IP Library › Granted Patent US 7,629,337

Granted Patent B2

US 7,629,337 · App. 11/494,943 · Granted Dec 8, 2009

Chemokine receptor binding heterocyclic compounds

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Quick Facts

Patent No.: US 7,629,337
App. No.: 11/494,943
Granted: Dec 8, 2009
Kind: B2

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Abstract

Heterocyclic compounds that bind chemokine receptors and inhibit the binding of their natural ligands are disclosed. The invention compounds are protective against infection by HIV and exert effects characteristic of antagonists to the CXCR 4 receptor.

Claims (112)

1. A method to treat HIV or rheumatoid arthritis in a human or animal subject, comprising administering to a subject in need of such treatment an effective amount of a compound of formula I

or pharmaceutically acceptable acid addition salts, and any stereoisomeric forms and mixtures of stereoisomeric forms thereof;

wherein, W is a nitrogen atom and Y is void or, W is a carbon atom and Y═H;

R 1 to R 7 may be the same or different and are independently selected from hydrogen or straight, branched or cyclic C 1-6 alkyl, where R 1 and R 2 together may form ═O;

R 8 is an optionally substituted heterocyclic group or an optionally substituted aromatic group;

Ar is an aromatic or heteroaromatic ring each optionally substituted at single or multiple, non-linking positions with electron-donating or withdrawing groups;

n and n′ are independently 0-2;

X is a group of the formula:

wherein Ring A is an optionally substituted pyridine ring, and P is the nitrogen atom of said pyridine ring;

Ring A is bound to group W from any position through group V;

wherein V is a chemical bond or V is a (CH 2 ) n″ group, (where n″=0-2) or V is a C═O group; and

wherein Z is selected from the group consisting of: a hydrogen atom; an optionally substituted C 1-6 alkyl group; a C 0-6 alkyl group substituted with an optionally substituted aromatic or heterocyclic group; and an optionally substituted C 0-6 alkylamino or C 3-7 cycloalkylamino group;

thereby treating HIV or rheumatoid arthritis in said subject.

2. The method of claim 1 , comprising administering the compound of formula I in a subject, thereby treating HIV.

3. The method of claim 1 , comprising administering the compound of formula I and one or more agents useful in the treatment of HIV for treating HIV.

4. The method of claim 3 , wherein said one or more agents are selected from the group consisting of: nucleotide reverse transcriptase inhibitor such as zidovudine, didanosine, lamivudine, zalcitabine, abacavir, stavudine, adefovir, adefovir dipivoxil, fozivudine todoxil; non-nucleotide reverse transcriptase inhibitor such as nevirapine, delavirdine, efavirenz, loviride, immunocal, or oltipraz; and protease inhibitors such as saquinavir, ritonavir, indinavir, nelfinavir, amprenavir, palinavir, and lasinavir.

5. The method of claim 1 , wherein said compound is selected from the group consisting of:

AMD7130,N,N′-bis(2-pyridinylmethyl)-N-[1-(N″-phenyl-N″-methylureido) -4-piperidinyl]-1,3-benzenedimethanamine;

AMD7131,N,N′-bis(2-pyridinylmethyl)-N-[(N″-p-toluenesulfonylphenylalanyl) -4-piperidinyl]-1,3-benzenedimethanamine;

AMD7136,N,N′-bis(2-pyridinylmethyl)-N-[1-[3-(2-chlorophenyl)-5-methyl-isoxazol-4-oyl]-4-piperidinyl]-1,3-benzenedimethanamine;

AMD7147,N-[(1-methyl-2-carboxamido)ethyl]-N,N′-bis(2-pyridinylmethyl) -1,3-benzenedimethanamine;

AMD7156,N-[1-(benzyl)-3-pyrrolidinyl]-N,N′-bis(2-pyridinylmethyl) -1,3-benzenedimethanamine;

AMD7159,N-[[1-methyl-3-(pyrazol-3-yl)]propyl]-N,N′-bis(2-pyridinylmethyl) -1,3-benzenedimethanamine;

AMD7160,N-[1-(phenyl)ethyl]-N,N′-bis(2-pyridinylmethyl)-1,3-benzenedimethanamine;

AMD7166,N-[1-benzyl-3-carboxymethyl-4-piperidinyl]-N,N′-bis(2-pyridinylmethyl) -1,3-benzenedimethanamine;

AMD7169,N-[[1-methyl-2-(2-tolyl)carboxamido]ethyl]-N,N′-bis(2-pyridinylmethyl) -1,3-benzenedimethanamine;

AMD7177,N-[1H-imidazol-4-ylmethyl]-N,N′-bis(2-pyridinylmethyl) -1,3-benzenedimethanamine;

AMD7197,N,N′-bis(2-pyridinylmethyl)-N-[1-(N″-phenyl-N″-methylureido) -4-piperidinyl]-1,4-benzenedimethanamine;

AMD7198,N,N′-bis(2-pyridinylmethyl)-N-[N″-p-toluenesulfonylphenylalanyl) -4-piperidinyl]-1,4-benzenedimethanamine;

AMD7199,N-[1-(3-pyridinecarboxamido)-4-piperidinyl]-N,N′-bis(2-pyridinylmethyl) -1,4-benzenedimethanamine;

AMD7200,N-[1-(cyclopropylcarboxamido)-4-piperidinyl]-N,N′-bis(2-pyridinylmethyl) -1,4-benzenedimethanamine;

AMD7201,N-[1-(1-phenylcyclopropylcarboxamido)-4-piperidinyl]-N,N′-bis(2-pyridinylmethyl)-1,4-benzenedimethanamine.;

AMD7203,N-[1-[3-(2-chlorophenyl)-5-methyl-isoxazol-4-carboxamido]-4-piperidinyl]-N,N′-bis(2-pyridinylmethyl)-1,4-benzenedimethanamine;

AMD7204,N-[1-(2-thiomethylpyridine-3-carboxamido)-4-piperidinyl]-N,N′-bis(2-pyridinylmethyl)-1,4-benzenedimethanamine;

AMD7217,N-[2-(N″-morpholinomethyl)-1-cyclopentyl]-N,N′-bis(2-pyridinylmethyl) -1,4-benzenedimethanamine;

AMD7220,N-[(1-methyl-3-piperidinyl)propyl]-N,N′-bis(2-pyridinylmethyl) -1,4-benzenedimethanamine;

AMD7223,N-[1-(benzyl)-3-pyrrolidinyl]-N,N′-bis(2-pyridinylmethyl) -1,4-benzenedimethanamine;

AMD7228,N-[[(1-phenyl-3-(N″-morpholino)]propyl]-N,N′-bis(2-pyridinylmethyl) -1,4-benzenedimethanamine;

AMD7229,N-[1-(iso-propyl)-4-piperidinyl]-N,N′-bis(2-pyridinylmethyl) -1,4-benzenedimethanamine;

AMD7235,N-[1-methyl-2-(N″,N″-diethylcarboxamido)ethyl]-N,N′-bis(2-pyridinylmethyl)-1,4-benzenedimethanamine;

AMD7250,N-[1H-imidazol-2-ylmethyl]-N,N′-bis(2-pyridinylmethyl) -1,4-benzenedimethanamine;

AMD7254:N-[(5-benzyloxy)benzo[b]pyrrol-3-ylmethyl]-N,N′-bis(2-pyridinylmethyl)-1,4-benzenedimethanamine;

AMD7257,N-[(4-methyl)-1H-imidazol-5-ylmethyl]-N,N′-bis(2-pyridinylmethyl) -1,4-benzenedimethanamine;

AMD7259:N-[[(4-dimethylamino)-1-napthalenyl]methyl]-N,N′-bis(2-pyridinylmethyl)-1,4-benzenedimethanamine;

AMD7260,N-[1,5-dimethyl-2-phenyl-3-pyrazolinone-4-ylmethyl]-N,N′-bis(2-pyridinylmethyl)-1,4-benzenedimethanamine;

AMD7261,N-[1-[(1-acetyl-2-(R)-prolinyl]-4-piperidinyl]-N-[2-(2-pyridinyl)ethyl]-N′-(2-pyridinylmethyl)-1,3-benzenedimethanamine;

AMD7262,N-[1-[2-acetamidobenzoyl-4-piperidinyl]-4-piperidinyl]-N-[2-(2-pyridinyl)ethyl]-N′-(2-pyridinylmethyl)-1,3-benzenedimethanamine;

AMD7272,N-[(N″-acetyltryptophanyl)-4-piperidinyl]-N-[2-(2-pyridinyl)ethyl]-N′-(2-pyridinylmethyl)-1,3-benzenedimethanamine;

AMD7273,N-[(N″-benzoylvalinyl)-4-piperidinyl]-N-[2-(2-pyridinyl)ethyl]-N′-(2-pyridinylmethyl)-1,3-benzenedimethanamine;

AMD7277,N-[1-butyl-4-piperidinyl]-N-[2-(2-pyridinyl)ethyl]-N′-(2-pyridinylmethyl) -1,3-benzenedimethanamine;

AMD7278,N-[1-benzoyl-4-piperidinyl]-N-[2-(2-pyridinyl)ethyl]-N′-(2-pyridinylmethyl) -1,3-benzenedimethanamine;

AMD7309:N-[(1-methyl)benzo[b]pyrrol-3-ylmethyl]-N-[2-(2-pyridinyl)ethyl]-N′-(2-pyridinylmethyl)-1,3-benzenedimethanamine;

AMD7311,N-[1H-imidazol-4-ylmethyl]-N-[2-(2-pyridinyl)ethyl]-N′-(2-pyridinylmethyl) -1,3-benzenedimethanamine;

AMD7359,N-[1-(benzyl)-4-piperidinyl]-N-[2-(2-pyridinyl)ethyl]-N′-(2-pyridinylmethyl) -1,4-benzenedimethanamine;

AMD7374:N-[1-methylbenzimidazol-2-ylmethyl]-N-[2-(2-pyridinyl)ethyl]-N′-(2-pyridinylmethyl)-1,4-benzenedimethanamine; and

AMD7379:N-[(2-phenyl)benzo [b]pyrrol-3-ylmethyl]-N-[2-(2-pyridinyl)ethyl]-N′-(2-pyridinylmethyl)-1,4-benzenedimethanamine; or a pharmaceutically acceptable salt thereof.

6. The method of claim 1 , wherein said subject is a mammalian subject.

7. The method of claim 1 , comprising administering the compound of formula I in a subject, thereby treating rheumatoid arthritis.

8. A compound of formula I

or pharmaceutically acceptable acid addition salts, and any stereoisomeric forms and mixtures of stereoisomeric forms thereof;

wherein, W is a nitrogen atom and Y is void or, W is a carbon atom and Y═H;

R 1 to R 7 may be the same or different and are independently selected from hydrogen or straight, branched or cyclic C 1-6 alkyl, where R 1 and R 2 together may form ═O;

R 8 is an optionally substituted heterocyclic group or an optionally substituted aromatic group;

Ar is an aromatic or heteroaromatic ring each optionally substituted at single or multiple, non-linking positions with electron-donating or withdrawing groups;

n and n′ are independently, 0-2;

X is a group of the formula:

wherein Ring A is an optionally substituted pyridine ring, and P is the nitrogen atom of said pyridine ring;

Ring A is bound to group W from any position through group V;

wherein V is a chemical bond or V is a (CH 2 ) n″ group, (where n″=0-2) or V is a C═O group; and

9. The compound of claim 8 , selected from the group consisting of:

AMD7130,N,N′-bis(2-pyridinylmethyl)-N-[1-(N″-phenyl-N″-methylureido) 4-piperidinyl]-1,3-benzenedimethanamine;

AMD7131,N,N′-bis(2-pyridinylmethyl)-N-[(N″-p-toluenesulfonylphenylalanyl) -4-piperidinyl]-1,3-benzenedimethanamine;

AMD7136,N,N′-bis(2-pyridinylmethyl)-N-[1-[3-(2-chlorophenyl)-5 -methyl-isoxazol-4-oyl]-4-piperidinyl]-1,3-benzenedimethanamine;

AMD7147,N-[(1-methyl-2-carboxamido)ethyl]-N,N′-bis(2-pyridinylmethyl) -1,3-benzenedimethanamine;

AMD7156,N-[1-(benzyl)-3-pyrrolidinyl]-N,N′-bis(2-pyridinylmethyl) -1,3-benzenedimethanamine;

AMD7159,N-[[1-methyl-3-(pyrazol-3-yl)]propyl]-N,N′-bis(2-pyridinylmethyl) -1,3-benzenedimethanamine;

AMD7160,N-[1-(phenyl)ethyl]-N,N′-bis(2-pyridinylmethyl)-1,3-benzenedimethanamine;

AMD7166,N-[1-benzyl-3-carboxymethyl-4-piperidinyl]-N,N′-bis(2-pyridinylmethyl) -1,3-benzenedimethanamine;

AMD7169,N-[[1-methyl-2-(2-tolyl)carboxamido]ethyl]- N,N′-bis(2-pyridinylmethyl) -1,3-benzenedimethanamine;

AMD7177,N-[1H-imidazol-4-ylmethyl]-N,N′-bis(2-pyridinylmethyl) -1,3-benzenedimethanamine;

AMD7197,N,N′-bis(2-pyridinylmethyl)-N-[1-(N″-phenyl-N″-methylureido) -4-piperidinyl]-1,4-benzenedimethanamine;

AMD7198,N,N′-bis(2-pyridinylmethyl)-N-[N″-p-toluenesulfonylphenylalanyl) -4-piperidinyl]-1,4-benzenedimethanamine;

AMD7199,N-[1-(3-pyridinecarboxamido)-4-piperidinyl]-N,N′-bis(2-pyridinylmethyl) -1,4-benzenedimethanamine;

AMD7200,N-[1-(cyclopropylcarboxamido)-4-piperidinyl]-N,N′-bis(2-pyridinylmethyl) -1,4-benzenedimethanamine;

AMD7201,N-[l -(1 -phenylcyclopropylcarboxamido)-4-piperidinyl]-N,N′-bis(2-pyridinylmethyl)-1,4-benzenedimethanamine.;