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PE20050765A1 - DERIVADOS DE SULFONAMIDA COMO AGONISTAS DE LOS RECEPTORES ß2 ADRENERGICOS - Google Patents

DERIVADOS DE SULFONAMIDA COMO AGONISTAS DE LOS RECEPTORES ß2 ADRENERGICOS

Info

Publication number
PE20050765A1
PE20050765A1 PE2005000078A PE2005000078A PE20050765A1 PE 20050765 A1 PE20050765 A1 PE 20050765A1 PE 2005000078 A PE2005000078 A PE 2005000078A PE 2005000078 A PE2005000078 A PE 2005000078A PE 20050765 A1 PE20050765 A1 PE 20050765A1
Authority
PE
Peru
Prior art keywords
hydroxy
phenyl
amino
adrenergic receptors
methylsulfonyl
Prior art date
Application number
PE2005000078A
Other languages
English (en)
Inventor
Alan Daniel Brown
Kim James
Ian Brian Moses
Nicholas Murray Thomson
Charlotte Alice Louise Lane
Original Assignee
Pfizer
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=43063961&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20050765(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from GB0406388A external-priority patent/GB0406388D0/en
Application filed by Pfizer filed Critical Pfizer
Publication of PE20050765A1 publication Critical patent/PE20050765A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C323/00Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
    • C07C323/23Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
    • C07C323/39Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton at least one of the nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom
    • C07C323/40Y being a hydrogen or a carbon atom
    • C07C323/42Y being a carbon atom of a six-membered aromatic ring
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/08Bronchodilators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/16Central respiratory analeptics
    • 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
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • 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
    • C07C311/01Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
    • C07C311/02Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C311/08Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/02Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
    • C07D295/027Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring
    • C07D295/03Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring with the ring nitrogen atoms directly attached to acyclic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/12Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14The ring being saturated
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2602/00Systems containing two condensed rings
    • C07C2602/02Systems containing two condensed rings the rings having only two atoms in common
    • C07C2602/04One of the condensed rings being a six-membered aromatic ring
    • C07C2602/08One of the condensed rings being a six-membered aromatic ring the other ring being five-membered, e.g. indane

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pulmonology (AREA)
  • Immunology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)
  • Pyridine Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

SE REFIERE A DERIVADOS DE SULFONAMIDA DE FORMULA I DONDE EL GRUPO (CH2)n-C(=O)Q1 ESTA EN POSICION RELATIVA META O PARA, R1 Y R2 SE SELECCIONAN DE H Y ALQUILO C1-C4, n ES 0,1 O 2 Y Q1 ES UN GRUPO a DONDE p ES 1-2 ; R3, R4, R5 ,R6 SON IGUALES O DIFERENTES Y SE SELECCIONAN DE H, ALQUILO C1-C4- OR8 ,R8 ES ALQUILO C1-C4. SON COMPUESTOS PREFERIDOS: N-BENCIL-2-(3-{2-[((2R)-2-HIDROXI-2-{4-HIDROXI-3-[(METILSULFONIL)AMINO]FENIL}-ETIL)AMINO]-2-METILPROPIL}FENIL)ACETAMIDA; 2-(3-{2-[((2R)-2-HIDROXI-2-{4-HIDROXI-3-[(METILSULFONIL)AMINO]FENIL}ETIL)AMINO]-2-METILPROPIL}FENIL)-N-(4-METOXIBENCIL)ACETAMIDA; 2-(3-{2-[((2R)-2-HIDROXI-2-{4-HIDROXI-3-[(METILSULFONIL)AMINO]FENIL}ETIL)AMINO]-2-METILPROPIL}FENIL)-N-(2-METOXIBENCIL)ACETAMIDA. SE REFIERE TAMBIEN A UN PROCESO PARA LA PREPARACION. LOS COMPUESTOS MENCIONADOS SON ANTAGONISTAS DE LOS RECEPTORES ß2 ADRENERGICOS UTILES EN EL TRATAMIENTO DE ENFERMEDADES ALERGICAS DE LAS VIAS RESPIRATORIAS
PE2005000078A 2004-01-22 2005-01-20 DERIVADOS DE SULFONAMIDA COMO AGONISTAS DE LOS RECEPTORES ß2 ADRENERGICOS PE20050765A1 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP04290168 2004-01-22
GB0406388A GB0406388D0 (en) 2004-03-22 2004-03-22 Sulfonamide derivatives for the treatment of diseases
US60025904P 2004-08-09 2004-08-09

Publications (1)

Publication Number Publication Date
PE20050765A1 true PE20050765A1 (es) 2005-10-31

Family

ID=43063961

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2005000078A PE20050765A1 (es) 2004-01-22 2005-01-20 DERIVADOS DE SULFONAMIDA COMO AGONISTAS DE LOS RECEPTORES ß2 ADRENERGICOS

Country Status (40)

Country Link
US (1) US7351742B2 (es)
EP (1) EP1708992B1 (es)
JP (1) JP4036343B2 (es)
KR (1) KR100785580B1 (es)
CN (1) CN1910144B (es)
AP (1) AP2378A (es)
AR (1) AR047510A1 (es)
AT (1) ATE369333T1 (es)
AU (1) AU2005214154B2 (es)
BR (1) BRPI0507041A (es)
CA (1) CA2553293C (es)
CO (1) CO5720993A2 (es)
CY (1) CY1106894T1 (es)
DE (1) DE602005001929T2 (es)
DK (1) DK1708992T3 (es)
DO (1) DOP2005000004A (es)
EA (1) EA009735B1 (es)
EC (1) ECSP066701A (es)
ES (1) ES2289691T3 (es)
GE (1) GEP20084452B (es)
HN (1) HN2005000030A (es)
HR (1) HRP20070452T3 (es)
IL (1) IL176629A (es)
MA (1) MA28303A1 (es)
ME (1) ME00557A (es)
MY (1) MY139690A (es)
NL (1) NL1028086C2 (es)
NO (1) NO20063761L (es)
NZ (1) NZ548235A (es)
OA (1) OA13361A (es)
PA (1) PA8621901A1 (es)
PE (1) PE20050765A1 (es)
PL (1) PL1708992T3 (es)
PT (1) PT1708992E (es)
RS (1) RS50538B (es)
SI (1) SI1708992T1 (es)
TW (1) TWI273099B (es)
UA (1) UA82283C2 (es)
UY (1) UY28724A1 (es)
WO (1) WO2005080324A1 (es)

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EP1924553A1 (en) 2005-08-08 2008-05-28 Argenta Discovery Limited Bicyclo[2.2.]hept-7-ylamine derivatives and their uses
GB0601951D0 (en) 2006-01-31 2006-03-15 Novartis Ag Organic compounds
NZ570693A (en) 2006-03-20 2011-02-25 Pfizer Ltd Amine derivatives
KR20080110925A (ko) 2006-04-21 2008-12-19 노파르티스 아게 아데노신 a2a 수용체 효능제로서 사용하기 위한 퓨린 유도체
BRPI0719270A2 (pt) * 2006-10-04 2014-03-11 Pfizer Ltd Derivados de sulfonamida como agonistas adrenérgicos e antagonistas muscarínicos
DE102007018151A1 (de) 2007-04-16 2008-10-23 Günenthal GmbH Neue Vanilloid-Rezeptor Liganden und ihre Verwendung zur Herstellung von Arzneimitteln
US7713463B1 (en) * 2007-11-13 2010-05-11 Nuvasive, Inc. Method of manufacturing embroidered surgical implants
KR20100113557A (ko) 2008-01-11 2010-10-21 노파르티스 아게 키나제 억제제로서의 피리미딘
US8263623B2 (en) * 2008-07-11 2012-09-11 Pfizer Inc. Triazol derivatives useful for the treatment of diseases
US8236786B2 (en) 2008-08-07 2012-08-07 Pulmagen Therapeutics (Inflammation) Limited Respiratory disease treatment
PT2379507E (pt) 2008-12-30 2014-01-21 Pulmagen Therapeutics Inflammation Ltd Compostos de sulfonamida para o tratamento de desordens respiratórias
ES2635358T3 (es) 2009-04-23 2017-10-03 Theravance Respiratory Company, Llc Compuestos de diamina que tienen actividad antagonista del receptor muscarínico y agonista del receptor beta2 adrenérgico
CN102448978A (zh) 2009-05-29 2012-05-09 辉瑞有限公司 新颖的糖皮质激素受体激动剂
WO2010150014A1 (en) 2009-06-24 2010-12-29 Pulmagen Therapeutics (Inflammation) Limited 5r- 5 -deuterated glitazones for respiratory disease treatment
JP5801997B2 (ja) 2009-07-07 2015-10-28 ファイザー・リミテッドPfizer Limited 薬品の組合せを吸入するための投薬ユニット、投薬ユニットのパック、および吸入器
GB0918922D0 (en) 2009-10-28 2009-12-16 Vantia Ltd Aminopyridine derivatives
GB0918924D0 (en) 2009-10-28 2009-12-16 Vantia Ltd Azaindole derivatives
GB0918923D0 (en) 2009-10-28 2009-12-16 Vantia Ltd Aminothiazole derivatives
WO2011098746A1 (en) 2010-02-09 2011-08-18 Pulmagen Therapeutics (Inflammation) Limited Crystalline acid addition salts of ( 5r) -enanti0mer of pioglitazone
GB201002243D0 (en) 2010-02-10 2010-03-31 Argenta Therapeutics Ltd Respiratory disease treatment
GB201002224D0 (en) 2010-02-10 2010-03-31 Argenta Therapeutics Ltd Respiratory disease treatment
WO2012034095A1 (en) 2010-09-09 2012-03-15 Irm Llc Compounds and compositions as trk inhibitors
US8637516B2 (en) 2010-09-09 2014-01-28 Irm Llc Compounds and compositions as TRK inhibitors
US9102671B2 (en) 2011-02-25 2015-08-11 Novartis Ag Compounds and compositions as TRK inhibitors
PE20141614A1 (es) 2011-06-10 2014-11-20 Chiesi Farma Spa Compuestos con actividad antagonista de los receptores muscarinicos y actividad agonista del receptor beta2 adrenergico
PE20151216A1 (es) 2012-12-06 2015-09-08 Chiesi Farma Spa Compuestos con actividad antagonista de los receptores muscarinicos y actividad agonista del receptor beta2 adrenergico
BR112015012746A2 (pt) 2012-12-06 2017-07-11 Chiesi Farm Spa compostos que possuem atividade de antagonista de receptores muscarínicos e agonista de receptores beta2-adrenérgicos
AU2021296221A1 (en) 2020-06-26 2023-02-02 Mylan Pharma Uk Limited Formulations including 5-(3-(3-hydroxyphenoxy)azetidin-1-yl)-5-methyl-2,2-diphenylhexanamide

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Also Published As

Publication number Publication date
DE602005001929T2 (de) 2007-12-06
JP4036343B2 (ja) 2008-01-23
PA8621901A1 (es) 2006-03-24
UA82283C2 (uk) 2008-03-25
NO20063761L (no) 2006-10-23
AP2378A (en) 2012-03-08
HRP20070452T3 (hr) 2008-02-29
MA28303A1 (fr) 2006-11-01
ECSP066701A (es) 2006-10-31
IL176629A0 (en) 2006-10-31
EA009735B1 (ru) 2008-02-28
KR20060127073A (ko) 2006-12-11
GEP20084452B (en) 2008-08-10
WO2005080324A1 (en) 2005-09-01
CO5720993A2 (es) 2007-01-31
ES2289691T3 (es) 2008-02-01
HN2005000030A (es) 2009-04-20
CA2553293A1 (en) 2005-09-01
EP1708992A1 (en) 2006-10-11
CA2553293C (en) 2010-12-14
DOP2005000004A (es) 2005-07-31
AR047510A1 (es) 2006-01-25
AU2005214154A1 (en) 2005-09-01
UY28724A1 (es) 2005-08-31
EP1708992B1 (en) 2007-08-08
IL176629A (en) 2011-04-28
JP2007518790A (ja) 2007-07-12
WO2005080324A8 (en) 2006-02-23
RS50538B (sr) 2010-05-07
NZ548235A (en) 2010-05-28
KR100785580B1 (ko) 2007-12-13
TWI273099B (en) 2007-02-11
HK1096083A1 (en) 2007-05-25
SI1708992T1 (sl) 2007-12-31
NL1028086A1 (nl) 2005-07-25
AU2005214154B2 (en) 2008-01-24
CN1910144A (zh) 2007-02-07
US20050171147A1 (en) 2005-08-04
TW200530164A (en) 2005-09-16
MY139690A (en) 2009-10-30
EA200601141A1 (ru) 2007-02-27
ATE369333T1 (de) 2007-08-15
DE602005001929D1 (de) 2007-09-20
AP2006003671A0 (en) 2006-06-30
US7351742B2 (en) 2008-04-01
BRPI0507041A (pt) 2007-06-12
DK1708992T3 (da) 2007-11-05
CY1106894T1 (el) 2012-09-26
OA13361A (en) 2007-04-13
PL1708992T3 (pl) 2007-12-31
NL1028086C2 (nl) 2006-05-09
ME00557A (en) 2011-12-20
PT1708992E (pt) 2007-11-16
CN1910144B (zh) 2010-06-09

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