IP Library › Granted Patent US 12,473,266
Granted Patent B2
US 12,473,266 · App. 17/283,613 · Granted Nov 18, 2025

Benzoxazole and related compounds useful as chaperone-mediated autophagy modulators

Inventors: Ana Maria Cuervo (Bronx, NY); Evripidis Gavathiotis (Flushing, NY)
Assignee: ALBERT EINSTEIN COLLEGE OF MEDICINE
C07D263/57C07D413/12
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Quick Facts
Patent No.
US 12,473,266
App. No.
17/283,613
Granted
Nov 18, 2025
Kind
B2
Abstract

Compounds and pharmaceutically acceptable salts thereof of Formula I are disclosed. The variables, e.g. R 1 -R 9 , X, and Y are defined herein. Certain compounds and salts of Formula I are active as CMA modulators. The disclosure provides pharmaceutical compositions containing a compound of Formula I and methods of treating disorders responsive to CMA modulation.

Claims (59)

1 . A compound of the Formula I

or a pharmaceutically acceptable salt thereof, wherein

X is O;

Y is N;

(i) R 1 , R 3 , and R 4 are all hydrogen and R 2 is chloro; or

(ii) R 1 , R 2 , and R 4 are all hydrogen and R 3 is chloro;

R 5 , R 6 , R 8 , and R 9 are all hydrogen;

(a) R 7 is —NR 20 COR 21 , wherein R 20 is hydrogen, and R 21 is C 1 -C 2 haloalkyl when R 2 is chloro; and R 21 is C 2 haloalkyl when R 3 is chloro;

(b) R 7 is —NR 20 SO 2 R 21 , wherein R 20 is hydrogen, and R 21 is chosen from C 1 -C 2 haloalkyl and phenyl, which phenyl is optionally substituted with one or more halogens; or

(c) R 7 is a phenyl,

which is substituted with halogen, or one substituent —N(R 20 )COR 21 , wherein R 21 is chosen from C 1 -C 6 alkyl, and C 1 -C 2 haloalkyl.

2 . The compound or salt of claim 1 , wherein R 1 , R 3 , and R 4 are all hydrogen and R 2 is chloro.

3 . The compound or salt of claim 1 , wherein R 1 , R 2 , and R 4 are all hydrogen and R 3 is chloro.

4 . The compound or salt of claim 1 , where R 7 is —NR 20 COR 21 or —NR 20 SO 2 R 21 .

5 . A compound or salt of claim 1 , where

R 7 is —NR 20 COR 21 or NR 20 SO 2 R 21 ;

R 20 is hydrogen; and

R 21 is CF 3 .

6 . The compound or salt of claim 1 , where R 7 is a phenyl, which is substituted with halogen.

7 . The compound or salt of claim 1 , wherein

R 1 , R 3 , R 4 R 5 , R 6 , R 8 , and R 9 are hydrogen;

R 2 is chloro;

R 20 is hydrogen; and

R 21 is CF 3 .

8 . The compound or salt of claim 1 , where

Y is N and X is O;

R 1 , R 3 , R 4 R 5 , R 6 , R 8 , and R 9 are hydrogen;

R 2 is chloro; and

R 7 is phenyl, substituted with one or more halogen.

9 . The compound or salt of claim 1 , where

Y is N and X is O;

R 1 , R 3 , R 4 R 5 , R 6 , R 8 , and R 9 are hydrogen;

R 2 is chloro;

R 7 is phenyl substituted with one substituent —NR 20 COR 21 ;

R 20 is hydrogen; and

R 21 is chosen from C 1 -C 6 alkyl, or C 1 -C 2 haloalkyl.

10 . The compound or salt of claim 1 , where

Y is N and X is O;

R 1 , R 3 , R 4 R 5 , R 6 , R 8 , and R 9 are hydrogen;

R 2 is chloro;

R 7 is —NR 20 COR 21 or —NR 20 SO 2 R 21 ;

R 20 is hydrogen; and

R 21 is C 1 -C 2 haloalkyl.

11 . A compound or pharmaceutically acceptable salt thereof, wherein the compound is

N-(4-(6-chlorobenzo[d]oxazol-2-yl)phenyl)-2,2,2-trifluoroacetamide;

N-(4-(6-chlorobenzo[d]oxazol-2-yl)phenyl)-4-fluorobenzamide;

N-(4-(6-chlorobenzo[d]oxazol-2-yl)phenyl)-4-fluorobenzenesulfonamide;

N-(4-(6-chlorobenzo[d]oxazol-2-yl)phenyl)-1,1,1-trifluoromethanesulfonamide;

6-Chloro-2-(4′-fluoro-[1,1′-biphenyl]-4-yl)benzo[d]oxazole;

6-chloro-2-(4′-trifluoromethyl-[1,1′-biphenyl]-4-yl)benzo[d]oxazole;

N-(4′-(5-chlorobenzo[d]oxazol-2-yl)-[1,1′-biphenyl]-4-yl)-2,2,2-trifluoroacetamide; or

N-(4-(6-chlorobenzo[d]oxazol-2-yl)phenyl)-2,4-difluorobenzamide.

12 . The compound or salt thereof of claim 1 , wherein the compound is

13 . A pharmaceutical composition comprising a compound or salt of claim 1 together with a pharmaceutically acceptable carrier.

14 . A method of selectively activating chaperone-mediated autophagy in a subject in need thereof, comprising administering an effective amount of a compound or a pharmaceutically acceptable salt of claim 1 to the subject.

15 . The method of claim 14 , wherein the subject has Parkinson's disease, Huntington's disease, Alzheimer's disease, frontotemporal dementia, prion diseases, amyotrophic lateral sclerosis, retinal and macular degeneration, Leber congenital amaurosis, diabetes, acute liver failure, NASH, hepatosteatosis, alcoholic fatty liver, renal failure and chronic kidney disease, emphysema, sporadic inclusion body myositis, spinal cord injury, traumatic brain injury, a lysosomal storage disorder, a cardiovascular disease, or immunosenescence.

16 . A compound that is methyl 4-(6-chlorobenzo[d]oxazol-2-yl)benzoate.

17 . A method of selectively activating chaperone-mediated autophagy in a subject in need thereof, comprising administering an effective amount of a compound of claim 16 to the subject.

18 . The method of claim 17 , wherein the subject has Parkinson's disease, Huntington's disease, Alzheimer's disease, frontotemporal dementia, prion diseases, amyotrophic lateral sclerosis, retinal and macular degeneration, Leber congenital amaurosis, diabetes, acute liver failure, NASH, hepatosteatosis, alcoholic fatty liver, renal failure and chronic kidney disease, emphysema, sporadic inclusion body myositis, spinal cord injury, traumatic brain injury, a lysosomal storage disorder, a cardiovascular disease, or immunosenescence.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 30, 2024
From: CUERVO, ANA MARIA; GAVATHIOTIS, EVRIPIDIS
To: ALBERT EINSTEIN COLLEGE OF MEDICINE
Reel/Frame 068448/0474 →
Continuity (2)
Provisional Application 62743920 · Oct 10, 2018
Related Publication 20210387953A1 · Dec 16, 2021
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