Back to results
US 2020/0369650 A1Published application
Antagonists of the muscarinic acetylcholine receptor m4
AssigneeVanderbilt University
InventorsCraig W. Lindsley, P. Jeffrey Conn, Darren W. Engers, Julie L. Engers, Aaron M. Bender
Life of this patent
Estimating the term…
Abstract
Disclosed herein are 3-azabicyclo[3.1.0]hexan-6-amine compounds, which may be useful as antagonists of the muscarinic acetylcholine receptor M4 (mAChR M4). Also disclosed herein are methods of making the compounds, pharmaceutical compositions comprising the compounds, and methods of treating disorders using the compounds and compositions.
Claims18
A compound of formula (Ic), or a pharmaceutically acceptable salt thereof,
- wherein
- the ring containing W, X, Y and Z is a 6-membered heteroaryl ring containing two or one nitrogen atoms and W, X, Y and Z are independently N or CH;
- R1 is a 5- to 10-membered aromatic ring system optionally containing 1-2 nitrogen atoms and optionally substituted with 1-3 substituents independently selected from the group consisting of halogen, C1-C4 alkyl, C1-C4 haloalkyl, —NHCORe, and C3-C6 cycloalkyl;
- Re is hydrogen or C1-C4 alkyl;
- R4 is C4-C6 alkyl or —(CRbRc)p—Y;
- each Rb is independently hydrogen or C1-C4 alkyl;
- each Rc is independently hydrogen or C1-C4 alkyl;
- p is 0, 1, 2, 3, or 4;
- and
- Y′ is C3-C10 cycloalkyl;
- C3-C8 cycloalkenyl;
- aryl;
- a 5- or 6-membered heteroaryl having 1, 2, or 3 heteroatoms independently selected from N, O, and S;
- or a 5-, 6-, or 7-membered heterocycle having 1, 2, or 3 heteroatoms independently selected from N, O, and S;
- wherein Y′ is unsubstituted or substituted with one or two substituents independently selected from halo and C1-C4 alkyl.
12 more elements
Dependencies are inferred from the claim text.