IP Library Granted Patent US 10,188,651
Granted Patent B2
US 10,188,651 · App. 15/195,699 · Granted Jan 29, 2019

Methods of treating sleep disorders

Inventors: John Ciallella (Exton, PA); John Gruner (Exton, PA); Andrew G. Reaume (Exton, PA); Michael S. Saporito (Exton, PA)
Assignee: Melior Pharmaceuticals II, LLC
A61K31/506A61K9/0053A61K31/198A61K31/4245A61K31/4439A61K31/501C07D271/04C07D413/12Y02A50/465
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Quick Facts
Patent No.
US 10,188,651
App. No.
15/195,699
Granted
Jan 29, 2019
Kind
B2
Abstract

The present disclosure describes compounds and pharmaceutically acceptable salts thereof and compositions and formulations comprising the same that are useful in methods of treating dyskinesia or related disorders, and methods for treating dyskinesia or related disorders.

Claims (23)

1. A method of treating a sleep disorder associated with altered sleep rhythm and/or architecture in a mammal comprising administering to the mammal in need thereof an effective amount of a compound of Formula Ia-1, Formula Ia-2, Formula Ib-1, Formula Ib-2, Formula Ic-1, Formula Ic-2, Formula Id-1, or Formula Id-2:

or a pharmaceutically acceptable salt thereof, wherein the sleep disorder associated with altered sleep rhythm and/or architecture is insomnia, restless legs syndrome, narcolepsy, REM sleep behavior disorder, or disrupted circadian rhythm associated with sleep apnia, shift work, or jet lag; wherein:

U is C;

each R 1 is, independently, H, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 1 -C 6 alkoxy, C 1 -C 6 alkylthio, —CN, —OH, —SH, halo, haloalkyl, —NO 2 , —N(═O) 2 , —C(═O)OH, —NH 2 , —CF 3 , —NH(C 1 -C 6 alkyl), —N(C 1 -C 6 alkyl) 2 , —C(═O)H, carbalkoxy, carboxamido, alkylsulfonyl, alkylsulfonyloxy, aminosulfinyl, dialkylaminosulfinyl, monoalkylaminosulfinyl, aminosulfonyl, monoalkylaminosulfonyl, dialkylaminosulfonyl, alkylsulfonylamino, hydroxysulfonyloxy, alkoxysulfonyloxy, alkylsulfonyloxy, hydroxysulfonyl, alkoxysulfonyl, alkylsulfonylalkyl, aminosulfonylalkyl, monoalkylaminosulfonylalkyl, dialkylaminosulfonylalkyl, aminosulfinylalkyl, monoalkylaminosulfinylalkyl, or dialkylaminosulfinylalkyl, where r is 0, 1, 2, 3, 4, or 5;

each R 2 and R 3 is, independently, H, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 1 -C 6 alkoxy, C 1 -C 6 alkylthio, —CN, —OH, —SH, halo, haloalkyl, —NO 2 , —C(═O)OH, —NH 2 , —CF 3 , —NH(C 1 -C 6 alkyl), —N(C 1 -C 6 alkyl) 2 , —C(═O)H, carbalkoxy, carboxamido, alkylsulfonyl, alkylsulfonyloxy, aminosulfinyl, dialkylaminosulfinyl, monoalkylaminosulfinyl, aminosulfonyl, monoalkylaminosulfonyl, dialkylaminosulfonyl, alkylsulfonylamino, hydroxysulfonyloxy, alkoxysulfonyloxy, alkylsulfonyloxy, hydroxysulfonyl, alkoxysulfonyl, alkylsulfonylalkyl, aminosulfonylalkyl, monoalkylaminosulfonylalkyl, dialkylaminosulfonylalkyl, aminosulfinylalkyl, monoalkylaminosulfinylalkyl, dialkylaminosulfinylalkyl, aryl, or arylC 1 -C 6 alkyl, where n is 0, 1, 2, 3, or 4;

each R 4 and R 5 is, independently, H, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 1 -C 6 alkoxy, C 1 -C 6 alkylthio, —CN, —OH, —SH, halo, haloalkyl, —NO 2 , —C(═O)OH, —NH 2 , —CF 3 , —NH(C 1 -C 6 alkyl), —N(C 1 -C 6 alkyl) 2 , —C(═O)H, carbalkoxy, carboxamido, alkylsulfonyl, alkylsulfonyloxy, aminosulfinyl, dialkylaminosulfinyl, monoalkylaminosulfinyl, aminosulfonyl, monoalkylaminosulfonyl, dialkylaminosulfonyl, alkylsulfonylamino, hydroxysulfonyloxy, alkoxysulfonyloxy, alkylsulfonyloxy, hydroxysulfonyl, alkoxysulfonyl, alkylsulfonylalkyl, aminosulfonylalkyl, monoalkylaminosulfonylalkyl, dialkylaminosulfonylalkyl, aminosulfinylalkyl, monoalkylaminosulfinylalkyl, dialkylaminosulfinylalkyl, aryl, or arylC 1 -C 6 alkyl, where p is 0, 1, 2, 3, or 4;

W is H or C 1 -C 6 alkyl;

Y is H, C 1 -C 6 alkoxy, C 1 -C 6 alkylthio, —CN, —OH, —SH, halo, haloalkyl, —NO 2 , —C(═O)OH, —NH 2 , —CF 3 , —NH(C 1 -C 6 alkyl), —N(C 1 -C 6 alkyl) 2 , —C(═O)H, carbalkoxy, carboxamido, alkylsulfonyl, alkylsulfonyloxy, aminosulfinyl, dialkylaminosulfinyl, monoalkylaminosulfinyl, aminosulfonyl, monoalkylaminosulfonyl, dialkylaminosulfonyl, alkylsulfonylamino, hydroxysulfonyloxy, alkoxysulfonyloxy, alkylsulfonyloxy, hydroxysulfonyl, alkoxysulfonyl, alkylsulfonylalkyl, aminosulfonylalkyl, monoalkylaminosulfonylalkyl, dialkylaminosulfonylalkyl, aminosulfinylalkyl, monoalkylaminosulfinylalkyl, or dialkylamino sulfinylalkyl;

X is O or S;

Z is O or S;

R 7 is H or halo;

Q is H, C 1 -C 6 alkyl, aryl, C 1 -C 6 alkylaryl, C 3 -C 6 cycloalkyl, or heteroaryl, each of which is optionally substituted with —(R 6 ) t , where t is 0, 1, 2, 3, 4, or 5;

R 8 is H or C 1 -C 6 alkyl; and

each R 6 is, independently, H, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 1 -C 6 alkoxy, C 1 -C 6 alkylthio, —CN, —OH, —SH, halo, haloalkyl, —NO 2 , —N(═O) 2 , —C(═O)OH, —NH 2 , —CF 3 , —O—S(═O) 2 OH, —NH(C 1 -C 6 alkyl), —N(C 1 -C 6 alkyl) 2 , —C(═O)H, —C(═O) C 1 -C 6 alkyl, —C(═O) C 1 -C 6 alkoxy, carbalkoxy, carboxamido, alkylsulfonyl, alkylsulfonyloxy, aminosulfinyl, dialkylaminosulfinyl, monoalkylaminosulfinyl, aminosulfonyl, monoalkylaminosulfonyl, dialkylaminosulfonyl, alkylsulfonylamino, hydroxysulfonyloxy, alkoxysulfonyloxy, alkylsulfonyloxy, hydroxysulfonyl, alkoxysulfonyl, alkylsulfonylalkyl, aminosulfonylalkyl, monoalkylaminosulfonylalkyl, dialkylaminosulfonylalkyl, aminosulfinylalkyl, monoalkylaminosulfinylalkyl, or dialkylaminosulfinylalkyl; or pharmaceutically acceptable salt thereof.

2. The method of claim 1 wherein the mammal is a human.

3. The method of claim 1 wherein the administration is oral.

4. The method of claim 1 wherein the sleep disorder associated with altered sleep rhythm and/or architecture is insomnia.

5. The method of claim 1 wherein the sleep disorder associated with altered sleep rhythm and/or architecture is restless legs syndrome.

6. The method of claim 1 wherein the sleep disorder associated with altered sleep rhythm and/or architecture is narcolepsy.

7. The method of claim 1 wherein the sleep disorder associated with altered sleep rhythm and/or architecture is REM sleep behavior disorder.

8. The method of claim 1 wherein the sleep disorder associated with altered sleep rhythm and/or architecture is disrupted circadian rhythm associated with sleep apnia, shift work, or jet lag.

9. A method of treating a sleep disorder in a human comprising orally administering to the human in need thereof an effective amount of 3-(β-phenylisopropyl)-N-phenylcarbamoyl sydnonimine, or a pharmaceutically acceptable salt thereof, wherein the sleep disorder is insomnia, restless legs syndrome, narcolepsy, REM sleep behavior disorder, or disrupted circadian rhythm associated with sleep apnia, shift work, or jet lag.

10. A method of treating a sleep disorder in a human comprising orally administering to the human in need thereof an effective amount of 3-(β-phenylisopropyl)-N-phenylcarbamoyl sydnonimine, or a pharmaceutically acceptable salt thereof, wherein the sleep disorder is insomnia, narcolepsy, REM sleep behavior disorder, or disrupted circadian rhythm associated with sleep apnia, shift work, or jet lag.

Assignments (3)
SECURITY INTEREST Recorded Nov 23, 2021
From: ADHERA THERAPEUTICS, INC.
To: CAVALRY FUND I LP
Reel/Frame 058312/0195 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 1, 2016
From: CIALLELLA, JOHN; GRUNER, JOHN; REAUME, ANDREW G.; SAPORITO, MICHAEL S.
To: MELIOR DISCOVERY, INC.
Reel/Frame 040187/0296 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 1, 2016
From: MELIOR DISCOVERY, INC.
To: MELIOR PHARMACEUTICALS II, LLC
Reel/Frame 040187/0429 →
Continuity (5)
Division 14702242 · May 1, 2015
Continuation 14472794 · Aug 29, 2014
Continuation PCTUS2014029827 · Mar 14, 2014
Provisional Application 61786714 · Mar 15, 2013
Related Publication 20170042894A1 · Feb 16, 2017