AR074314A1 - Pirrolidinas, antagonistas de ep2 - Google Patents

Pirrolidinas, antagonistas de ep2

Info

Publication number
AR074314A1
AR074314A1 ARP090104350A ARP090104350A AR074314A1 AR 074314 A1 AR074314 A1 AR 074314A1 AR P090104350 A ARP090104350 A AR P090104350A AR P090104350 A ARP090104350 A AR P090104350A AR 074314 A1 AR074314 A1 AR 074314A1
Authority
AR
Argentina
Prior art keywords
optionally substituted
independently
aromatic rings
alkyl
alkyl optionally
Prior art date
Application number
ARP090104350A
Other languages
English (en)
Inventor
Kevin Neil Dack
James E Mills
Sarah Elizabeth Skerratt
Original Assignee
Pfizer 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 Pfizer Ltd filed Critical Pfizer Ltd
Publication of AR074314A1 publication Critical patent/AR074314A1/es

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/12Heterocyclic 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
    • 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
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • 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
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00Drugs for disorders of the endocrine system
    • A61P5/24Drugs for disorders of the endocrine system of the sex hormones
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic 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
    • C07D207/04Heterocyclic 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
    • C07D207/10Heterocyclic 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
    • C07D207/16Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Endocrinology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Diabetes (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Urology & Nephrology (AREA)
  • Reproductive Health (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyrrole Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

Se refiere a una clase de compuestos de pirrolidina e fórmula (1), y sus derivados farmacéuticamente aceptables, a su uso en medicina, a composiciones que los contienen, y a procesos para su preparación. También se refiere a intermedios utilizados en la preparación de dichos compuestos y derivados. En particular, los compuestos de fórmula (1) son útiles para el tratamiento de trastornos mediados por EP2, como la endometriosis, los fibroides uterinos (leiomiomata), la menorragia, la adenomiosis, la dismenorrea primaria y secundaria (incluyendo los síntomas de dispareunia, disquexia y dolor pélvico crónico), el síndrome del dolor pélvico crónico, la enfermedad del rinón poliquístico. Reivindicación 1: Un compuesto caracterizado porque es de fórmula (1) en la que R1 es un grupo fenilo opcionalmente sustituido con uno o dos sustituyentes seleccionados cada uno independientemente de F, CI, Br, CN, alquilo C1-4, alquiltio C1-4, alcoxi C1-4, fluoroalquilo C1-4 y fluoroalcoxi C1-4, o es un grupo cicloalquilo C3-6; X representa un enlace directo, NH u O; Z se selecciona de ¬C(=O)O-R2, ¬C(=O)NH-SO2R3 y ¬CN, R2 es H o alquilo C1-6 opcionalmente sustituido con 1 a 3 átomos de flúor; R3 es alquilo C1-6 opcionalmente sustituido con 1 a 3 átomos de flúor; Ar es un grupo aromático que consiste en 1, 2 o 3 anillos aromáticos, en los que dichos anillos aromáticos se seleccionan cada uno independientemente de fenilo y un anillo heteroaromático de 5 o 6 miembros que contiene 1, 2, 3 o 4 heteroátomos seleccionados cada uno independientemente de N, O y S, y en los que dichos anillos aromáticos, si son 2 o más, pueden estar condensados y/o enlazados por uno o más enlaces covalentes, y en los que dichos anillos aromáticos están opcionalmente sustituidos con 1, 2 o 3 sustituyentes seleccionados cada uno independientemente de F, Cl, CN, OH, alquilo C1-6, alquiltio C1-6, fluoroalquilo C1-6, fluoroalquiltio C1-6, fluoroalcoxi C1-6, alcoxi C1-6, SO2R4, NR5R6, NHSO2R7, SO2NR8R9, CONR10R11 y NHCOR12; R4 y R7 son cada uno independientemente alquilo C1-6 opcionalmente sustituido con 1 a 3 átomos de F; R5, R6, R8, R9, R10, R11 y R12 son cada uno independientemente H o alquilo C1-6 opcionalmente sustituido con 1 a 3 átomos de flúor; o su sal farmacéuticamente aceptable, solvato (incluyendo hidrato) o profármaco.
ARP090104350A 2008-11-10 2009-11-10 Pirrolidinas, antagonistas de ep2 AR074314A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US11286908P 2008-11-10 2008-11-10

Publications (1)

Publication Number Publication Date
AR074314A1 true AR074314A1 (es) 2011-01-05

Family

ID=41503565

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP090104350A AR074314A1 (es) 2008-11-10 2009-11-10 Pirrolidinas, antagonistas de ep2

Country Status (31)

Country Link
US (1) US8278343B2 (es)
EP (1) EP2364296A1 (es)
JP (1) JP2012508225A (es)
KR (1) KR20110083733A (es)
CN (1) CN102209710A (es)
AP (1) AP2011005728A0 (es)
AR (1) AR074314A1 (es)
AU (1) AU2009312427B2 (es)
BR (1) BRPI0920924A2 (es)
CA (1) CA2741589A1 (es)
CL (1) CL2011001034A1 (es)
CO (1) CO6382112A2 (es)
CR (1) CR20110217A (es)
CU (1) CU20110093A7 (es)
DO (1) DOP2011000127A (es)
EA (1) EA201100549A1 (es)
EC (1) ECSP11011032A (es)
GE (1) GEP20125607B (es)
IL (1) IL212490A0 (es)
MA (1) MA32782B1 (es)
MX (1) MX2011004903A (es)
NI (1) NI201100092A (es)
NZ (1) NZ592311A (es)
PA (1) PA8848001A1 (es)
PE (1) PE20110663A1 (es)
SV (1) SV2011003896A (es)
TN (1) TN2011000211A1 (es)
TW (1) TW201022234A (es)
UY (1) UY32228A (es)
WO (1) WO2010052625A1 (es)
ZA (1) ZA201104310B (es)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW201034675A (en) * 2008-12-18 2010-10-01 Sanofi Aventis Method for treating macular degeneration
TW201326154A (zh) 2011-11-28 2013-07-01 拜耳知識產權公司 作為ep2受體拮抗劑之新穎2h-吲唑
WO2013176220A1 (ja) * 2012-05-25 2013-11-28 国立大学法人京都大学 概日リズム調整
CN110041269A (zh) * 2019-05-16 2019-07-23 海门瑞一医药科技有限公司 一种2-氯-5-羟基嘧啶的制备方法
WO2022272062A1 (en) * 2021-06-24 2022-12-29 Reservoir Neuroscience, Inc. Ep2 antagonist compounds

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5319099A (en) * 1991-01-21 1994-06-07 Shionogi Seiyaku Kabushiki Kaisha 3-benzylidene-1-carbamoyl-2-pyrrolidone compounds useful as antiinflammatory agents
JP4554931B2 (ja) * 2001-12-20 2010-09-29 メルク セローノ ソシエテ アノニム プロスタグランジン調節物質としてのピロリジン誘導体
WO2007005176A1 (en) * 2005-06-29 2007-01-11 Allergan, Inc. Pyrrolidinones for the treatment of glaucoma and ocular hypertension
US7592364B2 (en) * 2006-02-28 2009-09-22 Allergan, Inc. Substituted gamma lactams as therapeutic agents
US7550448B2 (en) * 2006-05-24 2009-06-23 Allergan, Inc. Therapeutic compounds
DE102006039912A1 (de) * 2006-08-25 2008-03-20 Bayer Healthcare Ag Substituierte Spirotetronsäuren und ihre Verwendung
WO2008139287A1 (en) * 2007-05-10 2008-11-20 Pfizer Limited Azetidine derivatives and their use as prostaglandin e2 antagonists

Also Published As

Publication number Publication date
US8278343B2 (en) 2012-10-02
CL2011001034A1 (es) 2011-11-11
CO6382112A2 (es) 2012-02-15
JP2012508225A (ja) 2012-04-05
GEP20125607B (en) 2012-08-10
CR20110217A (es) 2011-05-12
WO2010052625A1 (en) 2010-05-14
AU2009312427B2 (en) 2011-10-20
AP2011005728A0 (en) 2011-06-30
EA201100549A1 (ru) 2011-12-30
US20100120793A1 (en) 2010-05-13
SV2011003896A (es) 2011-07-05
AU2009312427A1 (en) 2010-05-14
EP2364296A1 (en) 2011-09-14
ECSP11011032A (es) 2011-06-30
TN2011000211A1 (fr) 2012-12-17
CA2741589A1 (en) 2010-05-14
IL212490A0 (en) 2011-06-30
TW201022234A (en) 2010-06-16
NI201100092A (es) 2011-10-31
UY32228A (es) 2010-06-30
MX2011004903A (es) 2011-05-30
PE20110663A1 (es) 2011-09-23
PA8848001A1 (es) 2010-06-28
MA32782B1 (fr) 2011-11-01
DOP2011000127A (es) 2011-07-15
BRPI0920924A2 (pt) 2016-10-04
CN102209710A (zh) 2011-10-05
NZ592311A (en) 2012-12-21
ZA201104310B (en) 2012-02-29
CU20110093A7 (es) 2012-01-31
KR20110083733A (ko) 2011-07-20

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