IP Library Granted Patent US 10,118,902
Granted Patent B2
US 10,118,902 · App. 15/319,329 · Granted Nov 6, 2018

Small molecule agonists of neurotensin receptor 1

Inventors: Anthony B. Pinkerton (La Jolla, CA); Paul M. Hershberger (La Jolla, CA); Satyamaheshwar Peddibhotla (La Jolla, CA); Patrick R. Maloney (La Jolla, CA); Michael P. Hedrick (La Jolla, CA)
Assignee: SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE
C07D239/94C07D401/04C07D401/12C07D401/14C07D403/04C07D403/12C07D409/14C07D487/10
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Quick Facts
Patent No.
US 10,118,902
App. No.
15/319,329
Granted
Nov 6, 2018
Kind
B2
Abstract

Provided herein are small molecule neurotensin receptor agonists, compositions comprising the compounds, and methods of using the compounds and compositions comprising the compounds.

Claims (198)

1. A compound of Formula (I), or a pharmaceutically acceptable salt or solvate thereof:

wherein,

ring A is phenyl, C 3 -C 6 cycloalkyl, C 2 -C 6 heterocycloalkyl, or monocyclic heteroaryl;

A is CH or N;

R 1 is halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkyl, C 1 -C 4 haloalkoxy, —OH, or —N(R a ) 2 ; and R 3 is hydrogen, C 1 -C 4 alkyl, or C 1 -C 4 haloalkyl;

or

R 1 is hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkyl, C 1 -C 4 haloalkoxy, or —N(R a ) 2 ; and R 3 and R 9 are taken together with the intervening atoms to form an optionally substituted C 2 -C 6 heterocycloalkyl;

each R a is independently selected from the group consisting of hydrogen, C 1 -C 4 alkyl, —C(═O)R 11 , —C(═O)—O—R 11 , —S(═O) 2 R 11 , —C(═O)R 11 , or 2 R a taken together with the nitrogen to which they are attached form an optionally substituted C 2 -C 6 heterocycloalkyl;

L 1 is absent, C 1 -C 4 alkylene, C 1 -C 4 alkenylene, C 1 -C 4 alkynylene, or —N(R b )—;

R b is hydrogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, —C(═O)R 11 , —C(═O)—O—R 11 , —S(═O) 2 R 11 , or —C(═O)R 11 ;

R 2 is hydrogen, halogen, —CN, —OH, —NO 2 , optionally substituted C 1 -C 4 alkyl, optionally substituted C 1 -C 4 alkoxy, optionally substituted C 1 -C 4 haloalkyl, optionally substituted C 1 -C 4 haloalkoxy, optionally substituted C 3 -C 6 cycloalkyl, optionally substituted C 2 -C 6 heterocycloalkyl, optionally substituted phenyl, or optionally substituted 5- or 6-membered heteroaryl;

R 5 and R 6 are each independently selected from hydrogen, halogen, —OH, and C 1 -C 4 alkyl, or when on the same carbon, R 5 and R 6 are taken together form an oxo;

R 7 is hydrogen, halogen, —CN, —OH, —NO 2 , —N(R 12 )—R 13 , —C(═O)—N(R 12 )—R 13 , —NR 12 C(═O)R 11 , —C(═O)—O—R 11 , —O—C(═O)—R 11 , —SR 12 , —S(═O)R 11 , —S(═O) 2 R 11 , —N(R 12 )S(═O) 2 R 11 , —S(═O) 2 —N(R 12 )—R 13 , —C(═O)R 11 , optionally substituted C 1 -C 4 alkyl, optionally substituted C 1 -C 4 alkoxy, optionally substituted C 1 -C 4 haloalkyl, optionally substituted C 1 -C 4 haloalkoxy, optionally substituted C 3 -C 6 cycloalkyl, optionally substituted C 2 -C 6 heterocycloalkyl, optionally substituted phenyl, or optionally substituted 5- or 6-membered heteroaryl;

R 8 is hydrogen, —OH, C 1 -C 4 alkyl, C 1 -C 4 fluoroalkyl, C 1 -C 4 alkoxy, C 1 -C 4 fluoroalkoxy, or —N(R a ) 2 ;

R 9 is hydrogen, C 1 -C 4 alkyl, or C 1 -C 4 fluoroalkyl;

X is —O— or —N(R b )—;

R 10 is hydrogen, C 1 -C 4 alkyl, C 1 -C 4 fluoroalkyl, —C(═O)R 11 , —C(═O)—O—R 11 , —C(═O)N(R 12 )R 13 , —S(═O) 2 R 11 , or —C(═O)R 11 ;

each R 11 is independently selected from the group consisting of optionally substituted C 1 -C 4 alkyl, optionally substituted C 1 -C 4 fluoroalkyl, optionally substituted C 3- C 6 cycloalkyl, optionally substituted C 2 -C 6 heterocycloalkyl, optionally substituted phenyl, and optionally substituted 5- or 6-membered heteroaryl;

each of R 12 and R 13 is independently selected from the group consisting of hydrogen, optionally substituted C 1 -C 4 alkyl, optionally substituted C 1 -C 4 fluoroalkyl, optionally substituted C 3 -C 6 cycloalkyl, optionally substituted C 2 -C 6 heterocycloalkyl, optionally substituted phenyl, and optionally substituted 5- or 6-membered heteroaryl; or R 12 and R 13 , when on the same nitrogen atom, are taken together with the nitrogen atom to which they are attached to form an optionally substituted C 2 -C 6 heterocycloalkyl;

n is 1, 2 or 3; and

m is 1, 2, 3 or 4.

2. The compound of claim 1 , or a pharmaceutically acceptable salt or solvate thereof, wherein:

ring A is phenyl or C 3 -C 6 cycloalkyl.

3. The compound of claim 2 , or a pharmaceutically acceptable salt or solvate thereof, wherein the compound of Formula (I) has the following structure:

4. The compound of claim 3 , or a pharmaceutically acceptable salt or solvate thereof, wherein L 1 is absent and the compound of Formula (I) has the following structure of Formula (Ia):

5. The compound of claim 1 , or a pharmaceutically acceptable salt or solvate thereof, wherein:

ring A is monocyclic heteroaryl.

6. The compound of claim 4 , a pharmaceutically acceptable salt or solvate thereof, wherein:

R 1 is halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkyl, C 1 -C 4 haloalkoxy, or —N(R a ) 2 ; and

R 3 is hydrogen or C 1 -C 4 alkyl.

7. The compound of claim 4 , or a pharmaceutically acceptable salt or solvate thereof, wherein:

R 1 is hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkyl, C 1 -C 4 haloalkoxy, or —N(R a ) 2 ; and

R 3 and R 9 are taken together with the intervening atoms to form an optionally substituted C 2 -C 6 heterocycloalkyl.

8. The compound of claim 7 , or a pharmaceutically acceptable salt or solvate thereof, wherein the compound of Formula (I) has the following structure of Formula (Ib):

9. The compound of claim 8 , or a pharmaceutically acceptable salt or solvate thereof, wherein the compound of Formula (Ib) has one of the following structures:

10. The compound of claim 8 , or a pharmaceutically acceptable salt or solvate thereof, wherein:

A is CH;

R 7 is hydrogen, halogen, —CN, —OH, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkyl, or C 1 -C 4 haloalkoxy;

R 8 is C 1 -C 4 alkoxy or —N(R a ) 2 ;

R 10 is hydrogen or C 1 -C 4 alkyl;

m is 1 or 2; and

n is 1 or 2.

11. The compound of claim 8 , or a pharmaceutically acceptable salt or solvate thereof, wherein:

A is N;

R 7 is hydrogen, halogen, —CN, —OH, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkyl, or C 1 -C 4 haloalkoxy;

R 8 is C 1 -C 4 alkoxy or —N(R a ) 2 ;

R 10 is hydrogen or C 1 -C 4 alkyl;

m is 1 or 2; and

n is 1 or 2.

12. A compound of Formula (VI), or a pharmaceutically acceptable salt or solvate thereof:

wherein,

ring A is C 3 -C 6 cycloalkyl, C 2 -C 6 heterocycloalkyl, or monocyclic heteroaryl;

ring B is an optionally substituted hetereocycloalkyl, wherein if ring B is substituted then it is substituted with R 5 and R 6 ;

R 1 is hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkyl, C 1 -C 4 haloalkoxy, or —N(R a ) 2 ;

each R a is independently selected from the group consisting of hydrogen, C 1 -C 4 alkyl, —C(═O)R 11 , —C(═O)—O—R 11 , —S(═O) 2 R 11 , and —C(═O)R 11 , or 2 R a taken together with the nitrogen to which they are attached form an optionally substituted C 2 -C 6 heterocycloalkyl;

L 1 is absent, C 1 -C 4 alkylene, C 1 -C 4 alkenylene, C 1 -C 4 alkynylene, —O—, or —N(R b )—;

R b is hydrogen, C 1 -C 4 alkyl or C 1 -C 4 haloalkyl, —C(═O)R 1 , —C(═O)—O—R 11 , S(═O) 2 R 11 , or —C(═O)R 11 ;

R 2 is hydrogen, halogen, —CN, —OH, —NO 2 , optionally substituted C 1 -C 4 alkyl, optionally substituted C 1 -C 4 alkoxy, optionally substituted C 1 -C 4 haloalkyl, optionally substituted C 1 -C 4 haloalkoxy, optionally substituted C 3 -C 6 cycloalkyl, optionally substituted C 2 -C 6 heterocycloalkyl, optionally substituted phenyl, or optionally substituted 5- or 6-membered heteroaryl;

L 2 is absent or an optionally substituted C 1 -C 4 alkylene;

R 3 is hydrogen, C 1 -C 4 alkyl, or C 1 -C 4 haloalkyl;

R 4 is hydrogen, optionally substituted C 1 -C 4 alkyl, —C 1 -C 4 alkylene-C(═O)OR 11 , —C 1 -C 4 alkylene-OR 10 , or —C 1 -C 4 alkylene-N(R b )(R 10 );

R 10 is hydrogen, C 1 -C 4 alkyl, C 1 -C 4 fluoroalkyl, —C(═O)R 11 , —C(═O)—O—R 11 , —C(═O)N(R 12 )R 13 , S(═O) 2 R 11 , or —C(═O)R 11 ; or R 10 and R b are taken together with the N atom to which they are attached to form a C 2 -C 6 heterocycle;

or R 3 and R 4 taken together with the nitrogen to which they are attached form an optionally substituted C 2 -C 6 heterocycloalkyl;

R 5 and R 6 are each independently selected from hydrogen, halogen, —OH, and C 1 -C 4 alkyl, or when on the same carbon, R 5 and R 6 are taken together form an oxo;

R 7 is hydrogen, halogen, —CN, —OH, —NO 2 , —N(R 12 )—R 13 , —C(═O)—N(R 12 )—R 13 , —NR 12 C(═O)R 11 , —C(═O)—O—R 11 , —O—C(═O)—R 11 , —SR 12 , —S(═O)R 11 , —S(═O) 2 R 11 , —N(R 12 )S(═O) 2 R 11 , —S(═O) 2 —N(R 12 )—R 13 , —C(═O)R 11 , optionally substituted C 1 -C 4 alkyl, optionally substituted C 1 -C 4 alkoxy, optionally substituted C 1 -C 4 haloalkyl, optionally substituted C 1 -C 4 haloalkoxy, optionally substituted C 3 -C 6 cycloalkyl, optionally substituted C 2 -C 6 heterocycloalkyl, optionally substituted phenyl, or optionally substituted 5- or 6-membered heteroaryl;

R 8 is hydrogen, —OH, C 1 -C 4 alkyl, C 1 -C 4 fluoroalkyl, C 1 -C 4 alkoxy, C 1 -C 4 fluoroalkoxy, or —N(R a ) 2 ;

each R 11 is independently selected from the group consisting of optionally substituted C 1 -C 4 alkyl, optionally substituted C 1 -C 4 fluoroalkyl, optionally substituted C 3- C 6 cycloalkyl, optionally substituted C 2 -C 6 heterocycloalkyl, optionally substituted phenyl, and optionally substituted 5- or 6-membered heteroaryl;

each of R 12 and R 13 is independently selected from the group consisting of hydrogen, optionally substituted C 1 -C 4 alkyl, optionally substituted C 1 -C 4 fluoroalkyl, optionally substituted C 3 -C 6 cycloalkyl, optionally substituted C 2 -C 6 heterocycloalkyl, optionally substituted phenyl, and optionally substituted 5- or 6-membered heteroaryl; or R 12 and R 13 , when on the same nitrogen atom, are taken together with the nitrogen atom to which they are attached to form an optionally substituted C 2 -C 6 heterocycloalkyl;

n is 1, 2 or 3; and

m is 1, 2, 3 or 4.

13. The compound of claim 12 , or a pharmaceutically acceptable salt or solvate thereof, wherein:

ring A is monocyclic heteroaryl;

R 1 is hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, or —N(R a ) 2 ;

L 1 is absent;

L 2 is absent or —CH 2 —;

R 3 is hydrogen or C 1 -C 4 alkyl;

R 4 is C 1 -C 4 alkyl, —C 1 -C 4 alkylene-OR 10 , or —C 1 -C 4 alkylene-N(R b )(R 10 );

or R 3 and R 4 taken together with the nitrogen to which they are attached form an optionally substituted C 2 -C 5 heterocycloalkyl;

R 7 is hydrogen, halogen, —CN, —OH, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkyl, or C 1 -C 4 haloalkoxy; and

m is 1 or 2.

14. The compound of claim 12 , or a pharmaceutically acceptable salt or solvate thereof, wherein:

ring A is C 3 -C 6 cycloalkyl;

R 1 is hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, or —N(R a ) 2 ;

L 1 is absent;

L 2 is absent or —CH 2 —;

R 3 is hydrogen or C 1 -C 4 alkyl;

R 4 is C 1 -C 4 alkyl, —C 1 -C 4 alkylene-OR 10 , or —C 1 -C 4 alkylene-N(R b )(R 10 );

or R 3 and R 4 taken together with the nitrogen to which they are attached form an optionally substituted C 2 -C 5 heterocycloalkyl;

R 7 is hydrogen, halogen, —CN, —OH, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkyl, or C 1 -C 4 haloalkoxy; and

m is 1 or 2.

15. The compound of claim 12 , or a pharmaceutically acceptable salt or solvate thereof, wherein:

ring B is an N-containing optionally substituted monocyclic heterocycloalkyl.

16. The compound of claim 15 , or a pharmaceutically acceptable salt or solvate thereof, wherein:

ring B is

and

R 5 and R 6 are each independently selected from hydrogen, halogen, —OH, and C 1 -C 4 alkyl, or when on the same carbon, R 5 and R 6 are taken together form an oxo.

17. The compound of claim 12 , or a pharmaceutically acceptable salt or solvate thereof, wherein:

ring B is an N-containing optionally substituted bicyclic heterocycloalkyl or an N-containing optionally substituted tricyclic heterocycloalkyl.

18. The compound of claim 17 , or a pharmaceutically acceptable salt or solvate thereof, wherein:

ring B is

19. A compound that is:

2-({2-(1-Fluoro-cyclopropyl)-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-quinazolin-6-yl}-methyl-amino)-ethanol;

{2-(1-fluoro-cyclopropyl)-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-quinazolin-6-yl}-(2-methoxy-ethyl)-methyl-amine;

{2-(1-fluoro-cyclopropyl)-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-quinazolin-6-yl}-methyl-propyl-amine;

{4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-2-[1-(methyl-propyl-amino)-cyclopropyl]-quinazolin-6-yl})-methyl-propyl-amine;

2-{[4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-2-(1-methyl-cyclopropyl)-quinazolin-6-yl]-methyl-amino)}-ethanol;

N-[4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-2-(1-methyl-cyclopropyl)-quinazolin-6-yl]-N,N′,N′-trimethyl-ethane-1,2-diamine;

2-{[4-[4-(2-dimethylamino-phenyl)-piperidin-1-yl]-2-(1-methyl-cyclopropyl)-quinazolin-6-yl]-methyl-amino}-ethanol;

[4-[4-(2-dimethylamino-phenyl)-piperidin-1-yl]-2-(1-methyl-cyclopropyl)-quinazolin-6-yl]-(2-methoxy-ethyl)-methyl-amine;

N-[4-[4-(2-dimethylamino-phenyl)-piperidin-1-yl]-2-(1-methyl-cyclopropyl)-quinazolin-6-yl]-N,N′,N′-trimethyl-ethane-1,2-diamine;

2-{[4-[4-(2-azetidin-1-yl-phenyl)-piperidin-1-yl]-2-(1-methyl-cyclopropyl)-quinazolin-6-yl]-methyl-amino}-ethanol;

[4-[4-(2-azetidin-1-yl-phenyl)-piperidin-1-yl]-2-(1-methyl-cyclopropyl)-quinazolin-6-yl]-(2-methoxy-ethyl)-methyl-amine;

N-(2-methoxyethyl)-4-(4-(2-methoxyphenyl)piperidin-1-yl)-N-methyl-2-(1-methylcyclopropyl)quinazolin-6-amine;

2-{[4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-2-(1-trifluoromethyl-cyclopropyl)-quinazolin-6-yl]-methyl-amino}-ethanol;

2-{[4-[4-(2-dimethylamino-phenyl)-piperidin-1-yl]-2-(1-trifluoromethyl-cyclopropyl)-quinazolin-6-yl]-methyl-amino}-ethanol;

2-{[4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-2-(1-methyl-cyclopentyl)-quinazolin-6-yl]-methyl-amino)}-ethanol;

{[4-[4-(2-Dimethylamino-phenyl)-piperidin-1-yl]-2-(1-methyl-cyclopentyl)-quinazolin-6-yl]-methyl-amino}-ethanol;

2-{[4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-2-(1-trifluoromethyl-cyclopentyl)-quinazolin-6-yl]-methyl-amino}-ethanol;

2-{[4-[4-(2-dimethylamino-phenyl)-piperidin-1-yl]-2-(1-trifluoromethyl-cyclopentyl)-quinazolin-6-yl]-methyl-amino}-ethanol;

2-({2-(1-fluoro-cyclobutyl)-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-quinazolin-6-yl}-methyl-amino)-ethanol;

2-{[4-[4-(2-dimethylamino-phenyl)-piperidin-1-yl]-2-(1-fluoro-cyclobutyl)-quinazolin-6-yl]-methyl-amino}-ethanol;

2-{[4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-2-(1-trifluoromethyl-cyclobutyl)-quinazolin-6-yl]-methyl-amino}-ethanol;

2-{[4-[4-(2-Dimethylamino-phenyl)-piperidin-1-yl]-2-(1-trifluoromethyl-cyclobutyl)-quinazolin-6-yl]-methyl-amino}-ethanol;

2-{[4-[4-(2-dimethylamino-phenyl)-piperidin-1-yl]-2-(1-methyl-cyclobutyl)-quinazolin-6-yl]-methyl-amino}-ethanol;

2-{[4-[4-(2-Methoxy-phenyl)-piperidin-1-yl]-2-(1-methyl-cyclobutyl)-quinazolin-6-yl]-methyl-amino)}-ethanol;

2-({2-(1-fluoro-cyclopentyl)-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-quinazolin-6-yl}-methyl-amino)-ethanol;

2-{[4-[4-(2-dimethylamino-phenyl)-piperidin-1-yl]-2-(1-fluoro-cyclopentyl)-quinazolin-6-yl]-methyl-amino}-ethanol;

1-{2-cyclopropyl-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-quinazolin-6-yl}-piperidin-4-ol;

{2-cyclopropyl-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-6-(4-methoxy-piperidin-1-yl)-quinazoline;

(1-{2-cyclopropyl-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-quinazolin-6-yl})-piperidin-4-yl)-dimethyl-amine;

1-{2-cyclopropyl-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-quinazolin-6-yl}-pyrrolidin-3-ol;

2-cyclopropyl-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-6-(3-methoxy-pyrrolidin-1-yl)-quinazoline;

(R)-1-{2-cyclopropyl-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-quinazolin-6-yl}-pyrrolidin-3-ol;

(S)-1-(2-cyclopropyl-4-(4-(2-methoxyphenyl)piperidin-1-yl)quinazolin-6-yl)pyrrolidin-3-ol;

(R)-2-cyclopropyl-4-(4-(2-methoxyphenyl)piperidin-1-yl)-6-(3-methoxypyrrolidin-1-yl)quinazoline;

(S)-2-cyclopropyl-4-(4-(2-methoxyphenyl)piperidin-1-yl)-6-(3-methoxypyrrolidin-1-yl)quinazoline;

[(1-{2-cyclopropyl-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-quinazolin-6-yl}-piperidin-4-yl)-methyl-amino]-acetic acid ethyl ester;

4-(4-(2-methoxyphenyl)piperidin-1-yl)-N2,N2,N6-trimethyl-N6-propylquinazoline-2,6-diamine;

4-(4-(2-methoxyphenyl)piperidin-1-yl)-N2,N2-dimethyl-N6,N6-dipropylquinazoline-2,6-diamine;

N2-Cyclobutyl-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-N6-methyl-N6-propyl-quinazoline-2,6-diamine;

2-((2-(cyclobutylamino)-4-(4-(2-methoxyphenyl)piperidin-1-yl) quinazolin-6-yl)(methyl)amino)ethanol;

2-({2-cyclopropyl-4-[6-(2-methoxy-phenyl)-2,6-diaza-spiro [3.3]hept-2-yl]-quinazolin-6-yl}-methyl-amino)-ethanol;

2-((2-cyclopropyl-4-(4-(3-methoxythiophen-2-yl)piperidin-1-yl) quinazolin-6-yl)(methyl)amino)ethanol;

2-((4-(4-cyclohexylpiperidin-1-yl)-2-(1-fluorocyclopropyl) quinazolin-6-yl)(methyl)amino)ethanol;

2-(4-{2-cyclopropyl-6-[(2-hydroxy-ethyl)-methyl-amino]-quinazolin-4-yl}-piperazin-1-yl)-cyclopentanol;

2-{4-[2-cyclopropyl-6-(methyl-propyl-amino)-quinazolin-4-yl]-piperazin-1-yl}-cyclopentanol;

2-(4-{2-cyclopropyl-6-[methyl-(2-morpholin-4-yl-ethyl)-amino]-quinazolin-4-yl}-piperazin-1-yl)-cyclopentanol;

(1-Fluoro-cyclopropyl)-{7-fluoro-6-[(2-hydroxy-ethyl)-methyl-amino]-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-quinazolin-2-yl)}-methanone;

{7-Chloro-6-[(2-hydroxy-ethyl)-methyl-amino]-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-quinazolin-2-yl}-(1-fluoro-cyclopropyl)-methanone;

(S)-1-(2-cyclopropyl-4-(4-(2-methoxyphenyl)piperidin-1-yl)quinazolin-6-yl)pyrrolidin-3-ol;

(S)-2-cyclopropyl-4-(4-(2-methoxyphenyl)piperidin-1-yl)-6-(3-methoxypyrrolidin-1-yl)quinazoline;

(R)-1-{2-cyclopropyl-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-quinazolin-6-yl}-pyrrolidin-3-ol;

(R)-2-cyclopropyl-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-6-(3-methoxy-pyrrolidin-1-yl)-quinazoline;

(S)-1-{2-(1-Fluoro-cyclopropyl)-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-quinazolin-6-yl}-pyrrolidin-3-ol;

(R)-1-{2-(1-Fluoro-cyclopropyl)-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-quinazolin-6-yl}-pyrrolidin-3-ol;

2-((2-(1-fluorocyclopropyl)-4-(4-(2-methoxyphenyl)piperidin-1-yl)quinazolin-6-yl)(methyl)amino)acetic acid;

2-((8-chloro-2-(1-fluorocyclobutyl)-4-(4-(2-methoxyphenyl)piperidin-1-yl)quinazolin-6-yl)(methyl)amino)ethanol;

3-{8-Chloro-2-(1-fluoro-cyclobutyl)-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-quinazolin-6-yl)}-cyclopentanol;

3-{8-Chloro-2-(1-fluoro-cyclobutyl)-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-quinazolin-6-yl)}-cyclopentanol;

2-({2-Cyclopropyl-4-[4-(2-methoxy-cyclopentyl)-piperazin-1-yl]-quinazolin-6-yl)}-methyl-amino)-ethanol;

2-cyclopropyl-4-(4-(2-methoxycyclopentyl)piperazin-1-yl)-N-methyl-N-propylquinazolin-6-amine

2-{[4-(4-Cyclohexyl-piperidin-1-yl)-2-(1-fluoro-cyclopropyl)-quinazolin-6-yl]-methyl-amino}-ethanol

2-({2-(1-Fluoro-cyclopropyl)-4-[4-(2-methoxy-cyclohexyl)-piperidin-1-yl]-quinazolin-6-yl}-methyl-amino)-ethanol;

2-({2-Cyclopropyl-4-[4-(3-methoxy-thiophen-2-yl)-piperidin-1-yl]-quinazolin-6-yl}-methyl-amino)-ethanol;

2-({2-(1-Fluoro-cyclopropyl)-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-pyrido [3,4-d]pyrimidin-6-yl}-methyl-amino)-ethanol;

1-{2-(1-Fluoro-cyclopropyl)-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-pyrido[3,4-d]pyrimidin-6-yl}-pyrrolidin-3-ol;

1-{2-(1-Fluoro-cyclopropyl)-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-pyrido [3,4-d]pyrimidin-6-yl}-pyrrolidin-3-ol;

2-({2-(1-Fluoro-cyclobutyl)-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-pyrido[3,4-d]pyrimidin-6-yl}-methyl-amino)-ethanol;

1-{2-(1-Fluoro-cyclobutyl)-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-pyrido [3,4-d]pyrimidin-6-yl}-pyrrolidin-3-ol;

1-{2-(1-Fluoro-cyclobutyl)-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-pyrido [3,4-d]pyrimidin-6-yl}-pyrrolidin-3-ol;

2-({8-Chloro-2-(1-fluoro-cyclopropyl)-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-quinazolin-6-yl}-methyl-amino)-ethanol;

1-{8-Chloro-2-(1-fluoro-cyclopropyl)-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-quinazolin-6-yl}-pyrrolidin-3-ol;

1-{8-Chloro-2-(1-fluoro-cyclopropyl)-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-quinazolin-6-yl}-pyrrolidin-3-ol;

2-{[8-Fluoro-4-[4-(3-methoxy-pyrazin-2-yl)-piperidin-1-yl]-2-(1-methyl-cyclopropyl)-quinazolin-6-yl]-methyl-amino}-ethanol;

2-{[4-[4-(3-Methoxy-pyrazin-2-yl)-piperidin-1-yl]-2-(1-methyl-cyclopropyl)-quinazolin-6-yl]-methyl-amino}-ethanol;

2-{[2-(1-Fluoro-cyclopropyl)-4-(3-methoxy-3′,4′,5′,6′-tetrahydro-2′H-[2,4′]bipyridinyl-1′-yl)-quinazolin-6-yl]-methyl-amino}-ethanol;

2-{[2-(1-Fluoro-cyclopropyl)-4-(2-methoxy-3′,4′,5′,6′-tetrahydro-2′H-[3,4′]bipyridinyl-1′-yl)-quinazolin-6-yl]-methyl-amino}-ethanol;

2-({2-(1-Fluoro-cyclopropyl)-4-[4-(3-methoxy-pyrazin-2-yl)-piperidin-1-yl]-quinazolin-6-yl}-methyl-amino)-ethanol;

2-({2-(1-Fluoro-cyclopropyl)-4-[4-(3-methoxy-pyridin-2-yl)-piperazin-1-yl]-quinazolin-6-yl}-methyl-amino)-ethanol;

2-{[2-(1-Fluoro-cyclopropyl)-4-(4-methoxy-3′,4′,5′,6′-tetrahydro-2′H-[3,4′]bipyridinyl-1′-yl)-quinazolin-6-yl]-methyl-amino}-ethanol;

2-({2-(1-Fluoro-cyclopropyl)-4-[4-(5-methoxy-pyrimidin-4-yl)-piperidin-1-yl]-quinazolin-6-yl}-methyl-amino)-ethanol;

2-{[2-(1-Fluoro-cyclopropyl)-4-(3′-methoxy-3,4,5,6-tetrahydro-2H-[4,4′]bipyridinyl-1-yl)-quinazolin-6-yl]-methyl-amino}-ethanol;

2-({8-Fluoro-2-(1-fluoro-cyclopropyl)-4-[4-(3-methoxy-pyrazin-2-yl)-piperidin-1-yl]-quinazolin-6-yl}-methyl-amino)-ethanol;

2-{[8-Fluoro-2-(1-fluoro-cyclopropyl)-4-(2-methoxy-3′,4′,5′,6′-tetrahydro-2′H-[3,4′]bipyridinyl-1′-yl)-quinazolin-6-yl]-methyl-amino-}-ethanol;

2-({8-Fluoro-2-(1-fluoro-cyclopropyl)-4-[4-(3-methoxy-pyridin-2-yl)-piperazin-1-yl]-quinazolin-6-yl}-methyl-amino)-ethanol;

2-{[8-Fluoro-2-(1-fluoro-cyclopropyl)-4-(3-methoxy-3′,4′,5′,6′-tetrahydro-2′H-[2,4′]bipyridinyl-1′-yl)-quinazolin-6-yl]-methyl-amino}-ethanol;

2-({8-Fluoro-2-(1-fluoro-cyclopropyl)-4-[4-(5-methoxy-pyrimidin-4-yl)-piperidin-1-yl]-quinazolin-6-yl}-methyl-amino)-ethanol;

2-({2-(1-Fluoro-cyclopropyl)-4-[4-(4-iodo-2-methoxy-phenyl)-piperazin-1-yl]-quinazolin-6-yl}-methyl-amino)-ethanol;

2-({2-(1-Fluoromethyl-cyclopropyl)-4-[4-(3-methoxy-pyrazin-2-yl)-piperidin-1-yl]-quinazolin-6-yl}-methyl-amino)-ethanol;

2-({2-(1-Fluoro-cyclobutyl)-4-[4-(3-methoxy-pyrazin-2-yl)-piperidin-1-yl]-quinazolin-6-yl}-methyl-amino)-ethanol;

1-(6-((2-hydroxyethyl)(methyl)amino)-4-(4-(3-methoxypyrazin-2-yl)piperidin-1-yl)quinazolin-2-yl)cyclobutanol;

(2-(1-Fluoro-cyclopropyl)-4-{4-[2-(2-fluoro-ethoxy)-phenyl]-piperidin-1-yl)-quinazolin-6-yl)-[2-(2-fluoro-ethoxy)-ethyl]-methyl-amine;

{2-(1-Fluoro-cyclopropyl)-4-[4-(2-methoxy-phenyl)-piperidin-1-yl]-quinazolin-6-yl}-[2-(2-fluoro-ethoxy)-ethyl]-methyl-amine;

2-{1-[6-{[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-methyl-amino}-2-(1-fluoro-cyclopropyl)-quinazolin-4-yl]-piperidin-4-yl}-phenol;

2-[(2-(1-Fluoro-cyclopropyl)-4-{4-[2-(2-fluoro-ethoxy)-phenyl]-piperidin-1-yl}-quinazolin-6-yl)-methyl-amino]-ethanol;

or a pharmaceutically acceptable salt or solvate thereof.

20. A pharmaceutical composition comprising a compound of claim 1 , or a pharmaceutically acceptable salt or solvate thereof, and a pharmaceutically acceptable excipient.

21. A method of modulating neurotensin or neurotensin receptor 1 in a subject, comprising administering to the subject a compound of claim 1 , or a pharmaceutically acceptable salt or solvate thereof.

Assignments (2)
CHANGE OF NAME Recorded Sep 21, 2018
From: SANFORD-BURNHAM MEDICAL RESEARCH INSTITUTE
To: SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE
Reel/Frame 047129/0049 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 8, 2017
From: PINKERTON, ANTHONY B.; HERSHBERGER, PAUL M.; PEDDIBHOTLA, SATYAMAHESHWAR; MALONEY, PATRICK R.; HEDRICK, MICHAEL P.
To: SANFORD-BURNHAM MEDICAL RESEARCH INSTITUTE
Reel/Frame 041207/0751 →
Continuity (2)
Provisional Application 62017046 · Jun 25, 2014
Related Publication 20170240514A1 · Aug 24, 2017