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MA37618B1 - Dérivés pontés fluorés de spiro[2.4]heptane en tant qu'agonistes de récepteur alx - Google Patents

Dérivés pontés fluorés de spiro[2.4]heptane en tant qu'agonistes de récepteur alx

Info

Publication number
MA37618B1
MA37618B1 MA37618A MA37618A MA37618B1 MA 37618 B1 MA37618 B1 MA 37618B1 MA 37618 A MA37618 A MA 37618A MA 37618 A MA37618 A MA 37618A MA 37618 B1 MA37618 B1 MA 37618B1
Authority
MA
Morocco
Prior art keywords
heptane
fluor
receptor agonists
alx receptor
bridged derivatives
Prior art date
Application number
MA37618A
Other languages
English (en)
Other versions
MA37618A1 (fr
Inventor
Olivier Corminboeuf
Davide Pozzi
Original Assignee
Actelion Pharmaceuticals Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Actelion Pharmaceuticals Ltd filed Critical Actelion Pharmaceuticals Ltd
Publication of MA37618A1 publication Critical patent/MA37618A1/fr
Publication of MA37618B1 publication Critical patent/MA37618B1/fr

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory 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
    • 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
    • A61P25/04—Centrally acting analgesics, e.g. opioids
    • 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
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A61P29/02—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] without antiinflammatory effect
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A61P31/18—Antivirals for RNA viruses for HIV
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/08—Antiallergic agents
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/14—Nitrogen atoms not forming part of a nitro radical
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/56—Nitrogen atoms
    • C07D211/58—Nitrogen atoms attached in position 4

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Immunology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Virology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Pulmonology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Hospice & Palliative Care (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Psychiatry (AREA)
  • AIDS & HIV (AREA)
  • Molecular Biology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Hydrogenated Pyridines (AREA)
  • Pyrrole Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

La présente invention concerne des dérivés pontés fluorés de spiro[2.4]heptane de formule (i), où n et r
MA37618A 2012-05-16 2013-05-14 Dérivés pontés fluorés de spiro[2.4]heptane en tant qu'agonistes de récepteur alx MA37618B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP12168322 2012-05-16
PCT/IB2013/053976 WO2013171694A1 (fr) 2012-05-16 2013-05-15 Dérivés pontés fluorés de spiro[2.4]heptane en tant qu'agonistes de récepteur alx

Publications (2)

Publication Number Publication Date
MA37618A1 MA37618A1 (fr) 2016-12-30
MA37618B1 true MA37618B1 (fr) 2017-08-31

Family

ID=48699893

Family Applications (1)

Application Number Title Priority Date Filing Date
MA37618A MA37618B1 (fr) 2012-05-16 2013-05-14 Dérivés pontés fluorés de spiro[2.4]heptane en tant qu'agonistes de récepteur alx

Country Status (23)

Country Link
US (1) US9139524B2 (fr)
EP (1) EP2850060B1 (fr)
JP (1) JP6101789B2 (fr)
KR (1) KR20150013285A (fr)
CN (1) CN104321309B (fr)
AR (1) AR091059A1 (fr)
AU (1) AU2013261091B2 (fr)
BR (1) BR112014028358A2 (fr)
CA (1) CA2871336A1 (fr)
CL (1) CL2014002918A1 (fr)
EA (1) EA025264B1 (fr)
ES (1) ES2595219T3 (fr)
HK (1) HK1208441A1 (fr)
IL (1) IL235660A0 (fr)
MA (1) MA37618B1 (fr)
MX (1) MX355221B (fr)
NZ (1) NZ702971A (fr)
PH (1) PH12014502465A1 (fr)
PL (1) PL2850060T3 (fr)
SG (1) SG11201406971WA (fr)
TW (1) TWI579269B (fr)
WO (1) WO2013171694A1 (fr)
ZA (1) ZA201409249B (fr)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012066488A2 (fr) 2010-11-17 2012-05-24 Actelion Pharmaceuticals Ltd Dérivés à ponts ester de spiro [2.4] heptane
MX2013006420A (es) 2010-12-07 2013-07-29 Actelion Pharmaceuticals Ltd Derivados de aminotriazol hidrolixado como agonistas del receptor de alx.
EP2850058B1 (fr) 2012-05-16 2016-07-13 Actelion Pharmaceuticals Ltd. Dérivés de 1- (p-tolyl) cyclopropyl substituted bridged spiro [2,4] heptane en tant qu' agonistes du récepteur alx.
AR096686A1 (es) 2013-06-25 2016-01-27 Actelion Pharmaceuticals Ltd Derivados de espiro[2.4]heptano puenteados sustituidos con difluoroetil-oxazol como agonistas del receptor de alx
AU2014292064B2 (en) 2013-07-18 2018-07-05 Idorsia Pharmaceuticals Ltd Piperazine substituted bridged spiro[2.4]heptane derivatives as alx receptor agonists
AR097279A1 (es) 2013-08-09 2016-03-02 Actelion Pharmaceuticals Ltd Derivados de benzimidazolil-metil urea como agonistas del receptor de alx
NZ725044A (en) 2014-05-13 2019-03-29 Novartis Ag Compounds and compositions for inducing chondrogenesis
CA2987235A1 (fr) 2015-05-27 2016-12-01 Kyorin Pharmaceutical Co., Ltd. Derive de l'uree ou sel pharmacologiquement acceptable de ce dernier
WO2016189877A1 (fr) 2015-05-27 2016-12-01 Kyorin Pharmaceutical Co., Ltd. Dérivé d'urée ou sel pharmacologiquement acceptable de ce dernier
CN111233751B (zh) * 2020-03-25 2021-02-02 丽水绿氟科技有限公司 一种3,3-二氟-4-氨基哌啶类化合物及其衍生物的制备方法

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09500133A (ja) * 1993-07-16 1997-01-07 メルク エンド カンパニー インコーポレーテッド オキシトシンのアンタゴニストである置換ピペラジニル樟脳誘導体
WO2003082314A2 (fr) 2002-04-03 2003-10-09 Bayer Healthcare Ag Diagnostics et therapies pour maladies liees a un recepteur de type 1 de peptides n-formyl (fprl1)
US20080234305A1 (en) 2003-10-09 2008-09-25 Olivier Bezencon Novel Tetrahydropyridine Derivatives
JP2007516434A (ja) 2003-11-07 2007-06-21 アカディア ファーマシューティカルズ インコーポレイティド リポキシン受容体ｆｐｒｌ１の、疼痛および炎症の治療に有効な化合物を識別する手段としての使用
TW200538098A (en) 2004-03-22 2005-12-01 Astrazeneca Ab Therapeutic agents
US7820699B2 (en) 2005-04-27 2010-10-26 Hoffmann-La Roche Inc. Cyclic amines
US20100144751A1 (en) 2007-03-28 2010-06-10 Array Biopharma Inc. IMIDAZO[1,2-a]PYRIDINE COMPOUNDS AS RECEPTOR TYROSINE KINASE INHIBITORS
AR069650A1 (es) 2007-12-14 2010-02-10 Actelion Pharmaceuticals Ltd Derivados de aminopirazol como agonistas no peptidicos del receptor alx humano
CA2706839C (fr) 2007-12-18 2015-10-20 Actelion Pharmaceuticals Ltd Derives d'aminotriazole comme agonistes d'alx
SI2432760T1 (sl) * 2009-05-18 2013-10-30 Actelion Pharmaceuticals Ltd. Premoĺ äśeni derivati spiro (2.4) heptana kot alx-receptorji in/ali fprl2-agonisti
BRPI1010738A8 (pt) 2009-06-09 2017-12-26 Actelion Pharmaceuticals Ltd Derivados de aminotriazol fluorado
JP5624130B2 (ja) 2009-06-12 2014-11-12 アクテリオンファーマシューティカルズ リミテッドＡｃｔｅｌｉｏｎ Ｐｈａｒｍａｃｅｕｔｉｃａｌｓ Ｌｔｄ Ａｌｘ受容体アゴニストとしてのオキサゾール及びチアゾール誘導体
CA2803920A1 (fr) * 2010-06-24 2011-12-29 Richard Beard Derives d'acides cycloalkyl- et cycloalcenyl-1,2-dicarboxyliques presentant une activite agoniste ou antagoniste du recepteur fprl-1
WO2012066488A2 (fr) 2010-11-17 2012-05-24 Actelion Pharmaceuticals Ltd Dérivés à ponts ester de spiro [2.4] heptane
MX2013006420A (es) 2010-12-07 2013-07-29 Actelion Pharmaceuticals Ltd Derivados de aminotriazol hidrolixado como agonistas del receptor de alx.
ES2526132T3 (es) 2010-12-07 2015-01-07 Actelion Pharmaceuticals Ltd. Derivados de oxazolil-metiléter como agonistas del receptor de ALX
AU2012282977A1 (en) * 2011-07-11 2014-02-06 Allergan, Inc. Polycyclic pyrrolidine-2,5-dione derivatives as -formyl peptide receptor like-1 (FPRLl-1) receptor modulators
EP2850058B1 (fr) 2012-05-16 2016-07-13 Actelion Pharmaceuticals Ltd. Dérivés de 1- (p-tolyl) cyclopropyl substituted bridged spiro [2,4] heptane en tant qu' agonistes du récepteur alx.
RU2696487C2 (ru) 2013-03-06 2019-08-02 Аллерган, Инк. Применение агонистов формилпептидного рецептора 2 для лечения дерматологических заболеваний
CN105007909B (zh) 2013-03-06 2019-06-28 阿勒根公司 用于治疗眼部炎性疾病的甲酰基肽受体2激动剂的用途

Also Published As

Publication number Publication date
CN104321309B (zh) 2016-06-22
ES2595219T3 (es) 2016-12-28
EP2850060A1 (fr) 2015-03-25
HK1208441A1 (en) 2016-03-04
EA025264B1 (ru) 2016-12-30
MA37618A1 (fr) 2016-12-30
PL2850060T3 (pl) 2017-01-31
NZ702971A (en) 2016-09-30
IL235660A0 (en) 2015-02-01
BR112014028358A2 (pt) 2020-07-21
CN104321309A (zh) 2015-01-28
WO2013171694A1 (fr) 2013-11-21
EA201401259A1 (ru) 2015-04-30
US20150118258A1 (en) 2015-04-30
TW201348198A (zh) 2013-12-01
PH12014502465A1 (en) 2014-12-22
AU2013261091A1 (en) 2015-01-22
TWI579269B (zh) 2017-04-21
MX2014013829A (es) 2015-02-04
AU2013261091B2 (en) 2017-04-06
CL2014002918A1 (es) 2015-02-06
ZA201409249B (en) 2016-09-28
SG11201406971WA (en) 2014-11-27
EP2850060B1 (fr) 2016-07-13
JP2015516463A (ja) 2015-06-11
AR091059A1 (es) 2014-12-30
KR20150013285A (ko) 2015-02-04
US9139524B2 (en) 2015-09-22
CA2871336A1 (fr) 2013-11-21
MX355221B (es) 2018-04-10
JP6101789B2 (ja) 2017-03-22

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