ES2626801T3 - Compuestos de triazolopiridina como inhibidores de pde10a - Google Patents

Compuestos de triazolopiridina como inhibidores de pde10a Download PDF

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Publication number
ES2626801T3
ES2626801T3 ES12759445.5T ES12759445T ES2626801T3 ES 2626801 T3 ES2626801 T3 ES 2626801T3 ES 12759445 T ES12759445 T ES 12759445T ES 2626801 T3 ES2626801 T3 ES 2626801T3
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Prior art keywords
alkyl
halogen
heteroaryl
aryl
hydroxyl
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ES12759445.5T
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Inventor
Alexander Flohr
Katrin Groebke Zbinden
Matthias Koerner
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F Hoffmann La Roche AG
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F Hoffmann La Roche AG
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16—Anti-Parkinson drugs
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/22—Anxiolytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/24—Antidepressants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Abstract

Un compuesto de fórmula (I) **Fórmula** en la que R1 es arilo, heteroarilo o NR4R5, en el que dicho arilo y dicho heteroarilo pueden estar sustituidos con 1 a 3 sustituyentes seleccionados independientemente del grupo que consiste en hidroxilo, halógeno, alquilo C1-C7, alcoxi C1-C7 y haloalquilo C1-C7; R2 es hidrógeno, halógeno o alquilo C1-C7; R3 es arilo o heteroarilo, en el que dicho arilo y dicho heteroarilo pueden estar sustituidos con 1 a 3 sustituyentes seleccionados independientemente del grupo que consiste en alquilo C1-C7, hidroxilo, halógeno, -C(O)-NR6R7 y - C(O)-O-R8; R4 y R5 son independientemente alquilo C1-C7, cicloalquilo C3-C8, junto con el átomo de nitrógeno al que están unidos, forman un heterocicloalquilo que puede estar sustituido con 1 a 3 sustituyentes seleccionados independientemente del grupo que consiste en hidroxilo, halógeno, alquilo C1-C7, alcoxi C1-C7 y haloalquilo C1-C7; R6 y R7 son independientemente alquilo C1-C7, cicloalquilo C3-C8, junto con el átomo de nitrógeno al que están unidos, forman un heterocicloalquilo que puede estar sustituido con 1 a 3 sustituyentes seleccionados independientemente del grupo que consiste en hidroxilo, halógeno, alquilo C1-C7, alcoxi C1-C7 y haloalquilo C1-C7; R8 es hidrógeno, alquilo C1-C7, cicloalquilo; o una sal farmacéuticamente aceptable de los mismos.
ES12759445.5T 2011-09-19 2012-09-17 Compuestos de triazolopiridina como inhibidores de pde10a Active ES2626801T3 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP11181752 2011-09-19
EP11181752 2011-09-19
PCT/EP2012/068203 WO2013041472A1 (en) 2011-09-19 2012-09-17 Triazolopyridine compounds as pde10a inhibitors

Publications (1)

Publication Number Publication Date
ES2626801T3 true ES2626801T3 (es) 2017-07-26

Family

ID=46851999

Family Applications (1)

Application Number Title Priority Date Filing Date
ES12759445.5T Active ES2626801T3 (es) 2011-09-19 2012-09-17 Compuestos de triazolopiridina como inhibidores de pde10a

Country Status (18)

Country Link
US (2) US8946427B2 (es)
EP (1) EP2758396B1 (es)
JP (1) JP2014526533A (es)
KR (1) KR101584925B1 (es)
CN (1) CN103827114B (es)
AU (1) AU2012311713A1 (es)
BR (1) BR112014006248A2 (es)
CA (1) CA2846758C (es)
CL (1) CL2014000641A1 (es)
CO (1) CO6900144A2 (es)
EA (1) EA201490599A1 (es)
ES (1) ES2626801T3 (es)
IL (1) IL231403A0 (es)
MX (1) MX2014003025A (es)
PE (1) PE20141553A1 (es)
SG (1) SG11201400759RA (es)
UA (1) UA108711C2 (es)
WO (1) WO2013041472A1 (es)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013043520A1 (en) 2011-09-22 2013-03-28 Merck Sharp & Dohme Corp. Triazolopyridyl compounds as aldosterone synthase inhibitors
WO2013043518A1 (en) 2011-09-22 2013-03-28 Merck Sharp & Dohme Corp. Imidazopyridyl compounds as aldosterone synthase inhibitors
MY169128A (en) * 2013-04-30 2019-02-18 Hoffmann La Roche Pd-catalyzed coupling of pyrazole amides
TWI652014B (zh) 2013-09-13 2019-03-01 美商艾佛艾姆希公司 雜環取代之雙環唑殺蟲劑
JP6568855B2 (ja) 2014-07-30 2019-08-28 持田製薬株式会社 ピラゾール誘導体の製造方法
CN107074844A (zh) * 2014-07-30 2017-08-18 持田制药株式会社 吡唑衍生物的制造方法
CN107635984B (zh) 2015-03-11 2021-04-13 Fmc公司 杂环取代的二环唑杀有害生物剂
CN107743486B (zh) 2015-03-12 2021-04-09 Fmc公司 杂环取代的二环唑杀有害生物剂
US10800794B2 (en) 2015-10-08 2020-10-13 Fmc Corporation Heterocycle-substituted bicyclic azole pesticides
KR102600330B1 (ko) * 2017-08-22 2023-11-10 바이엘 악티엔게젤샤프트 해충 방제제로서의 헤테로시클렌 유도체
JP7253049B2 (ja) 2019-05-27 2023-04-05 日本農薬株式会社 架橋部に窒素原子を有する縮合複素環化合物又はその塩類及び該化合物を含有する農園芸用殺虫剤並びにその使用方法
AR119140A1 (es) 2019-06-13 2021-11-24 Pi Industries Ltd Compuestos heterocíclicos fusionados y su uso como agentes de control de plagas
CN110396157B (zh) * 2019-08-07 2021-07-30 广州市建筑科学研究院有限公司 缓释型聚羧酸纳米减水剂及其制备方法和应用

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6355653B1 (en) * 1999-09-06 2002-03-12 Hoffmann-La Roche Inc. Amino-triazolopyridine derivatives
JP2007508241A (ja) 2003-07-31 2007-04-05 バイエル・フアーマシユーチカルズ・コーポレーシヨン Ｐｄｅ１０ａ阻害剤を用いる糖尿病および関連障害の処置方法
NL2000397C2 (nl) * 2006-01-05 2007-10-30 Pfizer Prod Inc Bicyclische heteroarylverbindingen als PDE10 inhibitoren.
WO2010035745A1 (ja) * 2008-09-25 2010-04-01 杏林製薬株式会社 ヘテロ環ビアリール誘導体及びそれらを有効成分とするｐｄｅ阻害剤
WO2010059836A1 (en) * 2008-11-20 2010-05-27 Decode Genetics Ehf Substituted aza-bridged bicyclics for cardiovascular and cns disease
WO2010117926A1 (en) * 2009-04-07 2010-10-14 Schering Corporation Substituted triazolopyridines and analogs thereof
WO2011036127A1 (en) * 2009-09-24 2011-03-31 F. Hoffmann-La Roche Ag Imidazopyridine or imidazopyrimidine derivatives as phosphodiesterase 10a inhibitors
CN112019976A (zh) 2009-11-24 2020-12-01 诺基亚技术有限公司 用于处理音频信号的设备和方法
TWI485151B (zh) * 2009-12-17 2015-05-21 Lundbeck & Co As H 作為ｐｄｅ１０ａ酵素抑制劑之雜芳香族苯基咪唑衍生物
TW201200516A (en) * 2009-12-17 2012-01-01 Lundbeck & Co As H Phenylimidazole derivatives comprising an ethynylene linker as PDE10A enzyme inhibitors
TWI487705B (zh) * 2009-12-17 2015-06-11 Lundbeck & Co As H 作為ｐｄｅ１０ａ酵素抑制劑之雜芳香族芳基三唑衍生物

Also Published As

Publication number Publication date
UA108711C2 (uk) 2015-05-25
US8946427B2 (en) 2015-02-03
AU2012311713A1 (en) 2014-03-13
EP2758396A1 (en) 2014-07-30
IL231403A0 (en) 2014-04-30
CN103827114A (zh) 2014-05-28
US9227970B2 (en) 2016-01-05
KR20140075716A (ko) 2014-06-19
WO2013041472A1 (en) 2013-03-28
MX2014003025A (es) 2014-05-28
KR101584925B1 (ko) 2016-01-12
US20150099735A1 (en) 2015-04-09
EA201490599A1 (ru) 2014-07-30
CN103827114B (zh) 2016-08-24
CA2846758C (en) 2017-09-12
US20140303141A1 (en) 2014-10-09
CO6900144A2 (es) 2014-03-20
PE20141553A1 (es) 2014-10-30
JP2014526533A (ja) 2014-10-06
CA2846758A1 (en) 2013-03-28
CL2014000641A1 (es) 2014-11-14
BR112014006248A2 (pt) 2017-04-11
EP2758396B1 (en) 2017-03-29
SG11201400759RA (en) 2014-07-30
NZ621597A (en) 2015-04-24

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