CL2010001528A1 - Compuestos derivados del acido 7-fenoxicroman-4-carboxilico sustituido; proceso de preparacion; compuesto intermediario; composicion farmaceutica de dicho compuesto; y su uso como antagonista de los receptores de prostaglandina d2 (pgd2) para tratar trastornos inmunologicos, enfermedades alergicas, trastornos inflamatorios. - Google Patents

Compuestos derivados del acido 7-fenoxicroman-4-carboxilico sustituido; proceso de preparacion; compuesto intermediario; composicion farmaceutica de dicho compuesto; y su uso como antagonista de los receptores de prostaglandina d2 (pgd2) para tratar trastornos inmunologicos, enfermedades alergicas, trastornos inflamatorios.

Info

Publication number
CL2010001528A1
CL2010001528A1 CL2010001528A CL2010001528A CL2010001528A1 CL 2010001528 A1 CL2010001528 A1 CL 2010001528A1 CL 2010001528 A CL2010001528 A CL 2010001528A CL 2010001528 A CL2010001528 A CL 2010001528A CL 2010001528 A1 CL2010001528 A1 CL 2010001528A1
Authority
CL
Chile
Prior art keywords
compound
phenoxychroman
pgd2
prostaglandin
antagonist
Prior art date
Application number
CL2010001528A
Other languages
English (en)
Inventor
Christopher T Clark
Adam Cook
Robert Kirk Delisle
George A Doherty
Kevin W Hunt
Ganghyeok Kim
Todd Romoff
Laurence E Burgess
Christopher P Corrette
Original Assignee
Array Biopharma Inc
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 Array Biopharma Inc filed Critical Array Biopharma Inc
Publication of CL2010001528A1 publication Critical patent/CL2010001528A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/04Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
    • C07D311/58Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/04Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
    • C07D311/06Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2
    • C07D311/20Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2 hydrogenated in the hetero ring
    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/02Nasal agents, e.g. decongestants
    • 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
    • A61P17/00Drugs for dermatological disorders
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/04Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
    • 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
    • C07D405/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D407/00Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/02Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
    • C07D407/12Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

Abstract

COMPUESTOS DE LA FÓRMULA I, E INTERMEDIARIOS DE FÓRMULA LE, VI Y IV, SEGÚN EN DONDE A1, A2, PG, W, L, G, R7A, R7B, R8, R9, R10, P3, P2 Y Z2 TIENEN LAS DEFINICIONES QUE SE DIERON EN LA MEMORIA DESCRIPTIVA, SON MODULADORES DE RECEPTOR DE DP2 QUE SON ÚTILES EN EL TRATAMIENTO DE ENFERMEDADES INMUNOLÓGICAS.
CL2010001528A 2008-06-25 2010-12-23 Compuestos derivados del acido 7-fenoxicroman-4-carboxilico sustituido; proceso de preparacion; compuesto intermediario; composicion farmaceutica de dicho compuesto; y su uso como antagonista de los receptores de prostaglandina d2 (pgd2) para tratar trastornos inmunologicos, enfermedades alergicas, trastornos inflamatorios. CL2010001528A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US7561508P 2008-06-25 2008-06-25

Publications (1)

Publication Number Publication Date
CL2010001528A1 true CL2010001528A1 (es) 2011-07-01

Family

ID=40996727

Family Applications (1)

Application Number Title Priority Date Filing Date
CL2010001528A CL2010001528A1 (es) 2008-06-25 2010-12-23 Compuestos derivados del acido 7-fenoxicroman-4-carboxilico sustituido; proceso de preparacion; compuesto intermediario; composicion farmaceutica de dicho compuesto; y su uso como antagonista de los receptores de prostaglandina d2 (pgd2) para tratar trastornos inmunologicos, enfermedades alergicas, trastornos inflamatorios.

Country Status (33)

Country Link
US (4) US8569522B2 (es)
EP (3) EP2826774B1 (es)
JP (2) JP5753780B2 (es)
KR (1) KR101728175B1 (es)
CN (2) CN103450138B (es)
AR (1) AR072301A1 (es)
AU (1) AU2009262274B2 (es)
BR (1) BRPI0915513B8 (es)
CA (1) CA2729217C (es)
CL (1) CL2010001528A1 (es)
CO (1) CO6362002A2 (es)
CR (1) CR20110037A (es)
CY (1) CY1115650T1 (es)
DK (1) DK2307397T3 (es)
ES (2) ES2524314T3 (es)
HK (1) HK1155735A1 (es)
HR (1) HRP20140988T1 (es)
IL (2) IL210198A (es)
MX (1) MX2011000173A (es)
MY (2) MY185134A (es)
NZ (1) NZ590437A (es)
PH (1) PH12014500079B1 (es)
PL (1) PL2307397T3 (es)
PT (1) PT2307397E (es)
RS (1) RS53665B1 (es)
RU (1) RU2507200C2 (es)
SG (2) SG2014013528A (es)
SI (1) SI2307397T1 (es)
TW (2) TWI436990B (es)
UA (1) UA104867C2 (es)
UY (1) UY31938A (es)
WO (1) WO2009158426A1 (es)
ZA (1) ZA201100604B (es)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ590437A (en) 2008-06-25 2012-07-27 Array Biopharma Inc 6-substituted phenoxychroman carboxylic acid derivatives
US8785445B2 (en) 2008-12-22 2014-07-22 Array Biopharma Inc. 7-phenoxychroman carboxylic acid derivatives
EP2457900A1 (en) 2010-11-25 2012-05-30 Almirall, S.A. New pyrazole derivatives having CRTh2 antagonistic behaviour
TWI654180B (zh) 2012-06-29 2019-03-21 美商艾佛艾姆希公司 殺真菌之雜環羧醯胺
TW201507722A (zh) * 2013-04-30 2015-03-01 Bayer Cropscience Ag 做為殺線蟲劑及殺體內寄生蟲劑的n-(2-鹵素-2-苯乙基)-羧醯胺類
WO2015126750A1 (en) 2014-02-19 2015-08-27 Array Biopharma Inc. BIOMARKERS PREDICTIVE OF RESPONSIVENESS TO TREATMENT WITH A CRTh2 INHIBITOR
CN111057003A (zh) * 2019-12-06 2020-04-24 广安凯特制药有限公司 一种立他司特中间体5,7-二氯-1,2,3,4-四氢异喹啉的合成方法
SE2151519A1 (en) * 2021-12-10 2023-06-11 Amidea Sweden Ab 2-(2,5-dimethoxyphenyl)ethanamine and uses thereof
CN114181039A (zh) * 2021-12-23 2022-03-15 凯美克(上海)医药科技有限公司 一种4,4-二苯基-3-丁烯-1-醇的合成方法

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5059609A (en) 1987-10-19 1991-10-22 Pfizer Inc. Substituted tetralins, chromans and related compounds in the treatment of asthma, arthritis and related diseases
US5006550A (en) * 1989-12-29 1991-04-09 Allergan, Inc. Chroman esters of phenols and benzoic acids having retinoid-like activity
US5952326A (en) 1997-12-10 1999-09-14 Pfizer Inc. Tetralin and chroman derivatives useful in the treatment of asthma, arthritis and related diseases
DE19850131A1 (de) * 1998-10-30 2000-05-04 Merck Patent Gmbh Chromenon- und Chromanonderivate
IL145949A0 (en) 1999-05-21 2002-07-25 Pfizer Prod Inc 1-trifluoromethyl-4-hydroxy-7-piperidinyl-aminomethylchroman derivatives
US7855297B2 (en) * 2000-09-14 2010-12-21 Mitsubishi Tanabe Pharma Corporation Amide derivatives and medicinal use thereof
WO2003029239A1 (en) * 2001-10-04 2003-04-10 Wyeth Chroman and benzofuran derivatives as 5-hydroxytryptamine-6 ligands
KR20050111314A (ko) * 2002-12-20 2005-11-24 암젠 인코포레이션 천식 및 알레르기성 염증 조절제들
EP1856040A4 (en) * 2005-02-25 2009-09-23 Lilly Co Eli NEW LIPOXYGENASE INHIBITORS
GB0611781D0 (en) * 2006-06-14 2006-07-26 Argenta Discovery Ltd 2-Oxo-2H-Chromene Compounds
KR101397352B1 (ko) * 2006-08-21 2014-05-19 어레이 바이오파마 인크. 4-치환된 페녹시페닐아세트산 유도체
AU2007314405A1 (en) * 2006-10-31 2008-05-08 Merck & Co., Inc. Antidiabetic bicyclic compounds
US7960567B2 (en) * 2007-05-02 2011-06-14 Amgen Inc. Compounds and methods useful for treating asthma and allergic inflammation
US8362056B2 (en) * 2007-11-05 2013-01-29 Array Biopharma Inc. 4-heteroaryl-substituted phenoxyphenylacetic acid derivatives
NZ590437A (en) 2008-06-25 2012-07-27 Array Biopharma Inc 6-substituted phenoxychroman carboxylic acid derivatives
US8785445B2 (en) * 2008-12-22 2014-07-22 Array Biopharma Inc. 7-phenoxychroman carboxylic acid derivatives

Also Published As

Publication number Publication date
US8569522B2 (en) 2013-10-29
EP3144303A1 (en) 2017-03-22
PH12014500079A1 (en) 2015-02-09
CR20110037A (es) 2011-03-14
US8716498B2 (en) 2014-05-06
RU2011102595A (ru) 2012-07-27
EP3144303B1 (en) 2018-09-26
KR101728175B1 (ko) 2017-04-18
IL210198A (en) 2015-10-29
EP2307397B1 (en) 2014-08-20
CN102131794A (zh) 2011-07-20
AR072301A1 (es) 2010-08-18
BRPI0915513B1 (pt) 2019-11-19
ES2524314T3 (es) 2014-12-05
CN102131794B (zh) 2013-09-25
PL2307397T3 (pl) 2015-02-27
DK2307397T3 (da) 2014-11-03
US9096567B2 (en) 2015-08-04
IL241754A (en) 2017-02-28
US20140005418A1 (en) 2014-01-02
PH12014500079B1 (en) 2015-02-09
TWI436990B (zh) 2014-05-11
WO2009158426A1 (en) 2009-12-30
ES2582161T3 (es) 2016-09-09
CN103450138A (zh) 2013-12-18
TWI476186B (zh) 2015-03-11
CN103450138B (zh) 2015-04-08
US20140221342A1 (en) 2014-08-07
US20150232442A1 (en) 2015-08-20
RU2507200C2 (ru) 2014-02-20
HRP20140988T1 (hr) 2014-12-05
CA2729217A1 (en) 2009-12-30
MX2011000173A (es) 2011-06-20
TW201022222A (en) 2010-06-16
SI2307397T1 (sl) 2014-11-28
AU2009262274B2 (en) 2013-08-01
HK1155735A1 (en) 2012-05-25
RS53665B1 (en) 2015-04-30
EP2307397A1 (en) 2011-04-13
EP2826774B1 (en) 2016-05-25
US20110105463A1 (en) 2011-05-05
BRPI0915513A2 (pt) 2016-01-26
ZA201100604B (en) 2015-08-26
UY31938A (es) 2011-01-31
MY161425A (en) 2017-04-14
CY1115650T1 (el) 2017-01-04
NZ590437A (en) 2012-07-27
KR20110027798A (ko) 2011-03-16
SG2014013544A (en) 2014-07-30
JP5753780B2 (ja) 2015-07-22
EP2826774A1 (en) 2015-01-21
BRPI0915513B8 (pt) 2021-05-25
US9556139B2 (en) 2017-01-31
CA2729217C (en) 2016-09-06
IL241754A0 (en) 2015-11-30
SG2014013528A (en) 2014-07-30
PT2307397E (pt) 2014-10-29
JP2014122241A (ja) 2014-07-03
TW201427965A (zh) 2014-07-16
IL210198A0 (en) 2011-03-31
UA104867C2 (uk) 2014-03-25
MY185134A (en) 2021-04-30
JP2011526290A (ja) 2011-10-06
AU2009262274A1 (en) 2009-12-30
CO6362002A2 (es) 2012-01-20

Similar Documents

Publication Publication Date Title
CL2010001528A1 (es) Compuestos derivados del acido 7-fenoxicroman-4-carboxilico sustituido; proceso de preparacion; compuesto intermediario; composicion farmaceutica de dicho compuesto; y su uso como antagonista de los receptores de prostaglandina d2 (pgd2) para tratar trastornos inmunologicos, enfermedades alergicas, trastornos inflamatorios.
CR11174A (es) Composicion, metodo y preparacion del acido biliar sintetico
DOP2014000115A (es) Uso de 4-fenil-piridinas sustituidas para la fabricación de medicamentos útiles en el tratamiento de enfermedades relacionadas con el receptor de nk1
BR112015012555A2 (pt) derivados de benzimidazol como antagonistas de ep4
EA200970835A1 (ru) Индазолы, применяемые для лечения расстройств, опосредуемых эстрогеновым рецептором бета
CO6480918A2 (es) Antagonistas policíclicos de receptores de ácido lisofosfatídico.
ECSP10010209A (es) Agonistas novedosos de los receptores de glucocorticoides
EA201201343A1 (ru) Производные 4-аминопиримидина и их действующее вещество как антагонисты аденозинового рецептора а
EA201290940A1 (ru) Новые соединения как селективные антагонисты рецептора nk3, фармацевтическая композиция и методы их использования при нарушениях, опосредованных nk3 рецепторами
ECSP11010754A (es) Derivados de triazol útiles para el tratamiento de enfermedades
BR112013001088A2 (pt) "derivados substituídos como inibidores a quinase de imidazoquinolina"
DOP2013000105A (es) Derivados de 2,3-dihidroimidazo[1,2-c]quinazolina sustituidos con aminoalcoholes que son de utilidad para tratar trastornos hiperproliferativos y enfermedades asociadas a la angiogénesis
NI201100084A (es) Antagonistas del receptor de orexina de isonicotinamida.
EA201501122A1 (ru) Новые агонисты соматостатиновых рецепторов подтипа 4 (sstr4)
CO6640327A2 (es) Compuestos de pirazol como inhibidores del receptor sigma
EA201291038A1 (ru) Соединения пиразола в качестве ингибиторов jak
CO6852073A2 (es) Antagonistas trpm8 y su uso en tratamientos
NI201300043A (es) Antagonistas del receptor del cgrp de piperidinona carboxamida azaindano
CL2008003811A1 (es) Compuestos derivados de 4-aminopirimidina-2,6-disustituidos, antagonistas del receptor de histamina h4; proceso de preparacion; composicion farmaceutica que comprende a dicho compuesto; y uso del compuesto para el tratamiento de una enfermedad alergica, inmunologica o inflamatoria, o dolor.
UY35906A (es) Novedosos derivados de bencimidazol como ligandos de ep4
CR20140257A (es) Nuevos 2h-indazoles como antagonistas del receptor ep2
CU24365B1 (es) Derivados de oxazolidin-2-ona-pirimidina
DOP2010000232A (es) Derivados de indazol
MX2011012669A (es) Nuevos agonistas del receptor de glucocorticoides.
EA200602049A1 (ru) Пролекарства стероидов с андрогенным действием