituted or unsubstituted phenyl;

substituted or unsubstituted benzyl;

an heteroaryl group selected from substituted and unsubstituted pyridine, pirimidine, pyrrole, thiophene, furane, indole, thiazole and oxazole.

2. Compounds according to claim 1 wherein

R is selected from

H, C 1 -C 5 -alkyl, C 3 -C 6 -cycloalkyl, L-2-amino-1-methyl-2-oxoethyl;

an heteroaryl group selected from substituted and unsubstituted thiazole, oxazole, pyridine;

R′ is selected from

linear or branched C 1 -C 5 -alkyl, C 3 -C 6 -cycloalkyl, trifluoromethyl, benzyl;

unsubstituted or substituted phenyl with a group selected from halogen, C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, trifluoromethyl, thiophene.

3. Compounds according to claim 1 or 2 selected from:

(2R)-2-{4-[(isopropylsulfonyl]amino} phenyl)propanamide;

(2R)-2-{4-[(isopropylsulfonyl]amino } phenyl)propanamide sodium salt;

(2R)-2-{4-{[(2-chlorophenyl)sulfonyl]amino } phenyl) propanamide;

(2R)-2-{4-{[(2,6-dichlorophenyl)sulfonyl]amino } phenyl) propanamide;

(2R)-2-{4-[(methylsulfonyl)amino]phenyl } propanamide;

(2R)-2-{4-[(phenylsulfonyl)amino]phenyl}propanamide;

(2R)-2-{4-{[(4-methylphenyl)sulfonyl]amino } phenyl) propanamide;

(2R)-2-{4-{[(4-methoxylphenyl)sulfonyl]amino } phenyl) propanamide;

(2R)-2-(4-[(benzylsulfonyl]amino } phenyl)propanamide;

(2R)-2-(4-{[(4-chlorophenyl)sulfonyl]amino } phenyl)propanamide;

(2R)-2-(4-{[(4-(trifluoromethyl)phenyl]sulfonyl}amino)phenyl]propanamide;

(2R)-2-{4-[(thien-2ylsulfonyl)amino]phenyl } propanamide;

(2R)-2-{4-[(cyclopentylsulfonyl)amino]phenyl } propanamide;

(2R)-2-(4-{[(trifluoromethyl)sulfonyl]amino}phenyl) propanamide;

(2R)-2-{4-[(isopropylsulfonyl]amino } phenyl)-N-methylpropanamide;

(2R)-N-[( 1 S)-2-amino-1-methyl-2-oxoethyl]-2-(4-[(isopropylsulfonyl]amino } phenyl) propanamide;

(2R)-2-{4-[(isopropylsulfonyl]amino } phenyl)-N-[4-(trifluoromethyl)-1,3-thiazol-2-yl]propanamide;

(2R)-2-{4-{[(2-chlorophenyl)sulfonyl]amino } phenyl)-N-[4-(trifluoromethyl)-1,3-thiazol-2-yl]propanamide;

(2R)-2-{4-{[(2-chlorophenyl)sulfonyl]amino } phenyl)-N-[2-(2-hydroxyethoxy)ethyl]propanamide;

(2R)-2-{4-{[(2-chlorophenyl)sulfonyl]amino } phenyl)-N-cyclopropylpropanamide.

4. Compounds according to claim 3 which are:

(2R)-2-{4-[(isopropylsulfonyl]amino } phenyl)propanamide and its sodium salt.

5. A method for the treatment of diseases that involve CXCL1 induced human PMNs chemotaxis selected from the group consisting of chronic obstructive pulmonary disease (COPD) and obliterans syndrome (BOS) comprising administering to a subject in need thereof an effective amount of a compound of claim 1 .

6. Pharmaceutical compositions comprising a compound according to claim 1 in admixture with a suitable carrier thereof.

7. Process for the preparation of compounds of formula (I) according to claim 1 comprising the reaction of compound of formula (II),

wherein R′ has the same meaning as defined in claim 1 , with an amine of formula NHR,

wherein R has the same meaning as defined in claim 1 .

8. Process for the preparation of compounds of formula (I) according to claim 1 comprising the reaction of (2R)-2-(4-Aminophenyl)propanamide with a sulfonyl chlorides of formula R′ SO 2 Cl, wherein R′ has the same meaning as defined in claim 1 .

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY'S ADDRESS PREVIOUSLY RECORDED AT REEL: 036914 FRAME: 0863. ASSIGNOR(S) HEREBY CONFIRMS THE MERGER. Recorded Oct 6, 2016
From: DOMPÉ S.P.A.
To: DOMPÉ FARMACEUTICI S.P.A.
Reel/Frame 040246/0700 →
MERGER Recorded Oct 29, 2015
From: DOMPE' PHA.R.MA S.P.A.
To: DOMPÉ S.P.A.
Reel/Frame 036914/0385 →
MERGER Recorded Oct 29, 2015
From: DOMPÉ S.P.A.
To: DOMPÉ FARMACEUTICI S.P.A.
Reel/Frame 036914/0863 →
Priority Claims (1)
EP 06114185 · May 18, 2006 · regional
Continuity (1)
Related Publication 20090093530A1 · Apr 9, 2009