Compounds for targeting mutant huntingtin protein and uses thereof

Patent metadata

Field	Value
Publication number	US-12083108-B2
Application number	US-202217752683-A
Country	US
Kind code	B2
Filing date	May 24, 2022
Priority date	Feb 25, 2019
Publication date	Sep 10, 2024
Grant date	Sep 10, 2024

Abstract

The present disclosure relates generally to compounds that simultaneously bind both mutant huntingtin protein (mHTT) and an ubiquitin E3 ligase and their use as therapeutic agents, for example, in treating diseases, such as neurodegenerative disorders caused by aggregation of mHTT.

First claim

The invention claimed is:

1. A compound of formula (I):
W-L-ULM  (I)

or a pharmaceutically acceptable salt, a stereoisomer, a mixture of stereoisomers, or isotopically enriched analog thereof, wherein:
W is a compound of formula (B), formula (C), formula (D), formula (E), or formula (F):

wherein:
the point of attachment of W to L-ULM is at any substitutable atom of formula (B), or at any substitutable atom of formula (C), at any substitutable atom of formula (D), or at any substitutable atom of formula (E); and
the wavy line of formula (F) indicates the point of attachment of W to L of L-ULM;

Z 1 , Z 2 , Z 3 , and Z 4 are independently selected from CH and N, provided that at least two of Z 1 , Z 2 , Z 3 , and Z 4 are CH;
R 5 is heteroaryl, heterocycloalkenyl, or heterocycloalkyl, each of which is optionally substituted with one or two groups independently selected from cyano, halo, lower alkyl optionally substituted with amino, alkylamino, or di(alkyl)amino, lower alkoxy optionally substituted with lower alkoxy, optionally substituted amino, haloalkyl, di(alkyl)aminocarbonyl, alkylaminocarbonyl, and aminocarbonyl,
or

R 5 is phenyl optionally substituted with one or two groups independently selected from cyano, heteroaryl, halo, phenoxy, benzyloxy, heteroaryl, lower alkyl optionally substituted with amino, (alkyl)amino, or di(alkyl)amino, lower alkoxy, optionally substituted amino, di(alkyl)aminocarbonyl, alkylaminocarbonyl, and aminocarbonyl;
L 3 is —O— and L 4 is —(CR 8 R 9 ) p — or —(CR 8 R 9 ) p —O—; or
L 3 is —NR 10 — and L 4 is —C(O)— or —(R 8 R 9 ) p —; or
L 3 is —NR 10 — and L 4 is —C(O)(O)(R 8 R 9 ) p —; or
L 3 is —NR 10 — and L 4 is —C(O)(R 8 R 9 ) p (O)—; or
L 3 is —NR 10 — and L 4 is —C(O)(R 8 R 9 ) p —; or
L 3 is —NR 10 — and L 4 is —C(O)CR 8 ═CR 9 —; or
L 3 is —C(O)— and L 4 is NR 10 —; or
L 3 is —(R 8 R 9 ) p — and L 4 is —NR 10 —, —C(O)— or —O—; or
L 3 is absent and L 4 is absent; or
L 3 taken together with L 4 is —CH═CH—, —C≡C—, or heterocyclylene;
L 5 is —CH═CH—, or L 5 is absent;
R 6 is selected from heterocycloalkyl, aryl, and heteroaryl, each of which is optionally substituted with one or two groups selected from
—OC(O)—R 11 ,
—C(O)O—R 11 ,
amino,
halo,
haloalkyl,
phenyl,
heteroaryl,
cyano,
(lower alkyl)thio,
phenoxy,
phenoxymethyl,
heteroaryloxy,
heteroaryloxy substituted with lower alkyl,
hydroxyl,
lower alkenyloxy,
lower alkoxy,
lower alkoxy substituted with lower alkoxy, amino, (alkyl)amino, (dialkyl)amino, heterocycloalkyl, heteroaryl, or halo,
lower alkyl, and
lower alkyl substituted with amino, (alkyl)amino, (dialkyl)amino, hydroxyl or lower alkoxy;

X 1 is NR 12 , O, or S;
Y 1 is CR 12 or N;
R 10 is hydrogen or lower alkyl;
R 12 is hydrogen, halo, cyano, or lower alkyl;
each R 7 is independently selected from lower alkyl, lower alkoxy, and halo;
R 11 is lower alkyl;
each R 8 is independently selected from hydrogen, hydroxyl, trifluoromethyl, and lower alkyl;
each R 9 is independently selected from hydrogen and lower alkyl;
n is 0 or 1;
p is 0, 1, or 2;
X 2 is (CR 16 ═CR 16 ), O, NH, or S;
Y 2 is CR 16 or N;
each R 16 is independently selected from hydrogen, halo, cyano, and lower alkyl;
R 13 is aryl, heteroaryl, or heterocycloalkyl, each of which is optionally substituted with one or two groups independently selected from alkynyl, heteroaryl, cyano, optionally substituted amino, halo, and lower alkyl optionally substituted with optionally substituted amino;
L 6 is absent, C(O)O, O, or NR 17 ,
R 17 is hydrogen or lower alkyl;
L 7 is (CH 2 ) q ;
R 14 is hydrogen, hydroxyl, lower alkyl, lower haloalkyl, halo, or lower alkoxy,
each R 15 is independently selected from lower alkyl, lower alkoxy, and halo; or
R 14 and R 15 , taken together with any intervening atoms forms a 5- to 7-membered heterocycloalkyl ring;
z is 0 or 1;
q is 0, 1, or 2;
R 18 is aryl, heteroaryl, or heterocycloalkenyl, each of which is optionally substituted with one or two groups independently selected from alkynyl, heteroaryl, cyano, optionally substituted amino, halo, lower alkyl, and lower alkyl substituted with optionally substituted amino;
L 8 is O or NR 21 ;
R 21 is hydrogen or lower alkyl;
L 9 is (CH 2 ) x ;
R 19 is hydrogen, aryl, aryl substituted with hydroxyl or lower alkoxy, heteroaryl, and heteroaryl substituted with hydroxyl or lower alkoxy;
each R 20 is independently selected from lower alkyl, lower alkoxy, halo, and oxo (as a substituent on the heterocycloalkyl ring);
x is 0, 1, or 2;
y is 0 or 1;
J is C(═O) or —CH 2 —;
X 3 is S or N;
Y 3 is CH or N;
Z 5 is CH or N;
Q is N or S;
for each occurrence, R 23 is independently selected from halo, lower alkoxy, hydroxy, aryl, heteroaryl, cycloalkoxy, and lower alkyl, wherein the lower alkoxy, cycloalkoxy, lower alkyl, aryl, or heteroaryl are each optionally substituted with one, two, or three groups independently selected from lower alkoxy, alkenyl, —NR 24 R 25 , halo, and heteroaryl optionally substituted with one to three lower alkoxy;
R 21 is hydrogen or lower alkyl; and
R 22 is alkyl, aryl, aralkyl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, or heteroaralkyl, each of which is optionally substituted with one, two, or three groups independently selected from hydroxy, lower alkoxy optionally substituted with lower alkoxy or halo, lower alkyl optionally substituted with halo, halo, heteroaryl, —(CH 2 )NR 24 R 25 , oxo, cyano, and —C(O)—NR 24 R 25 , or
R 21 and R 22 taken together with the nitrogen to which they are bound form a heterocycloalkyl ring, optionally substituted with one, two, or three groups independently selected from hydroxy, lower alkoxy, lower alkyl, halo, and —C(O)—NR 24 R 25 ;
t is 0, 1, or 2;
each R 24 is independently selected from hydrogen and lower alkyl;
each R 25 is independently selected from hydrogen and lower alkyl; or
R 24 and R 25 taken together with the nitrogen to which they are bound form a heterocycloalkyl ring, optionally substituted with one, two, or three groups independently selected from hydroxy, lower alkoxy, lower alkyl, halo, and —C(O)—NR 26 R 27 ;
each R 26 is independently hydrogen or lower alkyl;
each R 27 is independently hydrogen or lower alkyl;
s is 0, 1, or 2;
r is 1 or 2;
R 28 is heteroaryl optionally substituted with one, two, or three groups independently selected from cyano, lower alkoxy, lower alkenyl, —NR 24 R 25 , halo, and heteroaryl optionally substituted with one to three lower alkoxy;

L is a bond or
-G 1 -((CH 2 ) a -G 2 ) c -(CH 2 ) b -G 3 -

wherein:
each of G 1 , G 2 , and G 3 are independently a bond, —NR 28 —, —O—, —S(O) 0-2 —, —NR 28 C(O)—, —C(O)NR 28 —, —NR 28 S(O) 2 —, —S(O) 2 NR 28 —, —CR 29 ═N—NR 28 —, —NR 28 —N═CR 29 —, or —C(O)—, alkylene, heteroalkylene, alkenylene, heteroalkenylene, alkynylene, heteroalkynylene, arylene, heteroarylene, cycloalkylene, or heterocycloalkylene; wherein each alkylene, heteroalkylene, alkenylene, heteroalkenylene, alkynylene, heteroalkynylene, arylene, heteroarylene, cycloalkylene or heterocycloalkylene is independently optionally substituted with one to five substituents independently selected from oxo, halo, C 1-4 alkyl, C 1-4 alkoxy, and C 1-4 haloalkyl;
each R 28 is independ

Assignees

• Chdi Foundation Inc

Inventors

• Dominguez Celia
• Bard Jonathan
• Lee Matthew R
• Liu Longbin
• Prime Michael Edward
• Coe Samuel

Classifications

• A61K31/427

  not condensed and containing further heterocyclic rings · CPC title

• A61K31/165

  having aromatic rings, e.g. colchicine, atenolol, progabide · CPC title

• A61K47/555

  pre-targeting systems involving an organic compound, other than a peptide, protein or antibody, for targeting specific cells · CPC title

• A61P25/00

  Drugs for disorders of the nervous system · CPC title

• C07D401/12

  linked by a chain containing hetero atoms as chain links · CPC title