1,2,4-triazole derivatives as tankyrase inhibitors

US11926614B2 · kind B2 · utility

Assignees

• OSLO UNIVERSITETSSYKEHUS · NO
• Forschungsverbund Berlin e.V. · DE
• UNIVERSITY OF OULU · FI

Inventors

• Stefan Krauss · Eidsvoll verk, NO
• Marc Nazare · Idstein, DE
• Lari Lehtiö · Oulu, FI
• Jo Waaler · Oslo, NO
• Anita WEGERT · Aldenhoven, DE
• Ruben Gerardus George Leenders · Nijmegen, NL

Key dates

• Filing date: Jun 19, 2019
• Grant date: Mar 12, 2024
• Expiry date: May 5, 2041

Classification

• Technology area (CPC C): Chemistry; Metallurgy
• CPC primary: C07B2200/07
• WIPO field: Pharmaceuticals
• WIPO sector: Chemistry

Abstract

The present invention relates to compounds of formula (I), tautomers, stereoisomers, pharmaceutically acceptable salts and pro-drugs thereof, to processes for their preparation, to pharmaceutical compositions containing such compounds and to their use in therapy wherein a dashed line indicates an optional bond; X represents: a 5- or 6-membered, unsaturated heterocyclic group optionally substituted by one or more (e.g. 1, 2 or 3) substituents independently selected from halogen (i.e. F, Cl, Br, I), C1-6 alkyl (e.g. C1-3 alkyl), C1-6 haloalkyl (e.g. C1-3 haloalkyl), C1-6 alkoxy (e.g. C1-3 alkoxy), —CN, —NO2, —N(R)2, and —SO2R (where each R is independently H or C1-6 alkyl, e.g. H or C1-3 alkyl); a C3-5 cycloalkyl group optionally substituted by one or more (e.g. 1 or 2) substituents independently selected from C1-6 alkyl (preferably C1-3 alkyl), C1-6 haloalkyl (e.g. C1-3 haloalkyl), and C1-6 alkoxy (e.g. C1-3 alkoxy); or an aryl group optionally substituted by one or more (e.g. 1, 2 or 3) substituents independently selected from halogen (i.e. F, Cl, Br, I), C1-6 alkyl (e.g C1-3 alkyl), C1-6 haloalkyl (e.g. C1-3 haloalkyl), and C1-6 alkoxy (e.g. C1-3 alkoxy); Y represents: an aryl or …