Dopamine d2 receptor ligands

a technology ligand, which is applied in the field of ligands of dopamine d2 receptor, can solve the problems of undesirable side effects and lack of clinical drug candidates that offer highly functionalized, and achieve the effects of minimizing potential associated side effects, minimizing potential undesirable side effects, and more selectivity and functionality

Active Publication Date: 2019-11-14
THE BROAD INST INC +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0010]The present invention relates to novel compounds that modulate dopamine D2 receptors. In particular, compounds of the present invention show functional selectivity at the dopamine D2 receptors and exhibit selectivity downstream of the D2 receptors, on the β-arrestin pathway and / or on the cAMP pathway. Compounds of the present invention exhibit different activity profiles either as agonist, antagonist, inverse agonist, or partial agonist. As these compounds are functionally selective downstream of the D2 receptors, they offer more selectivity and functionality in treatment of diseases or disorders in which dopamine plays a role, such as central nervous system disorders associated with D2 receptors, while minimizing potential associated side effects. Use of β-arrestin biased D2 receptor antagonists which selectively antagonize the β-arrestin pathway may offer a means to treat psychotic disorders while also minimizing potential undesirable side-effects associated with D2 receptor activity. Similarly, biased D2 receptor agonists which selectively activate either the β-arrestin pathway or the cAMP pathway may also be advantageous in treatment of disorders associated with dopamine receptors, such as Parkinson's disease, ADHD and restless leg syndrome or an endocrine disorder, e.g., galactorrhea, with fewer side-effects.
[0017]The present invention also provides a method of treating or preventing a disease or disorder in which modulation of D2 receptors (e.g., β-arrestin or Gi / cAMP) plays a role by administering to a subject in need thereof, a therapeutically effective amount of a selective β-arrestin antagonist, or a pharmaceutically acceptable salt, stereoisomer, racemate, tautomer, polymorph, hydrate, or solvate thereof, in combination with a pharmaceutically acceptable excipient or carrier, such that the disease or disorder is treated or prevented.
[0018]The present invention also provides a method of treating or preventing a disease or disorder in which modulation of D2 receptors (e.g., β-arrestin or Gi / cAMP) plays a role by administering to a subject in need thereof, a therapeutically effective amount of a compound which is a β-arrestin antagonist and a cAMP agonist, or a pharmaceutically acceptable salt, stereoisomer, racemate, tautomer, polymorph, hydrate, or solvate thereof, in combination with a pharmaceutically acceptable excipient or carrier, such that the disease or disorder is treated or prevented.
[0019]The present invention also provides a method of treating or preventing a disease or disorder in which modulation of D2 receptors (e.g., β-arrestin or Gi / cAMP) plays a role by administering to a subject in need thereof, a therapeutically effective amount of a compound of the invention, or a pharmaceutically acceptable salt, stereoisomer, racemate, tautomer, polymorph, hydrate, or solvate thereof, in combination with a pharmaceutically acceptable excipient or carrier, such that the disease or disorder is treated or prevented.

Problems solved by technology

There remains a lack of clinical drug candidates that offer highly functionalized targeting of dopamine D2 receptors that improve the clinical efficacy of antipsychotics, while at the same time limiting the undesirable side effects associated with D2-dopaminergic activity.

Method used

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  • Dopamine d2 receptor ligands
  • Dopamine d2 receptor ligands
  • Dopamine d2 receptor ligands

Examples

Experimental program
Comparison scheme
Effect test

examples

Synthesis of Intermediate I

[0561]

Step 1: (4-Chlorophenyl)(pyridin-2-yl)methanol

[0562]

[0563]To a stirred suspension of magnesium (5.37 g, 223.75 mmol, 3 equiv) in dry THF (60 mL) under argon atmosphere was added iodine (2 crystals), 1,2-dibromo ethane (2 drops). 1-bromo-4-chlorobenzene (25.76 g, 134.39 mmol, 1.8 equiv) was then added dropwise for 1 h at room temperature. The reaction mixture was stirred at room temperature for 1 h. A solution of picolinaldehyde (8 g, 74.68 mmol) in dry THF (19 mL) was added drop wise at room temperature and stirred for 2 h. After completion of reaction, the reaction mixture was quenched with saturated ammonium chloride solution and extracted with EtOAc. The combined organic extract was washed with water, brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. Purification using silica gel column chromatography (40% EtOAc / hexanes as eluent) afforded 12.26 g of (4-chlorophenyl) (pyridin-2-yl) methanol (yield=75%). ESI+MS: m / ...

example-1

1-(2-(3-chlorophenoxy)ethyl)-N-((4-chlorophenyl)(pyridin-2-yl)methyl)piperidine-4-carboxamide (I)

[0701]

[0702]To a stirred solution of N-((4-chlorophenyl)(pyridin-2-yl)methyl)piperidine-4-carboxamide (Int-I) (0.20 g, 0.60 mmol) in CH3CN (5 mL) were added potassium carbonate (0.251 g, 1.81 mmol, 3 equiv) and 1-(2-bromoethoxy)-3-chlorobenzene (0.143 g, 0.60 mmol, 1 equiv) at room temperature. The reaction mixture was heated at 80° C. and stirred for 6 h. After completion, the reaction mixture was diluted with water and extracted with CH2Cl2. The combined organic extract was dried over sodium sulfate, filtered and concentrated under reduced pressure. Purification using silica gel column chromatography (3% MeOH / CH2Cl2 as eluent) afforded 0.05 g of 1-(2-(3-chlorophenoxy) ethyl)-N-((4-chlorophenyl) (pyridin-2-yl) methyl) piperidine-4-carboxamide (Yield=17%).

[0703]1H NMR (400 MHz, DMSO-d6): δ 8.71(d, 1H, J=6.4 Hz), 8.51(d, 1H, J=4.0 Hz), 7.78-7.76 (m, 1H), 7.44 (d, 1H, J=8.0 Hz), 7.37-7.25 ...

example-2

1-(2-(4-chlorophenoxy)ethyl)-N-((4-chlorophenyl)(pyridine-2-yl)methyl) piperidine-4-carboxamide (2)

[0704]

[0705]Title compound was prepared from N-((4-chlorophenyl) (pyridin-2-yl) methyl) piperidine-4-carboxamide (Int-I) (0.20 g, 0.60 mmol) using the general methodology of Example-1. The product was washed with n-pentane and ether and afforded 0.1 g of 1-(2-(4-chlorophenoxy) ethyl)-N-((4-chlorophenyl) (pyridine-2-yl) methyl) piperidine-4-carboxamide (Yield=34%).

[0706]1H NMR (400 MHz, DMSO-d6): δ 8.70 (d, 1H, J=8.0 Hz), 8.51 (d, 1H, J=4.0 Hz), 7.80-7.75 (m, 1H), 7.44 (d, 1H, J=8.0 Hz), 7.37-7.35 (m, 7H), 6.96 (d, 2H, J=8.8 Hz), 6.13 (d, 1H, J=8.4 Hz), 4.05 (bs, 2H), 2.92 (bs, 2H), 2.65 (bs, 2H), 2.33-2.32 (m, 1H), 2.01 (bs, 2H), 1.66-1.55 (m, 4H); ESI+MS: m / z: 484.5 ([M+H]+).

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Abstract

The present invention relates to novel dopamine D2 receptor ligands. The invention further relates to functionally-biased dopamine D2 receptor ligands and the use of these compounds for treating or preventing central nervous system and systemic disorders associated with dysregulation of dopaminergic activity.

Description

RELATED APPLICATIONS[0001]The present application claims priority under 35 U.S.C. § 119(e) to U.S. provisional patent application, U.S. Ser. No. 62 / 094,510, filed Dec. 19, 2014, which is incorporated herein by reference.FIELD OF THE INVENTION[0002]The present invention relates to novel ligands of dopamine D2 receptors, in particular, functionally selective ligands of dopamine D2 receptors. The invention also relates to the use of these compounds in treating or preventing central nervous system disorders as well as systemic disorders associated with dopamine D2 receptors.BACKGROUND OF THE INVENTION[0003]G-protein-coupled receptors (GPCRs), also known as 7-transmembrane receptors, are the single largest class of drug targets, with more than 800 members in the human genome (Lefkowitz, Trends in Pharmacological Sciences (2004), 413). Dopamine receptors represent prototypic examples of GPCRs that mediate neurotransmission (Mis sale et al., Physiological Reviews (1998), 189). Dopamine is ...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C07D211/26A61P25/00C07D211/62C07D401/12C07D401/14C07D405/14C07D413/12C07D471/04C07D471/10
CPCC07D211/26A61P25/00C07D211/62C07D401/12C07D471/10C07D405/14C07D413/12C07D471/04C07D401/14
Inventor HOLSON, EDWARDWAGNER, FLORENCE FEVRIERWEIWER, MICHELSCOLNICK, EDWARDPALMER, MICHELLELEWIS, MICHAEL C.PAN, JENNIFER Q.ZHANG, YAN-LINGXU, QIHONG
Owner THE BROAD INST INC
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