IP Library Granted Patent US 8,759,352
Granted Patent B2
US 8,759,352 · App. 13/060,730 · Granted Jun 24, 2014

1-(4-ureidobenzoyl)piperazine derivatives

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Quick Facts
Patent No.
US 8,759,352
App. No.
13/060,730
Granted
Jun 24, 2014
Kind
B2
Abstract

The present invention relates to 1-(4-ureidobenzoyl)piperazine derivatives having the general Formula I (We bring to your attention that formula I is not provided on this electronic version as it is provided in the abstract of the paper copy) Wherein R 1 is (C 1-8 )alkyl, (C 3-8 )cycloalkyl or (C 3-8 )cycloalkyl(C 1-3 )alkyl, each of which may be substituted by hydroxy, cyano or halogen; R 2 represents 1 or 2 optional halogens; R 3 is (C 1-6 )alkyl, (C 3-6 )cycloalkyl or (C 3-6 )cycloalkyl(C 1-3 )alkyl, each of which may be substituted by one or more halogens; A represents a heteroaryl ring system comprising 1-3 heteroatoms selected from N, O and S, which ring system is 5- or 6-membered when X is C, and 5-membered when X is N; n is 1 or 2; or a pharmaceutically acceptable salt thereof; to pharmaceutical compositions comprising the same, and to the use of a these 1-(4-ureidobenzoyl)piperazine derivatives for the manufacture of a medicament for treating or preventing atherosclerosis and related disorders associated with cholesterol and bile acids transport and metabolism.

Claims (36)

1. A 1-(4-ureidobenzoyl)piperazine derivative having the general formula I

wherein

R 1 is (C 1-8 )alkyl, (C 3-8 )cycloalkyl or (C 3-8 )cycloalkyl(C 1-3 )alkyl, each of which may be substituted by hydroxy, cyano or halogen;

R 2 represents 1 or 2 optional halogens;

R 3 is (C 1-6 )alkyl, (C 3-6 )cycloalkyl or (C 3-6 )cycloalkyl(C 1-3 )alkyl, each of which may be substituted by one or more halogens;

A represents a heteroaryl ring system comprising 1-3 heteroatoms selected from N, O and S, which ring system is 5- or 6-membered when X is C, and 5-membered when X is N; n is 1 or 2; or a pharmaceutically acceptable salt thereof.

2. The 1-(4-ureidobenzoyl)piperazine derivative of claim 1 , wherein A represents furan-2,5-diyl or pyridine-2,6-diyl.

3. The 1-(4-ureidobenzoyl)piperazine derivative of claim 1 , wherein R 2 represents 1 or 2 halogens selected from F and Cl.

4. The 1-(4-ureidobenzoyl)piperazine derivative of claim 1 , wherein R 3 is tert-butyl.

5. The 1-(4-ureidobenzoyl)piperazine derivative of claim 1 , which is selected from:

N-tert-butyl-5-((4-(4-(3-cyclobutylureido)-3-fluorobenzoyl)piperazin-1-yl)methyl)furan-2-carboxamide;

N-tert-butyl-5-((4-(3-fluoro-4-(3-isobutylureido)benzoyl)piperazin-1-yl)methyl)furan-2-carboxamide;

N-tert-butyl-5-((4-(4-(3-(cyclopropylmethyl)ureido)-3-fluorobenzoyl)piperazin-1-yl)methyl)furan-2-carboxamide;

N-tert-butyl-5-((4-(3-fluoro-4-(3-neopentylureido)benzoyl)piperazin-1-yl)methyl)furan-2-carboxamide;

N-tert-butyl-5-((4-(3-fluoro-4-(3-isopentylureido)benzoyl)piperazin-1-yl)methyl)furan-2-carboxamide;

N-tert-butyl-5-((4-(4-(3-butylureido)-3-fluorobenzoyl)piperazin-1-yl)methyl)furan-2-carboxamide hydrochloride;

N-tert-butyl-5-((4-(3-chloro-4-(3-neopentylureido)benzoyl)piperazin-1-yl)methyl)furan-2-carboxamide;

N-tert-butyl-5-((4-(3-chloro-4-(3-isobutylureido)benzoyl)piperazin-1-yl)methyl)furan-2-carboxamide;

N-tert-butyl-5-((4-(3-chloro-4-(3-(cyclopropylmethyl)ureido)benzoyl)piperazin-1-yl)methyl)furan-2-carboxamide;

N-tert-butyl-5-((4-(3-chloro-4-(3-cyclobutylureido)benzoyl)piperazin-1-yl)methyl)furan-2-carboxamide;

N-tert-butyl-5-((4-(3-chloro-4-(3-isopentylureido)benzoyl)piperazin-1-yl)methyl)furan-2-carboxamide;

N-tert-butyl-5-((4-(4-(3-butylureido)-3-chlorobenzoyl)piperazin-1-yl)methyl)furan-2-carboxamide;

N-tert-butyl-5-((4-(4-(3-(cyclopropylmethyl)ureido)-2,3-difluorobenzoyl)piperazin-1-yl)methyl)furan-2-carboxamide;

N-tert-butyl-5-((4-(2,3-difluoro-4-(3-neopentylureido)benzoyl)piperazin-1-yl)methyl)furan-2-carboxamide;

N-tert-butyl-5-((4-(2,3-difluoro-4-(3-isobutylureido)benzoyl)piperazin-1-yl)methyl)furan-2-carboxamide;

N-tert-butyl-5-((4-(4-(3-cyclobutylureido)-2,3-difluorobenzoyl)piperazin-1-yl)methyl)furan-2-carboxamide;

N-tert-butyl-5-((4-(4-(3-butylureido)-2,3-difluorobenzoyl)piperazin-1-yl)methyl)furan-2-carboxamide;

N-tert-butyl-5-((4-(2,3-difluoro-4-(3-isopentylureido)benzoyl)piperazin-1-yl)methyl)furan-2-carboxamide;

N-tert-butyl-6-((4-(4-(3-cyclobutylureido)-3-fluorobenzoyl)piperazin-1-yl)methyl)picolinamide;

N-tert-butyl-6-((4-(3-fluoro-4-(3-neopentylureido)benzoyl)piperazin-1-yl)methyl)picolinamide;

N-tert-butyl-6-((4-(3-fluoro-4-(3-isopentylureido)benzoyl)piperazin-1-yl)methyl)picolinamide; and

N-tert-butyl-6-((4-(4-(3-(cyclopropylmethyl)ureido)-3-fluorobenzoyl)piperazin-1-yl)methyl)picolinamide; or a pharmaceutically acceptable salt thereof.

6. A pharmaceutical composition comprising a 1-(4-ureidobenzoyl)piperazine derivative of claim 1 or a pharmaceutically acceptable salt thereof and pharmaceutically acceptable auxiliaries.

7. A pharmaceutical composition comprising a 1-(4-ureidobenzoyl)piperazine derivative of claim 5 or a pharmaceutically acceptable salt thereof and pharmaceutically acceptable auxiliaries.

8. A method of treating atherosclerosis in a human patient in need of treatment comprising the administration of a therapeutically effective amount of a 1-(4-ureidobenzoyl)piperazine derivative of claim 1 or a pharmaceutically acceptable salt thereof.

9. A method of treating atherosclerosis in a human patient in need of treatment comprising the administration of a therapeutically effective amount of a 1-(4-ureidobenzoyl)piperazine derivative of claim 5 or a pharmaceutically acceptable salt thereof.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 12, 2014
From: COOKE, ANDREW JOHN; BENNETT, DAVID JONATHAN; EDWARDS, ANDREW STANLEY
To: N.V. ORGANON
Reel/Frame 032200/0936 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 12, 2014
From: ROUGHTON, ANDREW; NEAGU, IRINA; CHAN, JUI-HSIANG; HO, KOC-KAN; ANSARI, NASRIN; MORRIS, MICHELLE LEE; RONG, YAJING; OHLMEYER, MICHAEL
To: PHARMACOPEIA LLC.
Reel/Frame 032201/0085 →
MERGER Recorded Mar 8, 2013
From: ORGANON BIOSCIENCES NEDERLAND B.V.
To: MERCK SHARP & DOHME B.V.
Reel/Frame 029940/0296 →
MERGER Recorded Mar 7, 2013
From: MSD OSS B.V.
To: ORGANON BIOSCIENCES NEDERLAND B.V.
Reel/Frame 029939/0001 →
MERGER Recorded Dec 1, 2011
From: N.V. ORGANON
To: MSD OSS B.V.
Reel/Frame 027307/0482 →