IP Library Granted Patent US 10,087,151
Granted Patent B2
US 10,087,151 · App. 15/110,082 · Granted Oct 2, 2018

Substituted benzoxazine and related compounds

Inventors: Andrey S. Tsvetkov (Houston, TX); Steven M. Finkbeiner (Corte Madera, CA); Michael A. Pleiss (Sunnyvale, CA); Robert Greenhouse (Santa Clara, CA)
Assignee: THE J. DAVID GLADSTONE INSTITUTES, A TESTIMENTARY TRUST ESTABLISHED UNDER THE WILL OF J. DAVID GLADSTONE
C07D265/36A61K9/02A61K9/08A61K9/10A61K9/2059A61K9/4866C07D209/08C07D279/16C07D279/28C07D413/06C07D498/04
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Quick Facts
Patent No.
US 10,087,151
App. No.
15/110,082
Granted
Oct 2, 2018
Kind
B2
Abstract

The present invention relates to compounds including but not limited to of any one of formulas Ia, Ib, IIa, IIb, IIIa, IIIb, and IV to VI, VIIa, VIIb, VIIIa, VIIIb and VIIIc as described herein and their tautomers and/or pharmaceutically acceptable salts, compositions, and methods of uses thereof.

Claims (41)

1. A compound of formula V or VI:

wherein:

B 1 and B 2 are CR 2 ;

L is selected from the group consisting of a covalent bond, CR 6 2 , C(O)—(CR 6 2 ) m , C(S)—(CR 6 2 ) m , O—(CR 6 2 ) m , S—(CR 6 2 ) m , SO—(CR 6 2 ) m , SO 2 —(CR 6 2 ) m , and NR 6 —(CR 6 2 ) m ;

the variables m and p independently are 0, 1, 2, 3, 4, 5, 6, or 7;

R 1 is C 1 to C 6 alkyl, C 1 to C 6 haloalkyl, C 1 to C 6 alkoxy, C 1 to C 6 haloalkoxy, cyano, or nitro;

R 2 is hydrogen, C 1 to C 6 alkyl, C 1 to C 6 haloalkyl, C 1 to C 6 alkoxy, C 1 to C 6 haloalkoxy, halo, cyano, or nitro;

R 3 are independently hydrogen or C 1 to C 6 alkyl; or two R 3 together with the carbon attached thereto form C═O;

R 4 are independently C 1 to C 6 alkyl; or two R 4 together with the carbon attached thereto form C═O;

R 5 is hydrogen, C 1 to C 6 alkyl, substituted C 1 to C 6 alkyl, cycloalkyl, aryl, or acyl;

each R 6 independently is selected from the group consisting of hydrogen, halogen, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, alkenyl, substituted alkenyl, alkoxy, substituted alkoxy, alkynyl, substituted alkynyl, amino, substituted amino, aminosulfinyl substituted aminosulfinyl, aminosulfonyl, substituted aminosulfonyl, sulfinyl, sulfonyl, sulfonyloxy, substituted sulfonyloxy, aminosulfonyloxy, aminosulfinyloxy, aminosulfonylamino, acylamino, aminocarbonyloxy, aminocarbonylamino, aminothiocarbonylamino, amidino, substituted amidino, aminocarbonylamino, aminothiocarbonylamino, acyloxy, aryl, substituted aryl, heteroaryl, substituted heteroaryl, cyano, nitro, carboxyl, carboxyl ester, (carboxyl ester)amino, (carboxyl ester)oxy, hydroxyl, acyl, formyl, aminocarbonyl, substituted aminocarbonyl, and substituted aminothiocarbonyl, or two R 6 join together to form a ring selected from the group consisting of C 3 -C 7 cycloalkyl, C 3 -C 7 heterocycloalkyl, and substituted C 3 -C 7 heterocycloalkyl;

R 7 are independently hydrogen or C 1 to C 6 alkyl;

or a tautomer and/or a pharmaceutically acceptable salt thereof.

2. The compound of claim 1 selected from the group consisting of:

3. The compound according to claim 1 and selected from the group consisting of

1-(6-methyl-2,3-dihydro-4H-benzo[b][1,4]oxazin-4-yl)-2-(4-methylpiperazin-1-yl)ethan-1-one,

1-(6-methyl-2,3-dihydro-4H-benzo[b][1,4]oxazin-4-yl)-2-(4-phenylpiperazin-1-yl)ethan-1-one,

1-(6-methyl-2,3-dihydro-4H-benzo[b][1,4]oxazin-4-yl)-2-(piperazin-1-yl)ethan-1-one,

2-(4-acetylpiperazin-1-yl)-1-(6-methyl-2,3-dihydro-4H-benzo[b][1,4]oxazin-4-yl)ethan-1-one,

2-(6-methyl-2,3-dihydro-4H-benzo[b][1,4]oxazin-4-yl)-1-(4-methylpiperazin-1-yl)ethan-1-one,

6-methyl-4-(2-(4-methylpiperazin-1-yl)ethyl)-3,4-dihydro-2H-benzo[b][1,4]oxazine,

2-(4-cyclohexylpiperazin-1-yl)-1-(6-methyl-2,3-dihydro-1,4-benzoxazin-4-yl)ethanone,

1-(6-methyl-2,3-dihydro-1,4-benzoxazin-4-yl)-2-(4-propan-2-ylpiperazin-1-yl)ethanone,

1-[4-(2-hydroxyethyl)piperazin-1-yl]-2-(6-methyl-2,3-dihydro-1,4-benzoxazin-4-yl)ethanone,

1-[4-(2-methoxyethyl)piperazin-1-yl]-2-(6-methyl-2,3-dihydro-1,4-benzoxazin-4-yl)ethanone,

N-[2-[4-[2-(6-methyl-2,3-dihydro-1,4-benzoxazin-4-yl)acetyl]piperazin-1-yl]ethyl]methanesulfonamide,

or their tautomers and/or a pharmaceutically acceptable salt thereof.

4. A compound selected from the group consisting of

or their tautomers and/or a pharmaceutically acceptable salt thereof.

5. A pharmaceutical composition comprising a compound of claim 1 and a pharmaceutically acceptable excipient.

6. A method for inducing neuronal autophagy which method comprises contacting a cell with an effective amount of a compound of claim 1 , wherein the cell is selected from the group consisting of a neuron, microglia, macrophages, and astrocytes.

7. A method for treating a disease which method comprises administering to a patient an effective amount of a compound of claim 1 , wherein the disease is selected from the group consisting of Huntington's disease, spinocerebellar ataxias, Alzheimer's disease, Parkinson's disease, frontotemporal dementia, high-pressure neurological syndrome, dystonia, olivopontocerebellar atrophy, amyotrophic lateral sclerosis, multiple sclerosis, epilepsy, stroke, cerebral ischemia, hypoxia, multi-infarct dementia, cerebral trauma or damage, damage to the spinal cord, AIDS-dementia complex, viral or bacterial meningitis, poliomyelitis, Lyme disease, malaria, cancers with cerebral localization, Tourette's syndrome, hepatic encephalopathy, systemic lupus, analgesia, opiate-withdrawal symptoms, feeding behavior, schizophrenia, chronic anxiety, depressive disorders, disorders of the developing or aged brain alcoholism, nicotine addiction, illicit drug addiction, and type 2 diabetes.

8. A method for treating Huntington's disease, wherein the method comprises administering to a patient an effective amount of a compound of claim 1 .

9. The compound of claim 1 of formula V:

10. The compound of claim 9 wherein R 7 is hydrogen.

11. The compound of claim 9 wherein L is CR 6 2 or C(O)—(CR 6 2 ) m .

12. The compound of claim 9 wherein L is CR 6 2 or C(O).

13. A pharmaceutical composition comprising a compound of claim 9 and a pharmaceutically acceptable excipient.

14. A method for inducing neuronal autophagy which method comprises contacting a cell with an effective amount of a compound of claim 9 , wherein the cell is selected from the group consisting of a neuron, microglia, macrophages, and astrocytes.

15. A method for treating a disease which method comprises administering to a patient an effective amount of a compound of claim 9 , wherein the disease is selected from the group consisting of Huntington's disease, spinocerebellar ataxias, Alzheimer's disease, Parkinson's disease, frontotemporal dementia, high-pressure neurological syndrome, dystonia, olivopontocerebellar atrophy, amyotrophic lateral sclerosis, multiple sclerosis, epilepsy, stroke, cerebral ischemia, hypoxia, multi-infarct dementia, cerebral trauma or damage, damage to the spinal cord, AIDS-dementia complex, viral or bacterial meningitis, poliomyelitis, Lyme disease, malaria, cancers with cerebral localization, Tourette's syndrome, hepatic encephalopathy, systemic lupus, analgesia, opiate-withdrawal symptoms, feeding behavior, schizophrenia, chronic anxiety, depressive disorders, disorders of the developing or aged brain alcoholism, nicotine addiction, illicit drug addiction, and type 2 diabetes.

16. A method for treating Huntington's disease, wherein the method comprises administering to a patient an effective amount of a compound of claim 9 .

Assignments (1)
CONFIRMATORY LICENSE Recorded Jul 15, 2016
From: J. DAVID GLADSTONE INSTITUTES
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 039355/0617 →
Continuity (3)
Provisional Application 61927911 · Jan 15, 2014
Provisional Application 61925619 · Jan 9, 2014
Related Publication 20160326123A1 · Nov 10, 2016
Cited By (1)
US 12,264,167