BR9913939A - Composto, processo para a preparação do mesmo, uso do mesmo, composição farmacêutica, e, método para o tratamento da dor, febre ou inflamação - Google Patents

Composto, processo para a preparação do mesmo, uso do mesmo, composição farmacêutica, e, método para o tratamento da dor, febre ou inflamação

Info

Publication number
BR9913939A
BR9913939A BR9913939-1A BR9913939A BR9913939A BR 9913939 A BR9913939 A BR 9913939A BR 9913939 A BR9913939 A BR 9913939A BR 9913939 A BR9913939 A BR 9913939A
Authority
BR
Brazil
Prior art keywords
group
alkyl
compound
pharmaceutical composition
hydroxycarbonyl
Prior art date
Application number
BR9913939-1A
Other languages
English (en)
Inventor
Maria Isabel Crespo Crespo
Juan Miguel Jimenez Mayorga
Carles Puig Duran
Lidia Soca Pueyo
Original Assignee
Almirall Prodesfarma 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 claimed from ES9802011A external-priority patent/ES2154561B1/es
Priority claimed from ES009900619A external-priority patent/ES2168895A1/es
Application filed by Almirall Prodesfarma Sa filed Critical Almirall Prodesfarma Sa
Publication of BR9913939A publication Critical patent/BR9913939A/pt

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00Drugs for disorders of the muscular or neuromuscular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/22Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms
    • C07C311/29Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C317/00Sulfones; Sulfoxides
    • C07C317/24Sulfones; Sulfoxides having sulfone or sulfoxide groups and doubly-bound oxygen atoms bound to the same carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/34Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D309/36Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with oxygen atoms directly attached to ring carbon atoms
    • C07D309/38Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with oxygen atoms directly attached to ring carbon atoms one oxygen atom in position 2 or 4, e.g. pyrones
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/34Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D309/36Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with oxygen atoms directly attached to ring carbon atoms
    • C07D309/40Oxygen atoms attached in positions 3 and 4, e.g. maltol
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/04Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Neurology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Rheumatology (AREA)
  • Hospice & Palliative Care (AREA)
  • Pain & Pain Management (AREA)
  • Psychiatry (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyrane Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

"COMPOSTO, PROCESSO PARA A PREPARAçãO DO MESMO, USO DO MESMO, E, COMPOSIçãO FARMACêUTICA" Derivados de 2-fenilpiran-4-ona da fórmula (I) onde R¹ representa um grupo alquila ou NR^ 4^R^ 5^, onde R^ 4^ e R^ 5^ cada um deles independentemente representa um átomo de hidrogênio ou um grupo alquila; R² representa um grupo alquila, cicloalquila C~ 3~-C~ 7~, piridila, tienila, naftila, tetrahidronaftila ou indanila, ou um grupo fenila o qual pode ser insubstituido ou substituído por um ou mais átomos de halogênio ou grupos alquila, trifluormetila, hidroxi, alcoxi, metiltio, amino, mono -ou dialquilamino, hidroxialquila ou hidroxicarbonila; R³ representa um grupo metila, hidroximetila, alcoximetila, cicloalcoximetila C~ 3~-C~ 7~, benziloximetila, hidroxicarbonila, nitrila, trifluormetila ou difluormetila ou um grupo CH~ 2~-R^ 6^ onde R representa um grupo alquila; e X representa uma ligação só, um átomo de oxigênio, um átomo de enxofre ou um grupo metileno; ou sais farmaceuticamente aceitáveis dos mesmos, processos para a sua produção e intermediários sintéticos utilizados nos referidos processos, composições farmacêuticas contendo os mesmos e seu uso em tratamentos médicos.
BR9913939-1A 1998-09-25 1999-09-16 Composto, processo para a preparação do mesmo, uso do mesmo, composição farmacêutica, e, método para o tratamento da dor, febre ou inflamação BR9913939A (pt)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
ES9802011A ES2154561B1 (es) 1998-09-25 1998-09-25 Derivados de 2-fenilpiran-4-ona.
ES009900619A ES2168895A1 (es) 1999-03-26 1999-03-26 Derivados de 2-fenilpiran-4-ona.
PCT/EP1999/006873 WO2000018753A1 (en) 1998-09-25 1999-09-16 2-phenylpyran-4-one derivatives

Publications (1)

Publication Number Publication Date
BR9913939A true BR9913939A (pt) 2001-06-12

Family

ID=26155180

Family Applications (1)

Application Number Title Priority Date Filing Date
BR9913939-1A BR9913939A (pt) 1998-09-25 1999-09-16 Composto, processo para a preparação do mesmo, uso do mesmo, composição farmacêutica, e, método para o tratamento da dor, febre ou inflamação

Country Status (34)

Country Link
US (1) US6518303B2 (pt)
EP (1) EP1115716B1 (pt)
JP (1) JP4717211B2 (pt)
KR (1) KR100806684B1 (pt)
CN (1) CN1202104C (pt)
AR (1) AR021826A1 (pt)
AT (1) ATE230405T1 (pt)
AU (1) AU765653B2 (pt)
BG (1) BG65308B1 (pt)
BR (1) BR9913939A (pt)
CA (1) CA2345069C (pt)
CO (1) CO5140127A1 (pt)
CZ (1) CZ300357B6 (pt)
DE (1) DE69904738T2 (pt)
DK (1) DK1115716T3 (pt)
EE (1) EE04812B1 (pt)
EG (1) EG23802A (pt)
ES (1) ES2190252T3 (pt)
HK (1) HK1034961A1 (pt)
HU (1) HUP0104620A3 (pt)
ID (1) ID28624A (pt)
IL (1) IL142087A0 (pt)
MX (1) MXPA01003069A (pt)
MY (1) MY121793A (pt)
NO (1) NO327987B1 (pt)
NZ (1) NZ510625A (pt)
PE (1) PE20001067A1 (pt)
PL (1) PL346895A1 (pt)
RU (1) RU2232158C2 (pt)
SI (1) SI1115716T1 (pt)
SK (1) SK286471B6 (pt)
TR (1) TR200100852T2 (pt)
TW (1) TW587079B (pt)
WO (1) WO2000018753A1 (pt)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PE20011333A1 (es) 2000-03-16 2002-01-16 Almirall Prodesfarma Ag Derivados de 2-fenilpiran-4-ona como inhibidores de ciclooxigenasa 2
US20040147581A1 (en) * 2002-11-18 2004-07-29 Pharmacia Corporation Method of using a Cox-2 inhibitor and a 5-HT1A receptor modulator as a combination therapy
ES2214129B1 (es) * 2003-02-13 2005-12-01 Almirall Prodesfarma, S.A. 3-fenilfuran-2-onas.
ES2214130B1 (es) * 2003-02-13 2005-12-01 Almirall Prodesfarma, S.A. 2-3'-bipiridinas.
ES2213485B1 (es) * 2003-02-13 2005-12-16 Almirall Prodesfarma, S.A. Derivados de la 2-fenilpiran-4-ona.
US20040220155A1 (en) * 2003-03-28 2004-11-04 Pharmacia Corporation Method of providing a steroid-sparing benefit with a cyclooxygenase-2 inhibitor and compositions therewith
US20050014729A1 (en) * 2003-07-16 2005-01-20 Pharmacia Corporation Method for the treatment or prevention of dermatological disorders with a cyclooxygenase-2 inhibitor alone and in combination with a dermatological treatment agent and compositions therewith
US20050119262A1 (en) * 2003-08-21 2005-06-02 Pharmacia Corporation Method for preventing or treating an optic neuropathy with a cox-2 inhibitor and an intraocular pressure reducing agent
US20050107350A1 (en) * 2003-08-22 2005-05-19 Pharmacia Corporation Method for the treatment or prevention of bone disorders with a cyclooxygenase-2 inhibitor alone and in combination with a bone disorder treatment agent and compositions therewith
US20050187278A1 (en) * 2003-08-28 2005-08-25 Pharmacia Corporation Treatment or prevention of vascular disorders with Cox-2 inhibitors in combination with cyclic AMP-specific phosphodiesterase inhibitors
WO2005023189A2 (en) * 2003-09-03 2005-03-17 Pharmacia Corporation Method of cox-2 selective inhibitor and nitric oxide-donating agent
US20240165148A1 (en) 2021-03-15 2024-05-23 Saul Yedgar Hyaluronic acid-conjugated dipalmitoyl phosphatidyl ethanolamine in combination with non-steroidal anti-inflammatory drugs (nsaids) for treating or alleviating inflammatory diseases

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US304728A (en) * 1884-09-09 Maubice hellwig
CH524614A (de) * 1969-12-31 1972-06-30 Ciba Geigy Ag Verfahren zur Herstellung von neuen Imidazolderivaten
US3901908A (en) * 1970-12-28 1975-08-26 Ciba Geigy Corp 2-alkyl- and 2-cycloalkyl-4,5-bis-phenyl-imidazoles
US4304728A (en) * 1979-04-05 1981-12-08 Lilly Industries Limited 6-Substituted pyranone compounds and their use as pharmaceuticals
IL59748A (en) 1979-04-05 1983-11-30 Lilly Industries Ltd 5-substituted pyranone derivatives,their production and pharmaceutical compositions containing them
JPS5834446B2 (ja) * 1979-05-22 1983-07-27 三省製薬株式会社 消炎剤
JPH0768234B2 (ja) * 1989-12-14 1995-07-26 久光製薬株式会社 コウジ酸エステル誘導体
EP0489877B1 (en) * 1990-06-29 1995-09-20 The Upjohn Company Antiatherosclerotic and antithrombotic 2-amino-6-phenyl-4h-pyran-4-ones
JPH04173391A (ja) * 1990-11-07 1992-06-22 Sanyo Chem Ind Ltd 感熱記録用増感剤および感熱記録用材料
DE4103904C2 (de) * 1991-02-08 1995-06-14 Analyticon Ges Fuer Chemische Neue Arzneimittel aus Gamma-Pyronen, Gamma-Pyridonen sowie Gamma-Thiopyronen
US6048850A (en) 1992-09-22 2000-04-11 Young; Donald A. Method of inhibiting prostaglandin synthesis in a human host
WO1995014014A2 (en) * 1993-11-19 1995-05-26 Parke, Davis & Company Pyrone derivatives as protease inhibitors and antiviral agents
US5521213A (en) * 1994-08-29 1996-05-28 Merck Frosst Canada, Inc. Diaryl bicyclic heterocycles as inhibitors of cyclooxygenase-2
US5541204A (en) 1994-12-02 1996-07-30 Bristol-Myers Squibb Company Aryloxypropanolamine β 3 adrenergic agonists
EA199700209A1 (ru) 1995-04-04 1998-04-30 Глаксо Груп Лимитед ПРОИЗВОДНЫЕ ИМИДАЗО[1,2-a]ПИРИДИНА
CA2224517A1 (en) * 1995-06-12 1996-12-27 G.D. Searle & Co. Compositions comprising a cyclooxygenase-2 inhibitor and a 5-lipoxygenase inhibitor
BR9813998A (pt) * 1997-11-19 2000-09-26 Kowa Co Novos derivados de piridazina e produtos medicinais contendo os mesmos como ingredientes efetivos

Also Published As

Publication number Publication date
CN1202104C (zh) 2005-05-18
EP1115716B1 (en) 2003-01-02
AR021826A1 (es) 2002-08-07
EE200100173A (et) 2002-08-15
EG23802A (en) 2007-08-22
ES2190252T3 (es) 2003-07-16
NZ510625A (en) 2002-12-20
MY121793A (en) 2006-02-28
TR200100852T2 (tr) 2001-10-22
WO2000018753A1 (en) 2000-04-06
US6518303B2 (en) 2003-02-11
NO20011512L (no) 2001-05-25
PL346895A1 (en) 2002-03-11
BG105373A (en) 2001-11-30
ATE230405T1 (de) 2003-01-15
CZ20011058A3 (cs) 2001-08-15
ID28624A (id) 2001-06-21
US20020045644A1 (en) 2002-04-18
CA2345069A1 (en) 2000-04-06
CO5140127A1 (es) 2002-03-22
PE20001067A1 (es) 2000-10-23
CA2345069C (en) 2009-03-10
AU6084799A (en) 2000-04-17
EP1115716A1 (en) 2001-07-18
DE69904738T2 (de) 2003-04-30
IL142087A0 (en) 2002-03-10
HUP0104620A3 (en) 2003-01-28
SK286471B6 (sk) 2008-11-06
MXPA01003069A (es) 2002-07-02
HK1034961A1 (en) 2001-11-09
CN1324352A (zh) 2001-11-28
KR100806684B1 (ko) 2008-02-26
SI1115716T1 (en) 2003-06-30
SK3702001A3 (en) 2001-12-03
KR20010075369A (ko) 2001-08-09
DE69904738D1 (de) 2003-02-06
BG65308B1 (bg) 2008-01-31
NO20011512D0 (no) 2001-03-23
HUP0104620A2 (hu) 2002-04-29
CZ300357B6 (cs) 2009-04-29
EE04812B1 (et) 2007-04-16
NO327987B1 (no) 2009-11-02
JP4717211B2 (ja) 2011-07-06
RU2232158C2 (ru) 2004-07-10
DK1115716T3 (da) 2003-02-24
JP2002525364A (ja) 2002-08-13
AU765653B2 (en) 2003-09-25
TW587079B (en) 2004-05-11

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Legal Events

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B25A Requested transfer of rights approved

Free format text: ALMIRALL PRODESFARMA AG (CH)

B08F Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette]

Free format text: REFERENTE A 6A ANUIDADE.

B08H Application fees: decision cancelled [chapter 8.8 patent gazette]

Free format text: REFERENTE AO DESPACHO PUBLICADO NA RPI 1849 DE 13/06/2006 POR TER SIDO APRESENTADA PAPELETA DE ESCLARECIMENTO.

B07A Application suspended after technical examination (opinion) [chapter 7.1 patent gazette]
B15K Others concerning applications: alteration of classification

Free format text: ALTERADA DE INT.CL: C07D 309/38, C07D 309/40, C07D 405/04, C07D 409/04, A61K 31/35, A61P 29/00, C07C 317/24, C07C 311/29

Ipc: C07D 309/38 (2008.04), C07D 309/40 (2008.04), C07D

B25D Requested change of name of applicant approved

Owner name: ALMIRALL AG (CH)

Free format text: ALTERADO DE: ALMIRALL PRODESFARMA AG

B25A Requested transfer of rights approved

Owner name: LABORATORIOS ALMIRALL, S.A. (ES)

Free format text: TRANSFERIDO DE: ALMIRALL AG

B09B Patent application refused [chapter 9.2 patent gazette]

Free format text: INDEFERIMENTO DO PRESENTE PEDIDO, UMA VEZ QUE NAO ATENDE AOS ARTIGOS 8O E 13 DA LPI

B15K Others concerning applications: alteration of classification

Free format text: ALTERADA DE INT.CL: C07D 309/38, C07D 309/40, C07D 405/04, C07D 409/04, A61K 31/35, C07C 317/24, C07C 311/29

Ipc: C07D 309/38 (2009.01), C07D 309/40 (2009.01), C07D

B12B Appeal against refusal [chapter 12.2 patent gazette]