IP Library › Granted Patent US 7,985,752
Granted Patent B2
US 7,985,752 · App. 12/474,943 · Granted Jul 26, 2011

Phenyl piperazine compounds, pharmaceutical composition including the same and use thereof

Assignee: SK Holdings Co., Ltd.
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Quick Facts
Patent No.
US 7,985,752
App. No.
12/474,943
Granted
Jul 26, 2011
Kind
B2
Abstract

The present invention relates to novel piperazine derivatives or pharmaceutically acceptable salts thereof, a process for preparing the same, and in particular, a high binding for Serotonin 1A(5-hydroxytryptamine; 5-HT1A) receptor, a pharmaceutical composition for treatment and/or prevention of depression and anxiety including an effective amount of the piperazine compound, and a method of treating depression, anxiety and other conditions related to 5-HT1A receptor in a mammal.

Claims (40)

1. A piperazine compound represented by Formula (I):

or pharmaceutically acceptable salts thereof, wherein

n is an integer from 2 to 6;

R1 and R2 are the same or different and are independently selected from the group consisting of hydrogen, a hydroxyl group, a halogen, nitrogen dioxide, a straight or branched chain alkyl group with 1 to 4 carbon atoms, and a straight or branched chain alkoxy group with 1 to 4 carbon atoms;

R3 is a C1-C2 alkylene; and

R4 is selected from the group consisting of:

(a) a C2-C6 dialkylamine,

(b) a 5 to 9-membered aromatic amine wherein the ring is independently substituted with at least one of hydrogen, a C1-C6 aliphatic alkyl, a C3 to C10 cyclic alkyl, a C6-C10 aryl group and a halogen,

(c) a 5 to 9-membered heteroaromatic amine comprising at least a nitrogen atom as a ring constituent wherein the ring is independently substituted with at least one of hydrogen, a C1-C6 aliphatic alkyl, a C3 to C10 cyclic alkyl, a C6-C10 aryl group and a halogen,

(d) a 5 to 9-membered heterocyclic ring comprising at least a nitrogen atom as a ring constituent wherein the ring is independently substituted with at least one of hydrogen, a C1-C6 aliphatic alkyl, a C3 to C10 cyclic alkyl, a C6-C10 aryl group and a halogen, and

(e) a 5 to 9-membered heteroaromatic ring comprising at least a nitrogen atom as a ring constituent wherein the ring is independently substituted with at least one of hydrogen, a C1-C6 aliphatic alkyl, a C3 to C10 cyclic alkyl, a C6-C10 aryl group and a halogen; and

R4 is connected to R3 group through a nitrogen atom therein,

wherein R4 is not morpholine.

2. The piperazine compound of claim 1 , wherein R4 is dimethylamine or diethylamine.

3. The piperazine compound of claim 1 , wherein R4 is connected to R3 through a nitrogen atom in an amino group of the 5 to 9-membered aromatic amine or heteroaromatic amine.

4. The piperazine compound of claim 3 , wherein R4 is a 5 or 6-membered aromatic amine substituted with at least one of hydrogen, a C1-C6 alkyl, and a halogen.

5. The piperazine compound of claim 4 , wherein R4 is a 6-membered aromatic amine substituted with hydrogen.

6. The piperazine compound of claim 3 , wherein R4 is a 5 or 6-membered heteroaromatic amine substituted with at least one of a C1-C6 alkyl and a halogen, wherein the heteroaromatic amine comprises at least two heteroatoms as ring constituents where a first heteroatom is N and a second heteroatom is independently selected from the group consisting of N, O, and S.

7. The piperazine compound of claim 6 , wherein R4 is a 5-membered heteroaromatic amine having a structure (II) selected from the group consisting of:

8. The piperazine compound of claim 1 , wherein R4 is connected to R3 through a nitrogen atom contained in a ring as a heteroatom of the 5 to 9-membered heterocyclic ring or heteroaromatic ring.

9. The piperazine compound of claim 8 , wherein R4 is a 5 or 6-membered heterocyclic ring having a structure (III) selected from the group consisting of:

10. The piperazine compound of claim 8 , wherein R4 is an azole selected from the group consisting of diazole, triazole, tetraazol, benzotriazole, imidazole, pyrazole, benzimidazloe, and indazole.

11. The piperazine compound of claim 10 , wherein the azole has a structure (IV) selected from the group consisting of:

12. The piperazine compound of claim 1 , wherein R1 and R2 are independently selected from the group consisting of hydrogen, a halogen, a straight or branched chain alkyl group with 1 to 4 carbon atoms, and a straight or branched chain alkoxy group with 1 to 4 carbon atoms.

13. The piperazine compound of claim 1 , wherein said compound is selected from the group consisting of: 1-[4-(4-imidazol-1-ylmethyl-phenoxy)-butyl]-4-(2-methoxy-phenyl)-piperazine, 1-(2-methoxy-phenyl)-4-[4-(4-[1,2,4]triazol-1-ylmethyl-phenoxy)-butyl]-piperazine, 1-(2-methoxy-phenyl)-4-[4-(4-tetrazol-1-ylmethyl -phenoxy)-butyl]-piperazine, 1-(2-methoxy-phenyl)-4-[4-(4-tetrazol-2-ylmethyl -phenoxy)-butyl]-piperazine, 1-[4-(3-imidazol-1-ylmethyl-phenoxy)-butyl]-4-(2-methoxy-phenyl)-piperazine-hydrochloride, 1-(2-methoxy-phenyl)-4-[4-(3-[1,2,4]triazol-1-ylmethyl-phenoxy)-butyl]-piperazine hydrochloride, 1-(2-methoxy-phenyl)-4-[4-(3-tetrazol-1-ylmethyl -phenoxy)-butyl]-piperazine hydrochloride, 1-(2-methoxy-phenyl)-4-[4-(3-tetrazol-2-ylmethyl -phenoxy)-butyl]-piperazine hydrochloride, 1-(4-{4-[4-(2-methoxy-phenyl)-piperazin-1-yl ]-butoxy}-benzyl)-1H-benzoimidazole, 1-(2-Methoxy-phenyl)-4-{4-[4-(2-methyl-imidazol-1-ylmethyl) -phenoxy]-butyl}-piperazine, 1-(2-methoxy-phenyl)-4-[4-(4-[1,2,3]triazol-2-ylmethyl-phenoxy) -butyl]-piperazine, 1-(2-methoxy-phenyl)-4-[4-(4-[1,2,3]triazol-1-ylmethyl-phenoxy) -butyl]-piperazine, 1-(4-{4-[4-(2-Methoxy-phenyl)-piperazin-1-yl]-butoxy}-benzyl)-1H-indazole, 1-(4-{4-[4-(2-Methoxy-phenyl)-piperazin-1-yl]-butoxy}-benzyl)-1H-benzotriazole, 1-(2-methoxy-phenyl)-4-{4-[4-(5-phenyl-tetrazol-2-ylmethyl)-phenoxy]-butyl}-piperazine, 1-(2-methoxy-phenyl)-4-{4-[4-(5-phenyl-tetrazol-1-ylmethyl)-phenoxy]-butyl}-piperazine, 1-(2-methoxy-phenyl)-4-{4-[4-(5-methyl-tetrazol-2-ylmethyl)-phenoxy]-butyl}-piperazine, 1-(2-methoxy-phenyl)-4-{4-[4-(5-methyl-tetrazol-1-ylmethyl)-phenoxy]-butyl}-piperazine, (4-{4-[4-(2-methoxy-phenyl)-piperazin-1-yl]-butoxy}-benzyl)-dimethyl-amine di-hydrochloride, 1-(2-methoxy-phenyl) -4-[4-(4-piperidin-1-ylmethyl-phenoxy)-butyl]-piperazine, (4-{4-[4-(2-methoxy-phenyl)-piperazin-1-yl]-butoxy}-benzyl)-phenyl-amine, (4-{4-[4-(2-methoxy-phenyl)-piperazin-1-yl]-butoxy}-benzyl)-thiazol-2-yl-amine, 1-(2-chloro-phenyl)-4-[4-(4-[1,2,4]triazol-1-ylmethyl-phenoxy)-butyl]-piperazine, 1-(2-methoxy-phenyl)-4-[4-(3-[1,2,3]triazol-2-ylmethyl-phenoxy)-butyl]-piperazine, 1-(2-Methoxy-phenyl)-4-[4-(3-[1,2,3]triazol-1-ylmethyl-phenoxy)-butyl]-piperazine, 1-(2-Methoxy-phenyl)-4-[4-(3-[1,2,3]triazol-2-ylmethyl-phenoxy)-butyl]-piperazine, 1-(2-methoxy-phenyl)-4-{4-[3-(5-methyl-tetrazol-1-ylmethyl)-phenoxy]-butyl}-piperazine, (3-{4-[4-(2-methoxy-phenyl)-piperazin-1-yl]-butoxy}-benzyl)-dimethyl-amine, 1-{4-[4-(4,5-dichloro-imidazol-1-ylmethyl)-phenoxy ]-butyl}-4-(2-methoxy-phenyl)-piperazine, 1-(2-chloro-phenyl)-4-[4-(4-tetrazol-2-ylmethyl-phenoxy)-butyl]-piperazine, (4-{4-[4-(2-Chloro-phenyl)-piperazin-1-yl]-butoxy}-benzyl)-dimethyl-amine, 1-(3-fluoro-phenyl)-4-[4-(4-[1,2,4]triazol-1-ylmethyl -phenoxy)-butyl]-piperazine, 1-(2-methoxy-phenyl)-4-[4-(4-4-methylpiperazine-1-ylmethyl-phenoxy) -butyl]-piperazine, 1-(2,3-dichloro-phenyl)-4-[4-(4-tetrazol-2-ylmethyl-phenoxy)-butyl ]-piperazine, 1-(2,3-Dichloro-phenyl)-4-{4-[4-(5-methyl-tetrazol-1-ylmethyl)-phenoxy]-butyl }-piperazine, 1-(2,3-Dichloro-phenyl)-4-{4-[4-(5-methyl-tetrazol-2-ylmethyl) -phenoxy]-butyl}-piperazine, (4-{4-[4-(2,3-dichloro-phenyl)-piperazin-1-yl]-butoxy}-benzyl)-dimethyl -amine, 1-(2-methoxy-phenyl)-4-[4-(4-4-methylpiperazine-1-ylmethyl-phenoxy)-butyl]-piperazine, 1-(2-chloro-phenyl)-4-[4-(4-[1,2,3]triazol-1-ylmethyl-phenoxy)-butyl]-piperazine, (4-{4-[4-(2-Methoxy-phenyl)-piperazin-1-yl]-butoxy}-benzyl)-[1,3,4]thiadiazol-2-yl-amine, 1-(2,3-dichloro-phenyl)-4-[4-(4-[1,2,3]triazol-1-ylmethyl-phenoxy)-butyl]-piperazine, (4-{4-[4-(2-Methoxy-phenyl)-piperazin-1-yl]-butoxy}-benzyl)-(5-methyl-isoxazol-3-yl)-amine, (4-{4-[4-(2-methoxy-phenyl)-piperazin-1-yl]-butoxy}-benzyl)-(5-methyl-isoxazol-3-yl)-amine, 1-{4-[4-(2-imidazol-1-yl-ethyl)-phenoxy]-butyl}-4-(2-methoxy-phenyl)-piperazine, 1-(2-methoxy-phenyl)-4-{4-[4-(2-[1,2,4]triazol-1-yl-ethyl)-phenoxy]-butyl}-piperazine, 1-(2-methoxy-phenyl)-4-{4-[4-(2-[1,2,3]triazol-2-yl-ethyl)-phenoxy]-butyl}-piperazine, 1-(2-methoxy-phenyl)-4-{4-[4-(2-[1,2,3]triazol-1-yl-ethyl)-phenoxy]-butyl}-piperazine, 1-(2-methoxy-phenyl)-4-{4-[4-(2-tetrazol-2-yl-ethyl)-phenoxy]-butyl}-piperazine, 1-(2-methoxy-phenyl)-4-{4-[4-(2-tetrazol-1-yl-ethyl)-phenoxy]-butyl}-piperazine, 1-(2-Methoxy-phenyl)-4-(4-{4-[2-(5-methyl-tetrazol-1-yl)-ethyl]-phenoxy}-butyl)-piperazine, 1-(2-Methoxy-phenyl)-4-(4-{4-[2-(5-methyl-tetrazol-2-yl)-ethyl]-phenoxy}-butyl)-piperazine, 2-{4-[4-(4-[1,2,3]-triazol-1-ylmethyl-phenoxy)-butyl]-piperazin-1-yl}-benzonitrile, and 1-(2-chloro-phenyl)-4-[4-(4-[1,2,3]triazol-2-ylmethyl-phenoxy)-butyl]-piperazine.

14. A pharmaceutical composition comprising:

(A) an effective amount of a piperazine compound represented by Formula (I):

or pharmaceutically acceptable salts thereof, wherein

n is an integer from 2 to 6;

R1 and R2 are the same or different and are independently selected from the group consisting of hydrogen, a hydroxyl group, a halogen, nitrogen dioxide, a straight or branched chain alkyl group with 1 to 4 carbon atoms, and a straight or branched chain alkoxy group with 1 to 4 carbon atoms;

R3 is a C1-C2 alkylene; and

R4 is selected from the group consisting of:

(a) a C2-C6 dialkylamine,

(b) a 5 to 9-membered aromatic amine wherein the ring is independently substituted with at least one of hydrogen, a C1-C6 aliphatic alkyl, a C3 to C10 cyclic alkyl, a C6-C10 aryl group and a halogen,

(c) a 5 to 9-membered heteroaromatic amine comprising at least a nitrogen atom as a ring constituent wherein the ring is independently substituted with at least one of hydrogen, a C1-C6 aliphatic alkyl, a C3 to C10 cyclic alkyl, a C6-C10 aryl group and a halogen,

(d) a 5 to 9-membered heterocyclic ring comprising at least a nitrogen atom as a ring constituent wherein the ring is independently substituted with at least one of hydrogen, a C1-C6 aliphatic alkyl, a C3 to C10 cyclic alkyl, a C6-C10 aryl group and a halogen, and

(e) a 5 to 9-membered heteroaromatic ring comprising at least a nitrogen atom as a ring constituent wherein the ring is independently substituted with at least one of hydrogen, a C1-C6 aliphatic alkyl, a C3 to C10 cyclic alkyl, a C6-C10 aryl group and a halogen; and

R4 is connected to R3 group through a nitrogen atom therein; and

(B) a pharmaceutically acceptable carrier or excipient,

wherein R4 is not morpholine.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE MAILING ADDRESS COUNTRY OF THE ASSIGNEE PREVIOUSLY RECORDED ON REEL 026892 FRAME 0846. ASSIGNOR(S) HEREBY CONFIRMS THE MAILING ADDRESS COUNTRY OF THE ASSIGNEE SHOULD BE CHANGED FROM "KOREA, DEMOCRATIC PEOPLE'S REPUBLIC OF" TO "KOREA, REPUBLIC OF". Recorded Nov 6, 2013
From: SK HOLDINGS CO., LTD.
To: SK BIOPHARMACEUTICALS CO., LTD.
Reel/Frame 031589/0390 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 13, 2011
From: SK HOLDINGS CO., LTD.
To: SK BIOPHARMACEUTICALS CO., LTD.
Reel/Frame 026892/0846 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 12, 2009
From: KIM, YONGGIL; CHO, NAHMRYUNE; KIM, YUNHEE; HEO, JOON; DONG, SEONMIN; JI, MI KYUNG; CHA, MAN-YOUNG; LEE, KIHO
To: SK HOLDINGS CO., LTD.
Reel/Frame 023091/0715 →
Continuity (2)
Continuation In Part 12128999 · May 29, 2008
Related Publication 20090298831A1 · Dec 3, 2009