IP Library Granted Patent US 8,013,003
Granted Patent B2
US 8,013,003 · App. 12/451,515 · Granted Sep 6, 2011

Di-substituted amides for enhancing glutamatergic synaptic responses

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Quick Facts
Patent No.
US 8,013,003
App. No.
12/451,515
Granted
Sep 6, 2011
Kind
B2
Abstract

This invention relates to compounds, pharmaceutical compositions and methods for use in the prevention and treatment of cerebral insufficiency, including enhancement of receptor functioning in synapses in brain networks responsible for basic and higher order behaviors. These brain networks, which are involved in regulation of breathing, and cognitive abilities related to memory impairment, such as is observed in a variety of dementias, in imbalances in neuronal activity between different brain regions, as is suggested in disorders such as Parkinson's disease, schizophrenia, respiratory depression, sleep apneas, attention deficit hyperactivity disorder and affective or mood disorders, and in disorders wherein a deficiency in neurotrophic factors is implicated, as well as in disorders of respiration such as overdose of an alcohol, an opiate, an opioid, a barbiturate, an anesthetic, or a nerve toxin, or where the respiratory depression results form a medical condition such as central sleep apnea, stroke-induced central sleep apnea, obstructive sleep apnea, congenital hypoventilation syndrome, obesity hypoventilation syndrome, sudden infant death syndrome, Rett syndrome, spinal cord injury, traumatic brain injury, Cheney-Stokes respiration, Ondines curse, Prader-Willi's syndrome and drowning. In a particular aspect, the invention relates to compounds useful for treatment of such conditions, and methods of using these compounds for such treatment.

Claims (153)

1. A compound according to the formula:

wherein:

W is oxygen;

X, Y and Z are each independently —CR,

wherein:

R is H, —Br, —Cl, —F, —CN, —NO 2 , —OR 1 , —SR 1 , —NR 1 2 , —C 1 -C 6 branched or un-branched alkyl, which may be un-substituted or substituted,

wherein:

R 1 is H, —C 1 -C 6 branched or un-branched alkyl which, may be un-substituted or substituted,

F═O or S,

A is H, or —C 1 -C 6 branched or un-branched alkyl, which may be un-substituted or substituted, —C 2 -C 6 branched or un-branched alkenyl, which may be un-substituted or substituted, —C 2 -C 6 branched or un-branched alkynyl, which may be un-substituted or substituted, —C 3 -C 7 cycloalkyl which may be un-substituted or substituted, —C 3 -C 7 alkylcycloalkyl which may be un-substituted or substituted, aryl or heterocycle which may be un-substituted or substituted, alkylaryl which may be un-substituted or substituted, alkylheterocycle which may be un-substituted or substituted

n=0, 1, 2, 3, 4, 5, or 6;

is a —C 3 -C 7 cycloalkyl which may be un-substituted or substituted, a —C 4 -C 7 azacycloalkyl, which may be un-substituted or substituted, a —C 7 -C 10 bicycloalkyl which may be un-substituted or substituted, a —C 7 -C 10 azabicycloalkyl which may be un-substituted or substituted, aryl which may be un-substituted or substituted or a heterocycle which may be un-substituted or substituted;

B is —C═, C—R a , O, N, S, C═O, S═O or SO 2 ;

R a is H, a halogen (preferably F), OH, Oalkyl, cyano, or a —C 1 -C 6 alkyl group which is un-substituted or substituted and which optionally, forms a C 3 -C 7 cycloalkyl group with D; and

D is absent when B is O, S, C═O, S═O or SO 2 , or if present, is bonded to B when B is —C═, —C—R a or N, and is H, a halogen (preferably F), OR b , a —C 1 -C 6 branched or un-branched alkyl, which may be un-substituted or substituted and which optionally, forms a C 3 -C 7 cycloalkyl group with R a , a

—C 2 -C 6 branched or un-branched alkenyl, which may be un-substituted or substituted, a —C 2 -C 6 branched or un-branched alkynyl, which may be un-substituted or substituted, a —C 3 -C 7 cycloalkyl which may be un-substituted or substituted, an aryl which may be un-substituted or substituted, a heterocycle which may be un-substituted or substituted, a —C 2 -C 7 carboxyalkyl which may be un-substituted or substituted, a carboxyaryl which may be un-substituted or substituted, a carboxyheteroaryl which may be un-substituted or substituted, a —C 1 -C 7 sulfonylalkyl which may be un-substituted or substituted, a sulfonylaryl which may be un-substituted or substituted or a sulfonylheteroaryl which may be un-substituted or substituted, or when B is —C—R a , R a and D optionally form a ═N—R c or a ═N—OR c group with B, wherein R c is H or an unsubstituted or substituted C 1 -C 7 alkyl group; and

R b is H, a —C 1 -C 7 alkyl group which may be branched or un-branched, un-substituted or substituted or a —C 2 -C 7 acyl group which may be un-substituted or substituted;

or a pharmaceutically acceptable salt or pro-drug thereof.

2. Compounds of claim 1 according to formula II:

wherein:

A is —C 1 -C 6 branched or un-branched alkyl, which may be un-substituted or substituted, a —C 3 -C 7 cycloalkyl which may be un-substituted or substituted;

n is 0, 1, 2, or 3; and

B is C—R a , C═O or O;

R a is H, OH, alkyl or F; and

D is absent, is H or OH when R a is H or alkyl, or is F when R a is F, or a pharmaceutically acceptable salt thereof.

3. Compounds of claim 1 according to formula III:

wherein:

A is a C 1 -C 6 alkyl which may be substituted or un-substituted

B is C—R a , O or C═O;

R a is H, F, —OH or alkyl and

D is absent (when B is O), is H or OH when R a is H or alkyl, or is F when R a is F, or a pharmaceutically acceptable salt thereof.

4. Compounds of claim 1 according to formula IV:

wherein:

A is a C 1 -C 6 alkyl which may be substituted or un-substituted,

n is 0, 1 or 2, or a pharmaceutically acceptable salt thereof.

5. Compounds of claim 1 according to formula V:

wherein:

A is a C 1 -C 6 alkyl which may be substituted or un-substituted,

R 1 is H, F, or C 1 -C 4 alkyl,

R 2 is H, F, CN, a heterocycle which may be substituted or un-substituted or OR 3 ,

R 3 is H, C 1 -C 6 alkyl which may be substituted or un-substituted, or a pharmaceutically acceptable salt thereof.

6. Compounds of claim 1 according to formula VI:

wherein:

A is a C 1 -C 6 alkyl which may be substituted or un-substituted,

R is H, or C 1 -C 4 alkyl, or a pharmaceutically acceptable salt thereof.

7. Compounds of claim 1 according to formula VII:

wherein:

B is C—R a , O or C═O;

R a is H, F, —OH or alkyl and

D is absent (when B is O), is H or OH when R a is H or alkyl, or is F when R a is F, or a pharmaceutically acceptable salt thereof.

8. Compounds of claim 1 according to formula VIII:

wherein:

B is C—R a , O or C═O;

R a is H, F, —OH or alkyl and

D is absent (when B is O), is H or OH when R a is H or alkyl, or is F when R a is F, or a pharmaceutically acceptable salt thereof.

9. Compounds of claim 1 according to formula IX:

wherein:

A is a C 1 -C 6 alkyl which may be substituted or un-substituted,

R 1 is H, or C 1 -C 4 alkyl,

R 2 is H, or a C 1 -C 6 alkyl which may be substituted or un-substituted,

R 3 is H, or a C 1 -C 6 alkyl which may be substituted or un-substituted,

R 4 is H, or a C 1 -C 6 alkyl which may be substituted or un-substituted, or a pharmaceutically acceptable salt thereof.

10. A compound according to claim 1 which is:

N-Cyclohexyl-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-Cyclopentyl-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-(trans-4-Cyanocyclohexyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-Methyl-N-tetrahydro-2H-pyran-4-yl-[2,1,3]-benzoxadiazole-5-carboxamide

N-Methyl-N-(4-oxocyclohexyl)-[2,1,3]-benzoxadiazole-5-carboxamide

N-(trans-4-Hydroxy-4-methylcyclohexyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide or

N-(4-trans-Hydroxycyclohexyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide.

11. A compound according to Formula IX of claim 9 which is:

trans-4-[(2,1,3-Benzoxadiazol-5-ylcarbonyl)(methyl)amino]cyclohexyl N,N-dimethyl glycinate hydrochloride

trans-4-[(2,1,3-Benzoxadiazol-5-ylcarbonyl)(methyl)amino]cyclohexyl L-alaninate hydrochloride

trans-4-[(2,1,3-Benzoxadiazol-5-ylcarbonyl)(methyl)amino]cyclohexyl L-valinate hydrochloride

trans-4-[(2,1,3-Benzoxadiazol-5-ylcarbonyl)(methyl)amino]-1-methylcyclohexyl N,N-dimethyl glycinate hydrochloride

trans-4-[(2,1,3-Benzoxadiazol-5-ylcarbonyl)(methyl)amino]-1-methylcyclohexyl glycinate hydrochloride or

trans-4-[(2,1,3-Benzoxadiazol-5-ylcarbonyl)(methyl)amino]cyclohexyl glycinate hydrochloride.

12. A compound according to claim 1 which is:

N-Cycloheptyl-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-(4,4-Dimethylcyclohexyl-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-Methyl-N-spiro[2.5]oct-6-yl-[2,1,3]-benzoxadiazole-5-carboxamide

N-Cyclobutyl-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-Cyclohexyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-Cyclopentyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-Cyclobutyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-(cis-4-Cyanocyclohexyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-D 3 -Methyl-N-tetrahydro-2H-pyran-4-yl-[2,1,3]-benzoxadiazole-5-carboxamide

N-(Tetrahydro-2H-pyran-4-yl)-[2,1,3]-benzoxadiazole-5-carboxamide

N-(Tetrahydro-2H-pyran-3-yl)-[2,1,3]-benzoxadiazole-5-carboxamide

N-Methyl-N-(tetrahydro-2H-pyran-3-yl)-[2,1,3]-benzoxadiazole-5-carboxamide

N-Ethyl-N-tetrahydro-2H-pyran-4-yl-[2,1,3]-benzoxadiazole-5-carboxamide

N-Cyclohexyl-N-ethyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-(Cyclohexylmethyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-Benzyl-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-Methyl-N-(tetrahydrofuran-2-ylmethyl)-[2,1,3]-benzoxadiazole-5-carboxamide

N-Methyl-N-pyridin-3-yl-[2,1,3]-benzoxadiazole-5-carboxamide

N-Methyl-N-phenyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-Cyclopropyl-N-tetrahydro-2H-pyran-4-yl-[2,1,3]-benzoxadiazole-5-carboxamide

N-Tetrahydro-2H-pyran-4-yl-N-(2,2,2-trifluoroethyl)-[2,1,3]-benzoxadiazole-5-carboxamide tert-Butyl-4-[([2,1,3]-benzoxadiazol-5-ylcarbonyl)(methyl)amino]piperidine-1-carboxylate

N-Methyl-N-piperidin-4-yl-[2,1,3]-benzoxadiazole-5-carboxamide hydrochloride

N-Methyl-N-(1-methylpiperidin-4-yl)-[2,1,3]-benzoxadiazole-5-carboxamide

N-(1-Acetylpiperidin-4-yl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-(1-Formylpiperidin-4-yl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-Methyl-N-[1-(methylsulfonyl]piperidin-4-yl)-[2,1,3]-benzoxadiazole-5-carboxamide

N-Methyl-N-(tetrahydro-2H-pyran-4-yl)-[2,1,3]-benzothiadiazole-5-carboxamide

N-Methyl-N-(tetrahydro-2H-thiopyran-4-yl)-[2,1,3]-benzoxadiazole-5-carboxamide

N-Methyl-N-(1-oxidotetrahydro-2H-thiopyran-4-yl)-[2,1,3]-benzoxadiazole-5-carboxamide N-Methyl-N-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-[2,1,3]-benzoxadiazole-5-carboxamide

N-Methyl-N-tetrahydro-2H-pyran-4-ylquinoxaline-6-carboxamide

N-[4-(Hydroxyimino)cyclohexyl]-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-[4-(Methoxyimino)cyclohexyl]-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-(4,4-Difluorocyclohexyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-(4-fluorocyclohex-3-en-1-yl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-(4-trans-Hydroxycyclohexyl)-[2,1,3]-benzoxadiazole-5-carboxamide

N-(trans-4-Hydroxy-4-methylcyclohexyl)-[2,1,3]-benzoxadiazole-5-carboxamide

N-(cis-4-Hydroxy-4-methylcyclohexyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-(cis-4-Hydroxy-4-ethylcyclohexyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-(trans-4-Hydroxy-4-ethylcyclohexyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-(cis-4-Ethynyl-4-hydroxycyclohexyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-(cis-4-But-3-en-1-yl-4-hydroxycyclohexyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-(trans-4-But-3-en-1-yl-4-hydroxycyclohexyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-(4-trans-Hydroxycyclohexyl)-N-D 3 -methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-(trans-4-Methoxycyclohexyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-(trans-4-Methoxycyclohexyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carbothioamide

N-(4-cis-Hydroxycyclohexyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-Methyl-N-[trans-4-(2H-tetrazol-2-yl)cyclohexyl]-[2,1,3]-benzoxadiazole-5-carboxamide

N-(trans-4-Azidocyclohexyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-(trans-4-Aminocyclohexyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-(cis-3-Hydroxycyclohexyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-(trans-3-Hydroxycyclohexyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-Methyl-N-(3-oxocyclohexyl)-[2,1,3]-benzoxadiazole-5-carboxamide

N-Methyl-N-(3,3-difluorocyclohexyl)-[2,1,3]-benzoxadiazole-5-carboxamide

N-(2-Hydroxycyclohexyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-Methyl-N-(2-oxocyclohexyl)-[2,1,3]-benzoxadiazole-5-carboxamide

N-Methyl-N-(2,2-difluorocyclohexyl)-[2,1,3]-benzoxadiazole-5-carboxamide

N-(2-Hydroxytetrahydro-2H-pyran-4-yl)-[2,1,3]-benzoxadiazole-5-carboxamide

N-(2-oxotetrahydro-2H-pyran-4-yl)-[2,1,3]-benzoxadiazole-5-carboxamide

N-Methyl-N-(2-oxotetrahydro-2H-pyran-4-yl)-[2,1,3]-benzoxadiazole-5-carboxamide

N-(2-Hydroxytetrahydro-2H-pyran-4-yl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide

N—(R)-Tetrahydrofuran-3-yl-[2,1,3]-benzoxadiazole-5-carboxamide

N-Methyl-N—(R)-tetrahydrofuran-3-yl-[2,1,3]-benzoxadiazole-5-carboxamide

N-2-(4-Morpholinyl)ethyl-[2,1,3]-benzoxadiazole-5-carboxamide

N-Methyl-N-2-(4-morpholinyl)ethyl-[2,1,3]-benzoxadiazole-5-carboxamide hydrochloride

N-Methyl-N-tetrahydro-2H-pyran-4-yl-[2,1,3]-benzoxadiazole-5-carbothioamide or

N-Methyl-N-tetrahydro-2H-pyran-4-ylmethyl-[2,1,3]-benzoxadiazole-5-carboxamide.

13. A pharmaceutical composition comprising an effective amount of a compound according to any of claims 1 - 12 in combination with a pharmaceutically acceptable carrier, additive or excipient.

14. The composition according to claim 13 wherein said compound comprises about 0.5% to about 75% by weight of said composition and said carrier, additive or excipient comprises about 25% to about 95.5% of said composition.

15. The compound according to claim 10 which is N-Cyclohexyl-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide.

16. The compound according to claim 10 which is N-Cyclopentyl-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide.

17. The compound according to claim 10 which is N-(trans-4-Cyanocyclohexyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide.

18. The compound according to claim 10 which is N-Methyl-N-tetrahydro-2H-pyran-4-yl-[2,1,3]-benzoxadiazole-5-carboxamide.

19. The compound according to claim 10 which is N-Methyl-N-(4-oxocyclohexyl)-[2,1,3]-benzoxadiazole-5-carboxamide.

20. The compound according to claim 10 which is N-(trans-4-Hydroxy-4-methylcyclohexyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide.

21. The compound according to claim 10 which is N-(4-trans-Hydroxycyclohexyl)-N-methyl-[2,1,3]-benzoxadiazole-5-carboxamide.

Assignments (8)
CHANGE OF NAME Recorded Feb 22, 2017
From: CORTEX PHARMACEUTICALS, INC.
To: RESPIRERX PHARMACEUTICALS INC
Reel/Frame 041777/0920 →
RELEASE OF LIEN Recorded Apr 15, 2015
From: COSUD
To: CORTEX PHARMACEUTICALS, INC.
Reel/Frame 035435/0594 →
LIEN Recorded Mar 20, 2013
From: COLEMAN SUDOL SAPONE, P.C.
To: CORTEX PHARMACEUTICALS, INC.
Reel/Frame 030054/0224 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 24, 2011
From: BIOVAIL LABORATORIES INTERNATIONAL INC.
To: CORTEX PHARMACEUTICALS INC.
Reel/Frame 026340/0914 →
PATENT SECURITY RELEASE AGREEMENT Recorded Mar 14, 2011
From: GOLDMAN SACHS LENDING PARTNERS LLC
To: BIOVAIL INTERNATIONAL LABORATORIES SRL; BIOVAIL INTERNATIONAL LABORATORIES (BARBADOS) SRL
Reel/Frame 025950/0073 →
SECURITY AGREEMENT Recorded Oct 4, 2010
From: BIOVAIL INTERNATIONAL LABORATORIES SRL; BIOVAIL INTERNATIONAL LABORATORIES (BARBADOS) SRL
To: GOLDMAN SACHS LENDING PARTNERS LLC, AS COLLATERAL AGENT
Reel/Frame 025084/0022 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 7, 2010
From: STREET, LESLIE; MUELLER, RUDOLF; LEE, STEVEN
To: CORTEX PHARMACEUTICALS, INC.
Reel/Frame 023756/0032 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 7, 2010
From: STREET, LESLIE; MUELLER, RUDOLF; LEE, STEVEN
To: CORTEX PHARMACEUTICALS, INC.
Reel/Frame 023756/0039 →