ES2251866B1 - Nuevos derivados de piridazin-3(2h)-ona. - Google Patents

Nuevos derivados de piridazin-3(2h)-ona. Download PDF

Info

Publication number
ES2251866B1
ES2251866B1 ES200401500A ES200401500A ES2251866B1 ES 2251866 B1 ES2251866 B1 ES 2251866B1 ES 200401500 A ES200401500 A ES 200401500A ES 200401500 A ES200401500 A ES 200401500A ES 2251866 B1 ES2251866 B1 ES 2251866B1
Authority
ES
Spain
Prior art keywords
ethyl
oxo
carboxylate
ylamino
dihydropyridazin
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Fee Related
Application number
ES200401500A
Other languages
English (en)
Spanish (es)
Other versions
ES2251866A1 (es
Inventor
Maria Antonia Buil Albero
Vittorio Dal Piaz
Yolanda Garrido
Jordi Gracia Ferrer
Luis Miguel Pages Santacana
Joan Taltavull Moll
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Almirall SA
Original Assignee
Laboratorios Almirall SA
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
Priority to ES200401500A priority Critical patent/ES2251866B1/es
Application filed by Laboratorios Almirall SA filed Critical Laboratorios Almirall SA
Priority to PCT/EP2005/006304 priority patent/WO2005123692A1/en
Priority to UY28958A priority patent/UY28958A1/es
Priority to UAA200700279A priority patent/UA88472C2/ru
Priority to RU2007101654/04A priority patent/RU2376293C2/ru
Priority to JP2007515846A priority patent/JP2008502628A/ja
Priority to US11/629,522 priority patent/US7960383B2/en
Priority to DE602005025478T priority patent/DE602005025478D1/de
Priority to CNA2005800187731A priority patent/CN1964952A/zh
Priority to BRPI0511383-0A priority patent/BRPI0511383A/pt
Priority to KR1020077001216A priority patent/KR20070029808A/ko
Priority to AT05751683T priority patent/ATE492538T1/de
Priority to AU2005254659A priority patent/AU2005254659A1/en
Priority to EP05751683A priority patent/EP1758869B1/en
Priority to SG200906039-3A priority patent/SG155909A1/en
Priority to MXPA06013593A priority patent/MXPA06013593A/es
Priority to CA002570170A priority patent/CA2570170A1/en
Priority to ES05751683T priority patent/ES2358335T3/es
Priority to PE2005000683A priority patent/PE20060436A1/es
Priority to ARP050102489A priority patent/AR049402A1/es
Priority to TW094120336A priority patent/TW200612951A/zh
Publication of ES2251866A1 publication Critical patent/ES2251866A1/es
Priority to ZA200609403A priority patent/ZA200609403B/xx
Priority to IL179734A priority patent/IL179734A0/en
Priority to EC2006007058A priority patent/ECSP067058A/es
Priority to NO20070321A priority patent/NO20070321L/no
Application granted granted Critical
Publication of ES2251866B1 publication Critical patent/ES2251866B1/es
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50—Pyridazines; Hydrogenated pyridazines
    • A61K31/501—Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50—Pyridazines; Hydrogenated pyridazines
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • 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
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/02—Nasal agents, e.g. decongestants
    • 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
    • A61P11/06—Antiasthmatics
    • 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
    • A61P11/16—Central respiratory analeptics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/06—Antipsoriatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00—Drugs for disorders of the muscular or neuromuscular system
    • A61P21/04—Drugs for disorders of the muscular or neuromuscular system for myasthenia gravis
    • 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
    • A61P25/24—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
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • 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
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • 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
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • 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
    • A61P39/00—General protective or antinoxious agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P39/00—General protective or antinoxious agents
    • A61P39/06—Free radical scavengers or antioxidants
    • 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
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/12—Antidiuretics, e.g. drugs for diabetes insipidus
    • 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
    • C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three 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
    • C07D237/24—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pulmonology (AREA)
  • Immunology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Rheumatology (AREA)
  • Dermatology (AREA)
  • Epidemiology (AREA)
  • Toxicology (AREA)
  • Diabetes (AREA)
  • Pain & Pain Management (AREA)
  • Psychiatry (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Hospice & Palliative Care (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Ophthalmology & Optometry (AREA)
  • Biochemistry (AREA)
  • Transplantation (AREA)
  • Otolaryngology (AREA)
  • Urology & Nephrology (AREA)
  • Hematology (AREA)
ES200401500A 2004-06-18 2004-06-18 Nuevos derivados de piridazin-3(2h)-ona. Expired - Fee Related ES2251866B1 (es)

Priority Applications (25)

Application Number Priority Date Filing Date Title
ES200401500A ES2251866B1 (es) 2004-06-18 2004-06-18 Nuevos derivados de piridazin-3(2h)-ona.
MXPA06013593A MXPA06013593A (es) 2004-06-18 2005-06-13 Nuevos derivados de piridazin-3(2h)-ona.
UAA200700279A UA88472C2 (en) 2004-06-18 2005-06-13 Pyridazin-3(2h)-one derivatives and their use as pde4 inhibitors
RU2007101654/04A RU2376293C2 (ru) 2004-06-18 2005-06-13 Производные пиридазин-3(2h)-она и их применение в качестве ингибиторов фдэ4
JP2007515846A JP2008502628A (ja) 2004-06-18 2005-06-13 ピリダジン−3(2h)−オン誘導体およびpde4の阻害剤としてのそれらの使用
US11/629,522 US7960383B2 (en) 2004-06-18 2005-06-13 Pyridazin-3(2H)-one derivatives and their use as PDE4 inhibitors
DE602005025478T DE602005025478D1 (de) 2004-06-18 2005-06-13 Pyridazin-3(2h)-on derivate und ihre verwendung als pde4 inhibitoren
CNA2005800187731A CN1964952A (zh) 2004-06-18 2005-06-13 哒嗪-3(2h)-酮衍生物及其作为pde4抑制剂的用途
BRPI0511383-0A BRPI0511383A (pt) 2004-06-18 2005-06-13 composto, composição farmacêutica, uso de composto, método para o tratamento de um sujeito que sofre com uma condição patológica ou doença susceptìvel de melhora por inibição de fosfodiesterase 4 e produto combinado
UY28958A UY28958A1 (es) 2004-06-18 2005-06-13 Nuevos derivados de piridazin-3(2h)-ona
AT05751683T ATE492538T1 (de) 2004-06-18 2005-06-13 Pyridazin-3(2h)-on derivate und ihre verwendung als pde4 inhibitoren
AU2005254659A AU2005254659A1 (en) 2004-06-18 2005-06-13 Pyridazin-3(2H)-one derivatives and their use as PDE4 inhibitors
PCT/EP2005/006304 WO2005123692A1 (en) 2004-06-18 2005-06-13 Pyridazin-3(2h)-one derivatives and their use as pde4 inhibitors
SG200906039-3A SG155909A1 (en) 2004-06-18 2005-06-13 Pyridazin-3(2h)-one derivatives and their use as pde4 inhibitors
ES05751683T ES2358335T3 (es) 2004-06-18 2005-06-13 Derivados de piridazin-3(2h)-ona y su uso como inhibidores de pde4.
EP05751683A EP1758869B1 (en) 2004-06-18 2005-06-13 Pyridazin-3(2h)-one derivatives and their use as pde4 inhibitors
CA002570170A CA2570170A1 (en) 2004-06-18 2005-06-13 Pyridazin-3(2h)-one derivatives and their use as pde4 inhibitors
KR1020077001216A KR20070029808A (ko) 2004-06-18 2005-06-13 피리다진-3(2h)-온 유도체 및 pde4 저해제로서의이들의 용도
PE2005000683A PE20060436A1 (es) 2004-06-18 2005-06-15 Derivados de piridazin-3(2h)-ona como inhibidores de pde4
ARP050102489A AR049402A1 (es) 2004-06-18 2005-06-17 Derivados de piridazin-3-(2h)-ona
TW094120336A TW200612951A (en) 2004-06-18 2005-06-17 New pyridazin-3(2h)-one derivatives
ZA200609403A ZA200609403B (en) 2004-06-18 2006-11-13 Pyridazin-3(2H)-one derivatives and their use as PDE4 inhibitors
IL179734A IL179734A0 (en) 2004-06-18 2006-11-30 Pyridazin-3(2h)-one derivatives and their use as pde4 inhibitors
EC2006007058A ECSP067058A (es) 2004-06-18 2006-12-08 Nuevos derivados de piridazin-3(2h)-ona
NO20070321A NO20070321L (no) 2004-06-18 2007-01-17 Pyridazin-3(2H)-on-derivater og deres anvendelse som PDE4-inhibitorer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
ES200401500A ES2251866B1 (es) 2004-06-18 2004-06-18 Nuevos derivados de piridazin-3(2h)-ona.

Publications (2)

Publication Number Publication Date
ES2251866A1 ES2251866A1 (es) 2006-05-01
ES2251866B1 true ES2251866B1 (es) 2007-06-16

Family

ID=34956035

Family Applications (2)

Application Number Title Priority Date Filing Date
ES200401500A Expired - Fee Related ES2251866B1 (es) 2004-06-18 2004-06-18 Nuevos derivados de piridazin-3(2h)-ona.
ES05751683T Expired - Lifetime ES2358335T3 (es) 2004-06-18 2005-06-13 Derivados de piridazin-3(2h)-ona y su uso como inhibidores de pde4.

Family Applications After (1)

Application Number Title Priority Date Filing Date
ES05751683T Expired - Lifetime ES2358335T3 (es) 2004-06-18 2005-06-13 Derivados de piridazin-3(2h)-ona y su uso como inhibidores de pde4.

Country Status (24)

Country Link
US (1) US7960383B2 (cg-RX-API-DMAC10.html)
EP (1) EP1758869B1 (cg-RX-API-DMAC10.html)
JP (1) JP2008502628A (cg-RX-API-DMAC10.html)
KR (1) KR20070029808A (cg-RX-API-DMAC10.html)
CN (1) CN1964952A (cg-RX-API-DMAC10.html)
AR (1) AR049402A1 (cg-RX-API-DMAC10.html)
AT (1) ATE492538T1 (cg-RX-API-DMAC10.html)
AU (1) AU2005254659A1 (cg-RX-API-DMAC10.html)
BR (1) BRPI0511383A (cg-RX-API-DMAC10.html)
CA (1) CA2570170A1 (cg-RX-API-DMAC10.html)
DE (1) DE602005025478D1 (cg-RX-API-DMAC10.html)
EC (1) ECSP067058A (cg-RX-API-DMAC10.html)
ES (2) ES2251866B1 (cg-RX-API-DMAC10.html)
IL (1) IL179734A0 (cg-RX-API-DMAC10.html)
MX (1) MXPA06013593A (cg-RX-API-DMAC10.html)
NO (1) NO20070321L (cg-RX-API-DMAC10.html)
PE (1) PE20060436A1 (cg-RX-API-DMAC10.html)
RU (1) RU2376293C2 (cg-RX-API-DMAC10.html)
SG (1) SG155909A1 (cg-RX-API-DMAC10.html)
TW (1) TW200612951A (cg-RX-API-DMAC10.html)
UA (1) UA88472C2 (cg-RX-API-DMAC10.html)
UY (1) UY28958A1 (cg-RX-API-DMAC10.html)
WO (1) WO2005123692A1 (cg-RX-API-DMAC10.html)
ZA (1) ZA200609403B (cg-RX-API-DMAC10.html)

Families Citing this family (54)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2211344B1 (es) * 2002-12-26 2005-10-01 Almirall Prodesfarma, S.A. Nuevos derivados de piridazin-3(2h)-ona.
KR101190912B1 (ko) 2003-11-19 2012-10-12 어레이 바이오파마 인크. Mek의 헤테로시클릭 억제제 및 그의 사용 방법
US7732616B2 (en) * 2003-11-19 2010-06-08 Array Biopharma Inc. Dihydropyridine and dihydropyridazine derivatives as inhibitors of MEK and methods of use thereof
US7517994B2 (en) * 2003-11-19 2009-04-14 Array Biopharma Inc. Heterocyclic inhibitors of MEK and methods of use thereof
ES2251866B1 (es) 2004-06-18 2007-06-16 Laboratorios Almirall S.A. Nuevos derivados de piridazin-3(2h)-ona.
ES2251867B1 (es) * 2004-06-21 2007-06-16 Laboratorios Almirall S.A. Nuevos derivados de piridazin-3(2h)-ona.
TWI441637B (zh) 2005-05-18 2014-06-21 Array Biopharma Inc Mek雜環抑制劑及其使用方法
ES2265276B1 (es) 2005-05-20 2008-02-01 Laboratorios Almirall S.A. Derivados de 4-(2-amino-1-hidroxietil)fenol como agonistas del receptor beta2 adrenergico.
JO2769B1 (en) 2005-10-26 2014-03-15 جانسين فارماسوتيكا ان. في Rapid decomposition of physiologically antagonistic agents of the 2-dopamine receptor
JO2849B1 (en) 2007-02-13 2015-03-15 جانسين فارماسوتيكا ان. في Dopamine 2 receptor antagonists are rapidly hydrolyzed
ES2320955B1 (es) 2007-03-02 2010-03-16 Laboratorios Almirall S.A. Nuevos derivados de 3-((1,2,4)triazolo(4,3-a)piridin-7-il)benzamida.
ES2320954B1 (es) * 2007-03-02 2010-03-16 Laboratorio Almirall S.A. Nuevo procedimiento de preparacion de 3-metil-4-fenilisoxazolo (3,4-d)iridazin-7(6h)-ona.
RU2489431C2 (ru) 2007-04-23 2013-08-10 Янссен Фармацевтика Н.В. Тиа(диа)золы как быстро диссоциирующие антагонисты рецептора допамина 2
JP5431305B2 (ja) 2007-04-23 2014-03-05 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ 高速解離性ドパミン2受容体アンタゴニストとしての4−アルコキシピリダジン誘導体
EP2096105A1 (en) 2008-02-28 2009-09-02 Laboratorios Almirall, S.A. Derivatives of 4-(2-amino-1-hydroxyethyl)phenol as agonists of the b2 adrenergic receptor
EP2100598A1 (en) 2008-03-13 2009-09-16 Laboratorios Almirall, S.A. Inhalation composition containing aclidinium for treatment of asthma and chronic obstructive pulmonary disease
EP2100599A1 (en) 2008-03-13 2009-09-16 Laboratorios Almirall, S.A. Inhalation composition containing aclidinium for treatment of asthma and chronic obstructive pulmonary disease
EP2108641A1 (en) 2008-04-11 2009-10-14 Laboratorios Almirall, S.A. New substituted spiro[cycloalkyl-1,3'-indo]-2'(1'H)-one derivatives and their use as p38 mitogen-activated kinase inhibitors
EP2113503A1 (en) 2008-04-28 2009-11-04 Laboratorios Almirall, S.A. New substituted indolin-2-one derivatives and their use as p39 mitogen-activated kinase inhibitors
EA019048B1 (ru) 2008-07-31 2013-12-30 Янссен Фармацевтика Нв Пиперазин-1-илтрифторметилзамещенные пиридины в качестве быстро диссоциирующихся антагонистов d-рецепторов дофамина
UY32297A (es) 2008-12-22 2010-05-31 Almirall Sa Sal mesilato de 5-(2-{[6-(2,2-difluoro-2-fenilitoxi) hexil]amino}-1-hidroxietil)-8-hidroxiquinolin-2( 1h)-ona como agonista del receptor b(beta)2 acrenérgico
EP2221297A1 (en) 2009-02-18 2010-08-25 Almirall, S.A. 5-(2-{[6-(2,2-difluoro-2-phenylethoxy)hexyl]amino}-1-hydroxyethyl)-8-hydroxyquinolin-2(1h)-one and its use in the treatment of pulmonary diseases
EP2221055A1 (en) 2009-02-18 2010-08-25 Almirall, S.A. 5-(2-{[6-(2,2-difluoro-2-phenylethoxy)hexyl]amino}-1-hydroxyethyl)-8-hydroxyquinolin-2(1H)-one for the treatment of lung function
EP2228368A1 (en) 2009-03-12 2010-09-15 Almirall, S.A. Process for manufacturing 5-(2-{[6-(2,2-difluoro-2-phenylethoxy) hexyl]amino}-1-hydroxyethyl)-8-hydroxyquinolin-2(1H)-one
EP2338888A1 (en) 2009-12-24 2011-06-29 Almirall, S.A. Imidazopyridine derivatives as JAK inhibitors
EP2360158A1 (en) 2010-02-18 2011-08-24 Almirall, S.A. Pyrazole derivatives as jak inhibitors
UY33213A (es) 2010-02-18 2011-09-30 Almirall Sa Derivados de pirazol como inhibidores de jak
EP2386555A1 (en) 2010-05-13 2011-11-16 Almirall, S.A. New cyclohexylamine derivatives having beta2 adrenergic agonist and m3 muscarinic antagonist activities
EP2397482A1 (en) 2010-06-15 2011-12-21 Almirall, S.A. Heteroaryl imidazolone derivatives as jak inhibitors
EP2441755A1 (en) 2010-09-30 2012-04-18 Almirall, S.A. Pyridine- and isoquinoline-derivatives as Syk and JAK kinase inhibitors
EP2457900A1 (en) 2010-11-25 2012-05-30 Almirall, S.A. New pyrazole derivatives having CRTh2 antagonistic behaviour
EP2463289A1 (en) 2010-11-26 2012-06-13 Almirall, S.A. Imidazo[1,2-b]pyridazine derivatives as JAK inhibitors
EP2489663A1 (en) 2011-02-16 2012-08-22 Almirall, S.A. Compounds as syk kinase inhibitors
EP2518070A1 (en) 2011-04-29 2012-10-31 Almirall, S.A. Pyrrolotriazinone derivatives as PI3K inhibitors
EP2518071A1 (en) 2011-04-29 2012-10-31 Almirall, S.A. Imidazopyridine derivatives as PI3K inhibitors
EP2527344A1 (en) 2011-05-25 2012-11-28 Almirall, S.A. Pyridin-2(1H)-one derivatives useful as medicaments for the treatment of myeloproliferative disorders, transplant rejection, immune-mediated and inflammatory diseases
EP2526945A1 (en) 2011-05-25 2012-11-28 Almirall, S.A. New CRTH2 Antagonists
EP2548876A1 (en) 2011-07-18 2013-01-23 Almirall, S.A. New CRTh2 antagonists
EP2548863A1 (en) 2011-07-18 2013-01-23 Almirall, S.A. New CRTh2 antagonists.
EP2554544A1 (en) 2011-08-01 2013-02-06 Almirall, S.A. Pyridin-2(1h)-one derivatives as jak inhibitors
EP2578570A1 (en) 2011-10-07 2013-04-10 Almirall, S.A. Novel process for preparing 5-(2-{[6-(2,2-difluoro-2-phenylethoxy)hexyl]amino}-1(r)-hydroxyethyl)-8-hydroxyquinolin-2(1h)-one via novel intermediates of synthesis.
EP2592077A1 (en) 2011-11-11 2013-05-15 Almirall, S.A. New cyclohexylamine derivatives having beta2 adrenergic agonist and M3 muscarinic antagonist activities
EP2592078A1 (en) 2011-11-11 2013-05-15 Almirall, S.A. New cyclohexylamine derivatives having beta2 adrenergic agonist and M3 muscarinic antagonist activities
EP2641900A1 (en) 2012-03-20 2013-09-25 Almirall, S.A. Novel polymorphic Crystal forms of 5-(2-{[6-(2,2-difluoro-2-phenylethoxy) hexyl]amino}-1-(R)-hydroxyethyl)-8-hydroxyquinolin-2(1h)-one, heminapadisylate as agonist of the ß2 adrenergic receptor.
EP2647627A1 (en) 2012-04-02 2013-10-09 Almirall, S.A. Salts of 5-[(1r)-2-({2-[4-(2,2-difluoro-2-phenylethoxy)phenyl] ethyl}amino)-1-hydroxyethyl]-8-hydroxyquinolin-2(1h)-one.
EP2666465A1 (en) 2012-05-25 2013-11-27 Almirall, S.A. Novel dosage and formulation
EP2668941A1 (en) 2012-05-31 2013-12-04 Almirall, S.A. Novel dosage form and formulation of abediterol
WO2014060431A1 (en) 2012-10-16 2014-04-24 Almirall, S.A. Pyrrolotriazinone derivatives as pi3k inhibitors
KR101282885B1 (ko) * 2012-11-14 2013-07-05 한국원자력연구원 스티릴피리다진온 유도체를 이용한 아밀로이드 단백질 응집물의 검출 방법
EP2738172A1 (en) 2012-11-28 2014-06-04 Almirall, S.A. New bicyclic compounds as crac channel modulators
LT2931275T (lt) 2012-12-17 2022-06-27 Almirall S.A. Aklidiniumas, skirtas naudoti fizinio aktyvumo kasdieniniame gyvenime padidinimui pacientui, sergančiam lėtine obstrukcine plaučių liga
ES2750523T3 (es) 2012-12-18 2020-03-26 Almirall Sa Derivados de ciclohexil y quinuclidinil carbamato que tienen actividades de agonista beta2 adrenérgicos y antagonistas muscarínicos M3
TW201446767A (zh) 2013-02-15 2014-12-16 Almirall Sa 作為磷脂肌醇3-激酶抑製劑之吡咯並三嗪衍生物
EP2848615A1 (en) 2013-07-03 2015-03-18 Almirall, S.A. New pyrazole derivatives as CRAC channel modulators

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003097613A1 (en) * 2002-05-16 2003-11-27 Almirall Prodesfarma Sa Pyridazin-3(2h)-one derivatives as pde4 inhibitors

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU405344A1 (ru) 1970-06-01 1975-08-25 Всесоюзный научно-исследовательский химико-фармацевтический институт им. С.Орджоникидзе Способ получени производных 3-замещенных 5-(2-оксифениламино)-пиридазона-6
GB1351569A (en) 1972-05-15 1974-05-01 Morishita Pharma 2-alkyl-4-alkoxy-5-morpholino-3-2h-pyridazinones and their method of preparation
DE2225218C2 (de) 1972-05-24 1983-01-13 Morishita Pharmaceutical Co., Ltd., Osaka 2-Alkyl-4-äthoxy-5-morpholino-3(2H)-pyridazinone und Verfahren zu deren Herstellung
JP3245165B2 (ja) 1991-10-09 2002-01-07 シンテックス(ユー・エス・エイ)・インコーポレイテッド ピリドピリダジノンおよびピリダジンチオン化合物
US5679696A (en) 1992-07-28 1997-10-21 Rhone-Poulenc Rorer Limited Compounds containing phenyl linked to aryl or heteroaryl by an aliphatic-or heteroatom-containing linking group
RU2182574C2 (ru) * 1995-06-20 2002-05-20 Зенека Лимитед Ароматические соединения и содержащие их фармацевтические композиции
TW502026B (en) * 1995-06-20 2002-09-11 Zeneca Ltd Aromatic compounds useful as antagonists of e-type prostaglandins, processes for the preparation thereof, pharmaceutical compositions comprising the compounds, and intermediates
DE19533975A1 (de) 1995-09-14 1997-03-20 Merck Patent Gmbh Arylalkyl-diazinone
DE19540475A1 (de) 1995-10-20 1997-04-24 Schering Ag Chirale Methylphenyloxazolidinone
HUP0100042A3 (en) 1996-05-20 2003-01-28 Darwin Discovery Ltd Cambridge Benzofuran carboxamides medicaments containing the same and their therapeutic use
NZ332341A (en) 1996-05-20 2000-05-26 Darwin Discovery Ltd Quinoline carboxamides as TNF inhibitors and as PDE-IV inhibitors
ES2137113B1 (es) 1997-07-29 2000-09-16 Almirall Prodesfarma Sa Nuevos derivados de triazolo-piridazinas heterociclicos.
KR20010024268A (ko) 1997-11-25 2001-03-26 로즈 암스트롱 Pde-iv의 벤젠술폰아미드 억제제 및 그들의 치료학적용도
PL198503B1 (pl) 1998-10-27 2008-06-30 Abbott Lab Związki pirydazynonowe, kompozycje farmaceutyczne je zawierające oraz ich zastosowanie
WO2000050402A1 (en) 1999-02-25 2000-08-31 Merck Frosst Canada & Co. Pde iv inhibiting compounds, compositions and methods of treatment
JP2000247959A (ja) * 1999-02-26 2000-09-12 Kowa Co ピリダジン−3−オン誘導体及びこれを含有する医薬
US6313156B1 (en) 1999-12-23 2001-11-06 Icos Corporation Thiazole compounds as cyclic-AMP-specific phosphodiesterase inhibitors
CN1471515A (zh) 2000-06-05 2004-01-28 ��̹��ҽҩ��˾ 作为β2-肾上腺素受体激动剂及PDE-4抑制剂的有效的化合物
AU2001275401A1 (en) 2000-06-08 2001-12-17 Incyte Genomics, Inc. Intracellular signaling proteins
US6699890B2 (en) 2000-12-22 2004-03-02 Memory Pharmaceuticals Corp. Phosphodiesterase 4 inhibitors
WO2003032981A1 (en) 2001-10-16 2003-04-24 Memory Pharmaceuticals Corporation 4-(4-alkoxy-3-hydroxyphenyl)-2-pyrrolidone derivatives as pde-4 inhibitors for the treatment of neurological syndromes
AR037517A1 (es) 2001-11-05 2004-11-17 Novartis Ag Derivados de naftiridinas, un proceso para su preparacion, composicion farmaceutica y el uso de los mismos para la preparacion de un medicamento para el tratamiento de una enfermedad inflamatoria
RU2356893C2 (ru) 2002-11-19 2009-05-27 Мемори Фармасьютиклз Корпорейшн Ингибиторы фосфодиэстеразы 4
ES2211344B1 (es) 2002-12-26 2005-10-01 Almirall Prodesfarma, S.A. Nuevos derivados de piridazin-3(2h)-ona.
US7226930B2 (en) 2003-04-18 2007-06-05 Memory Pharmaceutical Corporation Phosphodiesterase 4 inhibitors
ES2232306B1 (es) 2003-11-10 2006-08-01 Almirall Prodesfarma, S.A. Nuevos derivados de piridazin-3(2h)-ona.
ES2251866B1 (es) 2004-06-18 2007-06-16 Laboratorios Almirall S.A. Nuevos derivados de piridazin-3(2h)-ona.
ES2251867B1 (es) 2004-06-21 2007-06-16 Laboratorios Almirall S.A. Nuevos derivados de piridazin-3(2h)-ona.
JP2009523805A (ja) 2006-01-17 2009-06-25 シグナル ファーマシューティカルズ,エルエルシー TNFα、PDE4及びB−RAFの阻害剤、それらの組成物及びそれらの使用法
ES2320954B1 (es) 2007-03-02 2010-03-16 Laboratorio Almirall S.A. Nuevo procedimiento de preparacion de 3-metil-4-fenilisoxazolo (3,4-d)iridazin-7(6h)-ona.

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003097613A1 (en) * 2002-05-16 2003-11-27 Almirall Prodesfarma Sa Pyridazin-3(2h)-one derivatives as pde4 inhibitors
ES2195785A1 (es) * 2002-05-16 2003-12-01 Almirall Prodesfarma Sa Nuevos derivados de piridazin-3(2h)-ona.

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
COSTANTINO, L. et al.: "Isoxazolo-(3,4-d)-pyridazin-7-(6H)-one as a potential substrate for new aldose reductase inhibitors". J. Med. Chem. 1999, vol. 42, páginas 1894-1900, tabla 3. *
DAL PIAZ, V. et al.: "4,5-functionalized 6-phenyl-3(2H)- pyridazinones: synthesis and evaluation of antinociceptive activity". Eur. J. Med. Chem. 1996, vol. 31, páginas 65-70, tabla I. *
DAL PIAZ, V. et al.: "5-Acyl-6-aryl-4-nitro-3(2H) pyridazinones and related 4-amino compounds: synthesis and pharmacological evaluation". Journal of pharmaceutical sciences, 1991, vol. 80 (4) páginas 341-348, tabla III. *

Also Published As

Publication number Publication date
ES2358335T3 (es) 2011-05-09
AR049402A1 (es) 2006-07-26
ECSP067058A (es) 2007-03-29
EP1758869A1 (en) 2007-03-07
US7960383B2 (en) 2011-06-14
WO2005123692A8 (en) 2006-05-04
ES2251866A1 (es) 2006-05-01
WO2005123692A1 (en) 2005-12-29
MXPA06013593A (es) 2007-03-15
DE602005025478D1 (de) 2011-02-03
US20080280918A1 (en) 2008-11-13
UA88472C2 (en) 2009-10-26
SG155909A1 (en) 2009-10-29
ATE492538T1 (de) 2011-01-15
CN1964952A (zh) 2007-05-16
RU2007101654A (ru) 2008-07-27
PE20060436A1 (es) 2006-06-02
BRPI0511383A (pt) 2007-12-26
NO20070321L (no) 2007-03-12
KR20070029808A (ko) 2007-03-14
EP1758869B1 (en) 2010-12-22
JP2008502628A (ja) 2008-01-31
RU2376293C2 (ru) 2009-12-20
IL179734A0 (en) 2007-05-15
ZA200609403B (en) 2007-12-27
AU2005254659A1 (en) 2005-12-29
CA2570170A1 (en) 2005-12-29
UY28958A1 (es) 2005-08-31
TW200612951A (en) 2006-05-01

Similar Documents

Publication Publication Date Title
ES2251866A1 (es) Nuevos derivados de piridazin-3(2h)-ona.
ES2251867B1 (es) Nuevos derivados de piridazin-3(2h)-ona.
ES2211344B1 (es) Nuevos derivados de piridazin-3(2h)-ona.
ES2232306B1 (es) Nuevos derivados de piridazin-3(2h)-ona.
KR20040106536A (ko) Pde4 저해제로서의 피리다진-3(2h)-온 유도체
ES2281251B1 (es) Nuevos derivados de pirido (3',2':4,5) furo (3,2-d) pirimidina.
MXPA06005101A (en) Pyridazin-3 (2h) -one derivatives and their use as pde4 inhibitors

Legal Events

Date Code Title Description
EC2A Search report published

Date of ref document: 20060501

Kind code of ref document: A1

PC2A Transfer of patent
FG2A Definitive protection

Ref document number: 2251866B1

Country of ref document: ES

FD2A Announcement of lapse in spain

Effective date: 20180809