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AR047509A1 - Derivados de sulfonamida como antagonistas de receptores adrenergicos beta2 - Google Patents

Derivados de sulfonamida como antagonistas de receptores adrenergicos beta2

Info

Publication number
AR047509A1
AR047509A1 ARP050100205A ARP050100205A AR047509A1 AR 047509 A1 AR047509 A1 AR 047509A1 AR P050100205 A ARP050100205 A AR P050100205A AR P050100205 A ARP050100205 A AR P050100205A AR 047509 A1 AR047509 A1 AR 047509A1
Authority
AR
Argentina
Prior art keywords
group
alkyl
optionally substituted
sulfonamide derivatives
antagonists
Prior art date
Application number
ARP050100205A
Other languages
English (en)
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=36954179&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR047509(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from GB0406387A external-priority patent/GB0406387D0/en
Application filed by Pfizer filed Critical Pfizer
Publication of AR047509A1 publication Critical patent/AR047509A1/es

Links

Classifications

    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/18Sulfonamides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/35Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/352Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline 
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52Purines, e.g. adenine
    • A61K31/522Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
    • 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
    • A61P37/00Drugs for immunological or allergic disorders
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D217/00Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/02Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
    • C07D217/06Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines with the ring nitrogen atom acylated by carboxylic or carbonic acids, or with sulfur or nitrogen analogues thereof, e.g. carbamates
    • 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

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pulmonology (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

La presente se refiere a derivados de sulfonamida como antagonistas de receptores adrenérgicos beta 2, procedimientos para su preparacion, composiciones farmacéuticas que los contienen y usos para trastornos y afecciones inflamatorias, alérgicas y respiratorias. Reivindicacion 1: Un compuesto de formula general (1) en la que el grupo (CH2)n-C(=O)Q1 está en posicion meta o para, R1 y R2 se seleccionan independientemente entre H y alquilo C1-4, n es 0, 1 o 2 y Q1 es un grupo seleccionado entre las formulas (2) o (3) y un grupo *-NR8-Q2-A, donde p es 1 o 2; Q2 es un alquileno C1-4 opcionalmente sustituido con un grupo hidroxi, R8 es H o alquilo C1-4 y A es piridilo opcionalmente sustituido con OH, cicloalquilo C3-7 opcionalmente sustituido con OH o un grupo de formula (4) o (5) en el que R3, R4, R5, R6 y R7 son iguales o diferentes y se seleccionan entre H, alquilo C1-4, OR9, SR9, halo, CN, CF3, OCF3, COOR9, SO2NR9R10, CONR9R10, NR9R10, NHCOR10 y fenilo opcionalmente sustituido con 1 a 3 grupos seleccionados entre OR9, halo y alquilo C1-4, donde R9 y R10 son iguales o diferentes y se seleccionan entre H o alquilo C1-4 y el * representa el punto de union al grupo carbonilo; donde el grupo Q1 está sustituido al menos con un grupo hidroxi; o, si es apropiado, sus sales farmacéuticamente aceptables y/o isomeros, tautomeros, solvatos o variaciones isotopicas de los mismos.
ARP050100205A 2004-01-22 2005-01-20 Derivados de sulfonamida como antagonistas de receptores adrenergicos beta2 AR047509A1 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP04290169 2004-01-22
GB0406387A GB0406387D0 (en) 2004-03-22 2004-03-22 Sulfonamide derivatives for the treatment of diseases
US60026004P 2004-08-09 2004-08-09

Publications (1)

Publication Number Publication Date
AR047509A1 true AR047509A1 (es) 2006-01-25

Family

ID=36954179

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP050100205A AR047509A1 (es) 2004-01-22 2005-01-20 Derivados de sulfonamida como antagonistas de receptores adrenergicos beta2

Country Status (30)

Country Link
US (4) US7244766B2 (es)
EP (1) EP1708991B1 (es)
JP (1) JP4020954B2 (es)
AP (1) AP2359A (es)
AR (1) AR047509A1 (es)
AT (1) ATE375977T1 (es)
AU (1) AU2005214153B2 (es)
BR (1) BRPI0507085A (es)
CA (1) CA2553789C (es)
DE (1) DE602005002930T2 (es)
DK (1) DK1708991T3 (es)
DO (1) DOP2005000006A (es)
EA (1) EA011167B1 (es)
ES (1) ES2293530T3 (es)
GE (1) GEP20094781B (es)
MY (1) MY143390A (es)
NL (1) NL1028087C2 (es)
NO (1) NO20062983L (es)
NZ (1) NZ548318A (es)
OA (1) OA13362A (es)
PA (1) PA8622001A1 (es)
PE (1) PE20051136A1 (es)
PL (1) PL1708991T3 (es)
PT (1) PT1708991E (es)
RS (1) RS50561B (es)
SI (1) SI1708991T1 (es)
TW (1) TWI341831B (es)
UA (1) UA84048C2 (es)
UY (1) UY28721A1 (es)
WO (1) WO2005080313A2 (es)

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NZ548318A (en) * 2004-01-22 2009-03-31 Pfizer Sulfonamide derivatives for the treatment of diseases
GB0425054D0 (en) * 2004-03-23 2004-12-15 Pfizer Ltd Formamide derivatives for the treatment of diseases
GT200500281A (es) 2004-10-22 2006-04-24 Novartis Ag Compuestos organicos.
EP1695973A1 (en) * 2005-02-24 2006-08-30 Neuro3D Ocaperidone salt and pharmaceutical compositions containing the same
WO2007010356A2 (en) * 2005-07-18 2007-01-25 Pfizer Limited Process for the preparation of sulfonamide derivatives
GB0516313D0 (en) 2005-08-08 2005-09-14 Argenta Discovery Ltd Azole derivatives and their uses
EP2281813A1 (en) 2005-08-08 2011-02-09 Pulmagen Therapeutics (Synergy) Limited Bicyclo[2.2.1]hept-7-ylamine derivatives and their uses
GB0601951D0 (en) 2006-01-31 2006-03-15 Novartis Ag Organic compounds
HRP20120494T1 (hr) 2006-04-21 2012-08-31 Novartis Ag Derivati purina za uporabu kao agonista adenozin a2a receptora
JP4948913B2 (ja) * 2006-06-16 2012-06-06 上野製薬株式会社 ナフタレンカルボン酸アミドの製造方法
WO2009087224A1 (en) 2008-01-11 2009-07-16 Novartis Ag Pyrimidines as kinase inhibitors
US8236786B2 (en) 2008-08-07 2012-08-07 Pulmagen Therapeutics (Inflammation) Limited Respiratory disease treatment
PL2379507T3 (pl) 2008-12-30 2014-03-31 Pulmagen Therapeutics Inflammation Ltd Związki sulfonamidu do leczenia zaburzeń układu oddechowego
AU2010252609A1 (en) 2009-05-29 2011-11-10 Pfizer Limited Novel glucocorticoid receptor agonists
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
GB0918924D0 (en) 2009-10-28 2009-12-16 Vantia Ltd Azaindole derivatives
GB0918923D0 (en) 2009-10-28 2009-12-16 Vantia Ltd Aminothiazole derivatives
GB0918922D0 (en) 2009-10-28 2009-12-16 Vantia Ltd Aminopyridine 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
UY33597A (es) 2010-09-09 2012-04-30 Irm Llc Compuestos y composiciones como inhibidores de la trk
JP5959541B2 (ja) 2011-02-25 2016-08-02 ノバルティス アーゲー Trk阻害剤としてのピラゾロ[1,5−a]ピリジン
WO2013021309A1 (en) 2011-08-11 2013-02-14 Pfizer Limited Intermediate and process for the preparation of a sulfonamide derivative
CN116033893A (zh) 2020-06-26 2023-04-28 迈兰制药英国有限公司 包含5-[3-(3-羟基苯氧基)氮杂环丁烷-1-基]-5-甲基-2,2-二苯基己酰胺的制剂

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Also Published As

Publication number Publication date
NL1028087C2 (nl) 2006-05-09
UA84048C2 (ru) 2008-09-10
BRPI0507085A (pt) 2007-06-19
WO2005080313A3 (en) 2005-12-01
MY143390A (en) 2011-05-13
PE20051136A1 (es) 2006-02-18
US20100273758A1 (en) 2010-10-28
PT1708991E (pt) 2007-12-14
AP2006003669A0 (en) 2006-06-30
NL1028087A1 (nl) 2005-07-25
JP4020954B2 (ja) 2007-12-12
DE602005002930T2 (de) 2008-07-24
SI1708991T1 (sl) 2008-02-29
US20050182091A1 (en) 2005-08-18
WO2005080313A9 (en) 2006-08-31
CA2553789C (en) 2011-07-19
US20080267970A1 (en) 2008-10-30
CA2553789A1 (en) 2005-09-01
JP2007518789A (ja) 2007-07-12
AU2005214153B2 (en) 2008-09-18
US7767715B2 (en) 2010-08-03
US8013019B2 (en) 2011-09-06
EA011167B1 (ru) 2009-02-27
DOP2005000006A (es) 2005-07-31
US20090197912A1 (en) 2009-08-06
PL1708991T3 (pl) 2008-02-29
DK1708991T3 (da) 2008-01-14
RS50561B (sr) 2010-05-07
AU2005214153A1 (en) 2005-09-01
TWI341831B (en) 2011-05-11
OA13362A (en) 2007-04-13
TW200530165A (en) 2005-09-16
DE602005002930D1 (de) 2007-11-29
UY28721A1 (es) 2005-08-31
ATE375977T1 (de) 2007-11-15
NO20062983L (no) 2006-07-24
GEP20094781B (en) 2009-09-25
EP1708991B1 (en) 2007-10-17
WO2005080313A2 (en) 2005-09-01
AP2359A (en) 2012-01-30
EP1708991A2 (en) 2006-10-11
ES2293530T3 (es) 2008-03-16
NZ548318A (en) 2009-03-31
US7244766B2 (en) 2007-07-17
US7528170B2 (en) 2009-05-05
EA200601223A1 (ru) 2006-12-29
PA8622001A1 (es) 2005-08-30

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