Substituted aminobutyric derivatives as neprilysin inhibitors

Patent metadata

Field	Value
Publication number	US-9603819-B2
Application number	US-201514635311-A
Country	US
Kind code	B2
Filing date	Mar 2, 2015
Priority date	May 28, 2009
Publication date	Mar 28, 2017
Grant date	Mar 28, 2017

Abstract

The present invention provides a compound of formula I′;

or a pharmaceutically acceptable salt thereof, wherein R 1 , R 2 , R 3 , X and n are defined herein. The invention also relates to a method for manufacturing the compounds of the invention, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.

First claim

What is claimed is:

1. A compound of the formula (IIB):

or a pharmaceutically acceptable salt thereof, wherein:
R 1 is C 1-7 alkyl;
for each occurrence, R 2 is independently C 1-7 alkyl, NO 2 , CN, halo, C 3-7 cycloalkyl, hydroxy, C 1-7 alkoxy, halo-C 1-7 alkyl, NR b R c , C 6-10 aryl, heteroaryl or heterocyclyl; wherein R b and R c for each occurrence, are independently H or C 1-7 alkyl;
R 2a is halo;
X and X 1 are independently OH, —O—C 1-7 alkyl, —NR b R c , —NHS(O) 2 —C 1-7 alkyl, —NHS(O) 2 -benzyl or —O—C 6-10 aryl; wherein alkyl is optionally substituted with one or more substituents independently selected from the group consisting of aryl, heteroaryl, heterocyclyl, —C(O)NH 2 , —C(O)NH— C 1-6 alkyl, and —C(O)N(C 1-6 alkyl) 2 ;
A 1 is a bond or a linear C 1-4 alkylene substituted with one or more substituents independently selected from the group consisting of halo, O-acetate, C 1-7 alkyl and C 3-7 cycloalkyl; in which two geminal alkyl can optionally combine to form a C 3-7 cycloalkyl; or
p is 0, 1, 2, 3 or 4; and
wherein each heteroaryl is a monocyclic or bicyclic aromatic ring comprising 5-10 ring atoms selected from carbon atoms and 1 to 5 heteroatoms, and
each heterocyclyl is a monocyclic saturated or partially saturated but non-aromatic moiety comprising 4-7 ring atoms selected from carbon atoms and 1-5 heteroatoms, wherein each heteroatom of a heteroaryl or a heterocyclyl is independently selected from O, N and S.

2. The compound according to claim 1 , having Formula IIC

or a pharmaceutically acceptable salt thereof.

3. The compound according to claim 1 wherein A 1 has the following Formulae:

in which R d1 and R d2 are independently H, halo, C 3-7 cycloalkyl, or C 1-7 alkyl and at least one of R d1 and R d2 is other than H; and alternatively R d1 and R d2 can form together with the atoms to which they are attached a C 3-7 cycloalkyl; and
R e1 and R e2 are independently H, halo, C 3-7 cycloalkyl, or C 1-7 alkyl and at least one of R e1 and R e3 is other than H; and alternatively R e1 and R e2 can form together with the atoms to which they are attached a C 3-7 cycloalkyl; or a pharmaceutically acceptable salt thereof.

4. The compound according to claim 3 wherein A 1 is selected from the group consisting of:

or a pharmaceutically acceptable salt thereof.

5. The compound according to claim 1 wherein A 1 has the following Formula:

wherein R d3 , R d4 , R d5 and R d6 are independently H, halo, O-acetate or C 1-7 alkyl and at least one of R d3 , R d4 , R d5 and R d6 is other than H; or a pharmaceutically acceptable salt thereof.

6. The compound according to claim 5 wherein A 1 is selected from the group consisting of:

or a pharmaceutically acceptable salt thereof.

7. The compound according to claim 1 wherein each R 2 is independently halo, alkyl, alkoxy, hydroxy, haloalkyl; or a pharmaceutically acceptable salt thereof.

8. The compound according to claim 1 wherein X and X 1 are independently OH or —O—C 1-7 alkyl; or a pharmaceutically acceptable salt thereof.

9. A pharmaceutical composition comprising a compound according to claim 1 or a pharmaceutically acceptable salt thereof, and one or more pharmaceutically acceptable carriers.

10. A combination comprising: a compound according to claim 1 or a pharmaceutically acceptable salt thereof, and one or more therapeutically active agents selected from HMG-Co-A reductase inhibitor, an anigiotensin receptor blocker, angiotensin converting enzyme Inhibitor, a calcium channel blocker, an endothelin antagonist, a renin inhibitor, a diuretic, an ApoA-I mimic, an anti-diabetic agent, an obesity-reducing agent, an aldosterone receptor blocker, an endothelin receptor blocker, an aldosterone synthase inhibitors, a CETP inhibitor and a phosphodiesterase of type 5 (PDE5) inhibitor.

11. A method of inhibiting neutral endopeptidase EC. 3.4. 24.11. activity in a subject in need thereof, comprising: administering to the subject a therapeutically effective amount of the compound according to claim 1 ; or a pharmaceutically acceptable salt thereof.

12. A method of slowing or arresting the development of, or alleviating or ameliorating at least one physical parameter of, or stabilizing a discernible symptoms of a disorder or a disease associated with neutral endopeptidase EC. 3.4. 24.11. activity in a subject in need thereof, comprising: administering to the subject a therapeutically effective amount of the compound according to claim 1 ; or a pharmaceutically acceptable salt thereof; wherein the disorder or the disease is selected from hypertension, pulmonary hypertension, isolated systolic hypertension, resistant hypertension, peripheral vascular disease, heart failure, congestive heart failure, left ventricular hypertrophy, angina, renal insufficiency, renal failure, diabetic nephropathy, non-diabetic nephropathy, nephroic syndrome, glomerulonephritis, scleroderma, glomerular sclerosis, proteinurea of primary renal disease, renal vascular hypertention, diabetic retinopathy and end-stage renal disease (ESRD), endothelial dysfunction, diastolic dysfunction, hypertrophic cardiomyopathy, diabetic cardiac myopathy, supraventricular and ventricular arrhythmias, atrial fibrillation (AF), cardiac fibrosis, atrial flutter, detrimental vascular remodeling, plaque stabilization, myocardial infarction (MI), renal fibrosis, polycystic kidney disease (PKD), Pulmonary Arterial hypertension, renal failure, cyclical oedema, Menières disease, hyperaldosteroneism hypercalciuria, ascites, glaucoma, menstrual disorders, preterm labour, pre-eclampsia, endometriosis, reproductive disorders, asthma, obstructive sleep apnea, inflammation, leukemia, pain, epilepsy, affective disorders, depression and psychotic condition, dementia, geriatric confusion, obesity and gastrointestinal disorders, wound healing, septic shock, gastric acid secretion dysfunction, hyperreninaemia, cystic fibrosis, restenosis, type-2 diabetes, metabolic syndrome, diabetic complications, atherosclerosis, male and female sexual dysfunction.

13. A pharmaceutical composition comprising a compound according to claim 6 or a pharmaceutically acceptable salt thereof, and one or more pharmaceutically acceptable carriers.

14. A combination comprising: a compound according to claim 6 or a pharmaceutically acceptable salt thereof, and one or more therapeutically active agents selected from HMG-Co-A reductase inhibitor, an anigiotensin receptor blocker, angiotensin converting enzyme Inhibitor, a calcium channel blocker, an endothelin antagonist, a renin inhibitor, a diuretic, an ApoA-I mimic, an anti-diabetic agent, an obesity-reducing agent, an aldosterone receptor blocker, an endothelin receptor blocker, an aldosterone synthase inhibitors, a CETP inhibitor and a phosphodiesterase of type 5 (PDE5) inhibitor.

15. A method of inhibiting neutral endopeptidase EC. 3.4. 24.11. activity in a subject in need thereof, comprising: administering to the subject a thera

Assignees

• Novartis Ag

Inventors

• Coppola Gary Mark
• Iwaki Yuki
• Karki Rajeshri
• Kawanami Toshio
• Ksander Gary Michael
• Mogi Muneto
• Sun Robert

Classifications

• A61P9/00

  Drugs for disorders of the cardiovascular system · CPC title

• A61P3/10

  for hyperglycaemia, e.g. antidiabetics · CPC title

• A61P7/00

  Drugs for disorders of the blood or the extracellular fluid · CPC title

• A61P9/08

  Vasodilators for multiple indications · CPC title

• A61P9/04

  Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure · CPC title