AR037330A1 - Derivado de quinazolina, composicion farmaceutica, su uso en la fabricacion de un medicamento y proceso para preparar dicho derivado de quinazolina - Google Patents

Derivado de quinazolina, composicion farmaceutica, su uso en la fabricacion de un medicamento y proceso para preparar dicho derivado de quinazolina

Info

Publication number
AR037330A1
AR037330A1 ARP020104181A ARP020104181A AR037330A1 AR 037330 A1 AR037330 A1 AR 037330A1 AR P020104181 A ARP020104181 A AR P020104181A AR P020104181 A ARP020104181 A AR P020104181A AR 037330 A1 AR037330 A1 AR 037330A1
Authority
AR
Argentina
Prior art keywords
alkyl
amino
group
carbamoyl
heterocyclyl
Prior art date
Application number
ARP020104181A
Other languages
English (en)
Inventor
Laurent Hennequin
Jason Kettle
Martin Pass
Robert Bradbury
Original Assignee
Astrazeneca Ab
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 GBGB0126433.2A external-priority patent/GB0126433D0/en
Priority claimed from GB0129059A external-priority patent/GB0129059D0/en
Application filed by Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of AR037330A1 publication Critical patent/AR037330A1/es

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/12—Heterocyclic 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/08—Drugs for disorders of the urinary system of the prostate
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/10—Drugs for disorders of the urinary system of the bladder
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/06—Antipsoriatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/08—Vasodilators for multiple indications
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72—Quinazolines; Hydrogenated quinazolines
    • C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
    • C07D239/94—Nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/14—Heterocyclic 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 three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic 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
    • C07D403/12—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic 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
    • C07D405/14—Heterocyclic 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 three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Urology & Nephrology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Dermatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Un derivado de quinazolina que responde a la fórmula (1), donde: R1 es hidrógeno o alquilo (C1-6); Z es un enlace directo o se selecciona entre O, S y N(R2), donde R2 es hidrógeno o alquilo (C1-6); Q1 es cicloalquilo (C3-7), cicloalquil (C3-7)-alquilo (C1-6), cicloalquelino (C3-7), cicloalquenil (C3-7)-alquilo (C1-6), heterociclilo o heterociclil-alquilo (C1-6), y donde los átomos de carbono adyacentes en cualquier cadena alquileno (C2-6) dentro del grupo Q1-Z- se separan opcionalmente por la inserción en la cadena de un grupo seleccionado entre O, S, SO, SO2, N(R3), CO, CH(OR3), CON(R3), N(R3)CO, SO2N(R3), N(R3)SO2, CH=CH y CsC donde R3 es hidrógeno o alquilo (C1-6), y donde cualquier grupo CH2 o CH3 dentro del grupo Q1-Z- opcionalmente lleva en cada uno de los dichos grupos CH2 o CH3 uno o más sustituyentes halógeno o alquilo (C1-6) o un sustituyente seleccionado entre hidroxi, ciano, amino, carboxi, carbamoilo, alcoxi (C1-6), alquiltio (C1-6), alquilsulfinilo (C1-6), alquilsulfonilo (C1-6), alquilamino (C1-6), di-[alquil (C1-6)]amino, alcoxicarbonilo (C1-6), N-alquilcarbamoilo (C1-6), N,N-di-[alquil (C1-6)]carbamoilo, alcanoilo (C2-6), alcanoiloxi (C2-6), alcanoilamino (C2-6), N-alquil (C1-6)-alcanoilamino (C2-6), N-alquilsulfamoilo (C1-6), N,N-di-[alquil (C1-6)]sulfamoilo, alcansulfonilamino (C1-6) y N-alquil (C1-6)-alcansulfonilamino (C1-6), y donde cualquier grupo heterociclilo, cicloalquilo (C3-7) o cicloalquelino (C3-7) dentro del grupo Q1-Z- opcionalmente lleva 1, 2 ó 3 sustituyentes, que pueden ser iguales o diferentes, seleccionados entre halógeno, trifluorometilo, ciano, nitro, hidroxi, amino, carboxi, carbamoilo, formilo, alquilo (C1-6), alquenilo (C2-8), alquinilo (C2-8), alcoxi (C1-6), alqueniloxi (C2-6), alquiniloxi (C2-6), alquiltio (C1-6), alquilsulfinilo (C1-6), alquilsulfonilo (C1-6), alquilamino (C1-6), di-[alquil (C1-6)]amino, alcoxicarbonilo (C1-6), N-alquilcarbamoilo (C1-6), N,N-di-[alquil (C1-6)]carbamoilo, alcanoilo (C2-6), alcanoiloxi (C2-6), amino-alcanoilo (C2-6), N-alquilamino (C1-6)-alcanoilo (C2-6), N,N-di-[alquil (C1-6)]amino-alcanoilo (C2-6), alcanoilamino (C2-6), N-alquil (C1-6)-alcanoilamino (C2-6), N-alquilsulfamoilo (C1-6), N,N-di-[alquil (C1-6)]sulfamoilo, alcansulfonilamino (C1-6), N-alquil (C1-6)-alcansulfonilamino (C1-6), de un grupo de la fórmula: -X1-R4, donde X1 es un enlace, directo o se selecciona entre O y N(R5), donde R5 es hidrógeno o alquilo (C1-6), y R4 es halógeno-alquilo (C1-6), hidroxi-alquilo (C1-6), alcoxi (C1-6)-alquilo (C1-6), ciano-alquilo (C1-6), carboxi-alquilo (C1-6), amino-alquilo (C1-6), alquilamino (C1-6)-alquilo (C1-6), di-[alquil (C1-6)]amino-alquilo (C1-6), carbamoil-alquilo (C1-6), N-alquilcarbonil (C1-6)-alquilo (C1-6), N,N-di-[alquil (C1-6)]carbamoil-alquilo (C1-6), alcanoil (C2-6)-alquilo (C1-6) o alcoxicarbonil (C1-6)-alquilo (C1-6), y un grupo de la fórmula: -X5-Q6 donde X5 es un enlace directo o se selecciona entre O, CO, y N(R10), donde R10 es hidrógeno o alquilo (C1-6), y Q6 es heterociclilo, heterociclil-alquilo (C1-6), cicloalquilo (C3-7), cicloalquil (C3-7)-alquilo (C1-6), cicloalquenilo (C3-7) o cicloalquenil (C3-7)-alquilo (C1-6), y en donde cualquier grupo heterociclilo, cicloalquilo (C3-7) o cicloalquenilo (C3-7) en Q6 opcionalmente lleva 1 ó 2 sustituyentes, que pueden ser iguales o diferentes, seleccionados entre halógeno, hidroxi, ciano, formilo, alquilo (C1-6), alquenilo (C2-6), alquinilo (C2-6), alcoxi (C1-6), amino, alquilamino (C1-6), di[alquil (C1-6)]amino, alcanoilo (C2-6), alcoxicarbonilo (C1-6), alquilsulfinilo (C1-6), carbamoilo, N-(C1-6)alquilcarbamoilo, N,N-di-[alquil (C1-6)]carbamoilo, halógeno-alquilo (C1-6), hidroxi-alquilo (C1-6), alcoxi (C1-6)-alquilo (C1-6), ciano-alquilo (C1-6), carboxi-alquilo (C1-6), amino-alquilo (C1-6), alquilamino (C1-6)-alquilo (C1-6), di-[alquil (C1-6)]amino-alquilo (C1-6), carbamoil-alquilo (C1-6), N-alquilcarbamoil (C1-6)-alquilo (C1-6) y N,N-di-[alquil (C1-6)]carbamoil-alquilo (C1-6), y donde cualquier grupo heterociclilo dentro del grupo Q1-Z- opcionalmente lleva 1 ó 2 sustituyentes oxo o tioxo; y Q2 se selecciona entre el grupo de fórmulas (2), donde G1, G2, G3, G4 y G5 son cada uno, independientemente, seleccionado entre hidrógeno, halógeno, trifluorometilo, ciano, nitro, hidroxi, amino, carboxi, carbamoilo, alquilo (C1-6), alquenilo (C2-8), alquinilo (C2-8), alcoxi (C1-6), alqueniloxi (C2-6), alquiniloxi (C2-6), alquilamino (C1-6) y di-[alquil (C1-6)]amino, G6 y G7 son cada uno, independientemente, seleccionado entre hidrógeno y halógeno, X2 es un enlace directo o se selecciona entre O, S, SO, SO2, N(R6), CH(OR6), CON(R6), N(R6)CO, SO2N(R6), N(R6)SO2, OC(R6)2, C(R6)2O, SC(R6)2, C(R6)2S, CO, C(R6)2N(R6) y N(R6)C(R6)2 donde cada R6 es, independientemente, hidrógeno o alquilo (C1-6), y Q3 es arilo, o heteroarilo, o X2 es CO y Q3 es un grupo heterociclilo con contenido de nitrógeno unido a X2 por un átomo de nitrógeno, X3 es un enlace directo o se selecciona entre SO2, CO, SO2N(R) y C(R7)2, donde cada R7 es, independientemente, hidrógeno o alquilo (C1-6), y Q4 es arilo o heteroarilo, y cualquier grupo arilo, heteroarilo o heterociclilo en el grupo -X2-Q3 y -X3-Q4 opcionalmente lleva 1, 2 ó 3 sustituyentes, que pueden ser iguales o diferentes, seleccionados entre halógeno, trifluorometilo, ciano, nitro, hidroxi, amino, carboxi, formilo, carbamoilo, sulfamoilo, mercapto, alquilo (C1-6), alquenilo (C2-8), alquinilo (C2-8), alcoxi (C1-6), alqueniloxi (C2-6), alquiniloxi (C2-6), alquiltio (C1-6), alquilsulfinilo (C1-6), alquilsulfonilo (C1-6), alquilamino (C1-6), di-[alquil (C1-6)]amino, alcoxicarbonilo (C1-6), N-alquilcarbamoilo (C1-6), N,N-di-[alquil(C1-6)]carbamoilo, alcanoilo (C2-6), alcanoiloxi (C2-6), alcanoilamino (C2-6), N-alquil (C1-6)-alcanoilamino (C2-6), N-alquilsulfamoilo (C1-6), N,N-di-[alquil(C1-6)]sulfamoilo, alcansulfonilamino (C1-6) y N-alquil (C1-6)-alcansulfonilamino (C1-6), o es un grupo de la fórmula X4-R8 donde X4 es un enlace directo o se selecciona entre O y N(R9), donde R9 es hidrógeno o alquilo (C1-6), y R8 es halógeno-alquilo (C1-6), hidroxi-alquilo (C1-6), alcoxi-alquilo (C1-6), ciano-alquilo (C1-6), carboxi-alquilo (C1-6), amino-alquilo (C1-6), alquilamino (C1-6)-alquilo (C1-6), di-[alquil (C1-6)]amino-alquilo (C1-6), carbamoilo-alquilo (C1-6), N-alquilcarbamoil (C1-6)-alquilo (C1-6), N,N-di-[alquil (C1-6)]carbamoil-alquilo (C1-6), alcanoil (C2-6)-alquilo (C1-6) o alcoxicarbonil (C1-6)-alquilo (C1-6), o es un grupo de la fórmula -Q5 donde Q5 se selecciona entre arilo, heteroarilo o heterociclilo que es opcionalmente sustituido por 1 ó 2 sustituyentes seleccionados entre halógeno, hidroxi, alquilo (C1-6), alcoxi (C1-6), amino, alquilamino (C1-6) y di-[alquil(C1-6)]amino, y donde cualquier grupo CH2 o CH3 dentro de un sustituyente en cualquier grupo arilo, heteroarilo o heterociclilo en el grupo -X2-Q3 y -X3-Q4 opcionalmente lleva en cada uno de dichos grupos CH2 o CH3 uno o más sustituyentes halógeno o alquilo (C1-6), y cualquier grupo heterociclilo representado por Q3 o Q4 opcionalmente lleva 1 ó 2 sustituyentes oxo o tioxo, o una sal aceptable para uso farmacéutico del mismo. Los procesos para su preparación, composiciones farmacéuticas que los contienen y su uso en la fabricación de un medicamento para usar en la prevención o tratamiento de tumores que son sensibles a la inhibición de miembros de la familia erbB de tirosina quinasas de receptor, también se describen.
ARP020104181A 2001-11-03 2002-11-01 Derivado de quinazolina, composicion farmaceutica, su uso en la fabricacion de un medicamento y proceso para preparar dicho derivado de quinazolina AR037330A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB0126433.2A GB0126433D0 (en) 2001-11-03 2001-11-03 Compounds
GB0129059A GB0129059D0 (en) 2001-12-05 2001-12-05 Compounds

Publications (1)

Publication Number Publication Date
AR037330A1 true AR037330A1 (es) 2004-11-03

Family

ID=26246737

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Application Number Title Priority Date Filing Date
ARP020104181A AR037330A1 (es) 2001-11-03 2002-11-01 Derivado de quinazolina, composicion farmaceutica, su uso en la fabricacion de un medicamento y proceso para preparar dicho derivado de quinazolina

Country Status (23)

Country Link
US (2) US20050043336A1 (es)
EP (1) EP1444210B1 (es)
JP (1) JP2005515176A (es)
KR (1) KR20050042055A (es)
CN (1) CN100343238C (es)
AR (1) AR037330A1 (es)
AT (1) ATE423104T1 (es)
BR (1) BR0213842A (es)
CA (1) CA2465068A1 (es)
CO (1) CO5580774A2 (es)
DE (1) DE60231230D1 (es)
ES (1) ES2320980T3 (es)
HK (1) HK1066218A1 (es)
HU (1) HUP0401646A2 (es)
IL (1) IL161619A0 (es)
IS (1) IS7240A (es)
MX (1) MXPA04004219A (es)
NO (1) NO20042279L (es)
NZ (1) NZ532524A (es)
PL (1) PL369938A1 (es)
RU (1) RU2004116911A (es)
TW (1) TW200301702A (es)
WO (1) WO2003040108A1 (es)

Families Citing this family (75)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2441492C (en) * 2001-03-23 2011-08-09 Bayer Corporation Rho-kinase inhibitors
MY142915A (en) * 2001-03-23 2011-01-31 Bayer Healthcare Llc Rho-kinase inhibitors
GB0126433D0 (en) * 2001-11-03 2002-01-02 Astrazeneca Ab Compounds
KR101093345B1 (ko) * 2002-02-01 2011-12-14 아스트라제네카 아베 퀴나졸린 화합물
US6924285B2 (en) 2002-03-30 2005-08-02 Boehringer Ingelheim Pharma Gmbh & Co. Bicyclic heterocyclic compounds, pharmaceutical compositions containing these compounds, their use and process for preparing them
US7488823B2 (en) * 2003-11-10 2009-02-10 Array Biopharma, Inc. Cyanoguanidines and cyanoamidines as ErbB2 and EGFR inhibitors
AU2003292435A1 (en) * 2002-12-23 2004-07-14 Astrazeneca Ab 4- (pyridin-4-ylamino) -quinazoline derivatives as anti-tumor agents
TW200503994A (en) * 2003-01-24 2005-02-01 Novartis Ag Organic compounds
GB0309009D0 (en) * 2003-04-22 2003-05-28 Astrazeneca Ab Quinazoline derivatives
GB0309850D0 (en) * 2003-04-30 2003-06-04 Astrazeneca Ab Quinazoline derivatives
WO2004106308A1 (en) * 2003-05-27 2004-12-09 Pfizer Products Inc. Quinazolines and pyrido [3,4-d] pyrimidines as receptor tyrosine kinase inhibitors
AU2004256124B2 (en) * 2003-07-02 2011-04-28 Corus Pharma, Inc. Aztreonam L-lysine and methods for the preparation thereof
US8309562B2 (en) 2003-07-03 2012-11-13 Myrexis, Inc. Compounds and therapeutical use thereof
GB0317665D0 (en) 2003-07-29 2003-09-03 Astrazeneca Ab Qinazoline derivatives
PT1660090E (pt) * 2003-08-14 2013-01-11 Array Biopharma Inc Análogos de quinazolina como inibidores de tirosina-cinases recetoras
US7501427B2 (en) 2003-08-14 2009-03-10 Array Biopharma, Inc. Quinazoline analogs as receptor tyrosine kinase inhibitors
KR20070027487A (ko) * 2003-09-16 2007-03-09 아스트라제네카 아베 퀴나졸린 유도체
WO2005026156A1 (en) * 2003-09-16 2005-03-24 Astrazeneca Ab Quinazoline derivatives
JP2007505873A (ja) * 2003-09-16 2007-03-15 アストラゼネカ アクチボラグ チロシンキナーゼ阻害剤としてのキナゾリン誘導体
CA2538884C (en) * 2003-09-16 2010-09-21 Astrazeneca Ab Quinazoline derivatives as tyrosine kinase inhibitors
GB0321648D0 (en) * 2003-09-16 2003-10-15 Astrazeneca Ab Quinazoline derivatives
GB0322409D0 (en) * 2003-09-25 2003-10-29 Astrazeneca Ab Quinazoline derivatives
GB0326459D0 (en) * 2003-11-13 2003-12-17 Astrazeneca Ab Quinazoline derivatives
US20050171172A1 (en) * 2003-11-13 2005-08-04 Ambit Biosciences Corporation Amide derivatives as PDGFR modulators
KR20170102377A (ko) 2004-01-22 2017-09-08 유니버시티 오브 마이애미 국소용 코-엔자임 큐10 제형 및 그의 사용 방법
EP1711495A2 (en) 2004-01-23 2006-10-18 Amgen Inc. Quinoline, quinazoline, pyridine and pyrimidine counds and their use in the treatment of inflammation, angiogenesis and cancer
AU2005206571B8 (en) 2004-01-23 2010-09-02 Amgen Inc. Compounds and methods of use
WO2005075439A1 (en) * 2004-02-03 2005-08-18 Astrazeneca Ab Quinazoline derivatives
FR2866887A1 (fr) * 2004-02-27 2005-09-02 Oreal Para-phenylenediamine secondaire n-heteroaryle, compositon tinctoriale comprenant une telle para-phenylenediamine, procede mettant en oeuvre cette composition et utilisation
PT1746999E (pt) 2004-05-06 2012-01-11 Warner Lambert Co 4-fenilamino-quinazolin-6-il-amidas
US20070232607A1 (en) * 2004-06-04 2007-10-04 Bradbury Robert H Quinazoline Derivatives as Erbb Receptor Tyrosine kinases
JP2008513463A (ja) 2004-09-15 2008-05-01 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ チアゾロピリジンキナーゼ阻害剤
ATE540935T1 (de) 2004-10-12 2012-01-15 Astrazeneca Ab Chinazolinderivate
EP1827434B1 (en) 2004-11-30 2014-01-15 Amgen Inc. Quinolines and quinazoline analogs and their use as medicaments for treating cancer
EP1828152B1 (en) * 2004-12-08 2008-08-20 Bristol-Myers Squibb Company Heterocyclic compounds as inhibitors of factor viia
JP4881875B2 (ja) * 2004-12-14 2012-02-22 アストラゼネカ アクチボラグ 抗腫瘍剤としてのピラゾロピリミジン化合物
US8258145B2 (en) 2005-01-03 2012-09-04 Myrexis, Inc. Method of treating brain cancer
CA2592900A1 (en) 2005-01-03 2006-07-13 Myriad Genetics Inc. Nitrogen containing bicyclic compounds and therapeutical use thereof
WO2006081741A1 (fr) * 2005-02-05 2006-08-10 Piaoyang Sun Dérivés de quinazoline ou leurs sels de qualité pharmaceutique, synthèse et applications médicales desdites substances
GB0504475D0 (en) * 2005-03-04 2005-04-13 Astrazeneca Ab Chemical compounds
GB0504474D0 (en) * 2005-03-04 2005-04-13 Astrazeneca Ab Chemical compounds
JO2787B1 (en) 2005-04-27 2014-03-15 امجين إنك, Alternative amide derivatives and methods of use
GB0508717D0 (en) * 2005-04-29 2005-06-08 Astrazeneca Ab Chemical compounds
GB0508715D0 (en) * 2005-04-29 2005-06-08 Astrazeneca Ab Chemical compounds
US7579356B2 (en) * 2005-05-04 2009-08-25 Janssen Pharmaceutica Nv Thia-tetraazaacenaphthylene kinase inhibitors
WO2007034144A1 (en) * 2005-09-20 2007-03-29 Astrazeneca Ab 4- (ih-indazol-s-yl-amino)-quinazoline compounds as erbb receptor tyrosine kinase inhibitors for the treatment of cancer
WO2007034143A1 (en) * 2005-09-20 2007-03-29 Astrazeneca Ab Quinazoline derivatives as anticancer agents
CA2632194C (en) * 2005-11-15 2012-01-03 Array Biopharma Inc. N4-phenyl-quinazoline-4-amine derivatives and related compounds as erbb type i receptor tyrosine kinase inhibitors for the treatment of hyperproliferative diseases
JP2009517451A (ja) * 2005-12-02 2009-04-30 アストラゼネカ アクチボラグ Ｅｒｂｂチロシンキナーゼの阻害剤として使用されるキナゾリン誘導体
US20100222344A1 (en) * 2005-12-02 2010-09-02 Astrazeneca Ab 4-anilino-substituted quinazoline derivatives as tyrosine kinase inhibitors
UY30183A1 (es) 2006-03-02 2007-10-31 Astrazeneca Ab Derivados de quinolina
JP2009544609A (ja) * 2006-07-18 2009-12-17 アストラゼネカ・アクチエボラーグ 置換２−アセチルアミノ−アルコキシフェニルの製造方法
EP1921070A1 (de) 2006-11-10 2008-05-14 Boehringer Ingelheim Pharma GmbH & Co. KG Bicyclische Heterocyclen, diese Verbindungen enthaltende Arzneimittel, deren Verwendung und Verfahren zu ihrer Herstelllung
FR2912145B1 (fr) * 2007-02-02 2009-03-06 Servier Lab Nouveaux derives tricycliques,leur procede de preparation et les compositions pharmaceutiques qui les contiennent
JP5377332B2 (ja) 2007-02-06 2013-12-25 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 二環式へテロ環、それらの化合物を含む薬剤、その使用及びその製法
ES2470341T3 (es) * 2007-04-05 2014-06-23 Amgen, Inc Moduladores de la aurora cinasa y método de uso
MY150054A (en) 2007-10-29 2013-11-29 Natco Pharma Ltd Novel 4-(tetrazol-5-yl)-quinazoline derivatives as anti cancer agents
AU2008319366B2 (en) * 2007-10-29 2012-03-01 Amgen Inc. Benzomorpholine derivatives and methods of use
EA019709B1 (ru) 2008-02-07 2014-05-30 Бёрингер Ингельхайм Интернациональ Гмбх Спирогетероциклы и их применение в качестве лекарственных средств
WO2009126764A1 (en) 2008-04-11 2009-10-15 Cytotech Labs, Llc Methods and use of inducing apoptosis in cancer cells
CA2723989C (en) 2008-05-13 2017-04-25 Astrazeneca Ab Fumarate salt of 4-(3-chloro-2-fluoroanilino)-7-methoxy-6-{[1-(n-methylcarbamoylmethyl)piperidin-4-yl]oxy}quinazoline
CA2733153C (en) 2008-08-08 2016-11-08 Boehringer Ingelheim International Gmbh Cyclohexyloxy substituted heterocycles, pharmaceutical compositions containing these compounds and processes for preparing them
WO2010132502A2 (en) 2009-05-11 2010-11-18 Cytotech Labs, Llc Methods for treatment of metabolic disorders using epimetabolic shifters, multidimensional intracellular molecules, or environmental influencers
AU2012240222B2 (en) 2011-04-04 2017-04-27 Berg Llc Methods of treating central nervous system tumors
US10933032B2 (en) 2013-04-08 2021-03-02 Berg Llc Methods for the treatment of cancer using coenzyme Q10 combination therapies
EP3730131A1 (en) 2013-09-04 2020-10-28 Berg LLC Methods of treatment of cancer by continuous infusion of coenzyme q10
EP3071204B1 (en) 2013-11-20 2019-02-20 SignalChem Lifesciences Corp. Quinazoline derivatives as tam family kinase inhibitors
WO2016021742A1 (en) 2014-08-07 2016-02-11 Takeda Pharmaceutical Company Limited Heterocyclic compounds as ep4 receptor antagonists
CN106831599B (zh) * 2017-03-03 2019-08-23 南京理工大学 一种合成1-二氟甲基咪唑及其衍生物的方法
CN107400094B (zh) * 2017-09-08 2020-04-03 贾玉庆 喹唑啉基羧酸酯类化合物及其用途
CN108285421A (zh) * 2018-01-26 2018-07-17 黑龙江鑫创生物科技开发有限公司 一种微通道反应器合成拉帕替尼中间体的方法
TWI811358B (zh) * 2018-05-08 2023-08-11 大陸商迪哲（江蘇）醫藥股份有限公司 ＥｒｂＢ受體抑制劑
AU2019341273A1 (en) * 2018-09-18 2020-11-19 F. Hoffmann-La Roche Ag Quinazoline derivatives as antitumor agents
CN109336828B (zh) * 2018-11-30 2022-04-26 雅安职业技术学院 一种喹唑啉衍生物及其制备方法和应用
CN113200945A (zh) * 2021-04-23 2021-08-03 上海应用技术大学 一种芳香胺化合物的制备方法

Family Cites Families (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5538325A (en) * 1978-09-11 1980-03-17 Sankyo Co Ltd 4-anilinoquinazoline derivative and its preparation
GB2160201B (en) * 1984-06-14 1988-05-11 Wyeth John & Brother Ltd Quinazoline and cinnoline derivatives
CA1340821C (en) * 1988-10-06 1999-11-16 Nobuyuki Fukazawa Heterocyclic compounds and anticancer-drug reinforcing agents containing them as effective components
US5721237A (en) * 1991-05-10 1998-02-24 Rhone-Poulenc Rorer Pharmaceuticals Inc. Protein tyrosine kinase aryl and heteroaryl quinazoline compounds having selective inhibition of HER-2 autophosphorylation properties
GB9510757D0 (en) * 1994-09-19 1995-07-19 Wellcome Found Therapeuticaly active compounds
TW321649B (es) * 1994-11-12 1997-12-01 Zeneca Ltd
US5747498A (en) * 1996-05-28 1998-05-05 Pfizer Inc. Alkynyl and azido-substituted 4-anilinoquinazolines
US6046206A (en) * 1995-06-07 2000-04-04 Cell Pathways, Inc. Method of treating a patient having a precancerous lesions with amide quinazoline derivatives
GB9514265D0 (en) * 1995-07-13 1995-09-13 Wellcome Found Hetrocyclic compounds
GB9624482D0 (en) * 1995-12-18 1997-01-15 Zeneca Phaema S A Chemical compounds
ES2237789T3 (es) * 1996-01-31 2005-08-01 Cosmoferm B.V. Utilizacion de composiciones que comprenden enzimas estabilizantes.
GB9603095D0 (en) * 1996-02-14 1996-04-10 Zeneca Ltd Quinazoline derivatives
AU3766897A (en) * 1996-07-13 1998-02-09 Glaxo Group Limited Fused heterocyclic compounds as protein tyrosine kinase inhibitors
US6004967A (en) * 1996-09-13 1999-12-21 Sugen, Inc. Psoriasis treatment with quinazoline compounds
AR012634A1 (es) * 1997-05-02 2000-11-08 Sugen Inc Compuesto basado en quinazolina, composicion famaceutica que lo comprende, metodo para sintetizarlo, su uso, metodos de modulacion de la funcion deserina/treonina proteinaquinasa con dicho compuesto y metodo in vitro para identificar compuestos que modulan dicha funcion
US5929080A (en) * 1997-05-06 1999-07-27 American Cyanamid Company Method of treating polycystic kidney disease
US6384223B1 (en) * 1998-07-30 2002-05-07 American Home Products Corporation Substituted quinazoline derivatives
UA71945C2 (en) * 1999-01-27 2005-01-17 Pfizer Prod Inc Substituted bicyclic derivatives being used as anticancer agents
US6080747A (en) * 1999-03-05 2000-06-27 Hughes Institute JAK-3 inhibitors for treating allergic disorders
UA73993C2 (uk) * 2000-06-06 2005-10-17 Астразенека Аб Хіназолінові похідні для лікування пухлин та фармацевтична композиція
EP1578722A4 (en) * 2001-10-12 2006-09-06 Irm Llc KINASEINHIBITOR SCAFFOLD AND METHOD FOR THE PRODUCTION THEREOF
GB0126433D0 (en) * 2001-11-03 2002-01-02 Astrazeneca Ab Compounds
TW200813014A (en) * 2002-03-28 2008-03-16 Astrazeneca Ab Quinazoline derivatives
US6924285B2 (en) * 2002-03-30 2005-08-02 Boehringer Ingelheim Pharma Gmbh & Co. Bicyclic heterocyclic compounds, pharmaceutical compositions containing these compounds, their use and process for preparing them
GB0309009D0 (en) * 2003-04-22 2003-05-28 Astrazeneca Ab Quinazoline derivatives
GB0309850D0 (en) * 2003-04-30 2003-06-04 Astrazeneca Ab Quinazoline derivatives
GB0317665D0 (en) * 2003-07-29 2003-09-03 Astrazeneca Ab Qinazoline derivatives
WO2005012290A1 (en) * 2003-07-29 2005-02-10 Astrazeneca Ab Piperidyl-quinazoline derivatives as tyrosine kinase inhibitors
JP2007505873A (ja) * 2003-09-16 2007-03-15 アストラゼネカ アクチボラグ チロシンキナーゼ阻害剤としてのキナゾリン誘導体
CA2538884C (en) * 2003-09-16 2010-09-21 Astrazeneca Ab Quinazoline derivatives as tyrosine kinase inhibitors
GB0321648D0 (en) * 2003-09-16 2003-10-15 Astrazeneca Ab Quinazoline derivatives
KR20070027487A (ko) * 2003-09-16 2007-03-09 아스트라제네카 아베 퀴나졸린 유도체
JP2007505878A (ja) * 2003-09-19 2007-03-15 アストラゼネカ アクチボラグ キナゾリン誘導体
GB0322409D0 (en) * 2003-09-25 2003-10-29 Astrazeneca Ab Quinazoline derivatives
BRPI0414735A (pt) * 2003-09-25 2006-11-21 Astrazeneca Ab derivado de quinazolina, composto, composição farmacêutica, uso de derivado de quinazolina, método para produzir um efeito anti-proliferativo em um animal de sangue quente, e, processo para a preparação de um derivado de quinazolina
GB0326459D0 (en) * 2003-11-13 2003-12-17 Astrazeneca Ab Quinazoline derivatives
WO2005075439A1 (en) * 2004-02-03 2005-08-18 Astrazeneca Ab Quinazoline derivatives
US20070232607A1 (en) * 2004-06-04 2007-10-04 Bradbury Robert H Quinazoline Derivatives as Erbb Receptor Tyrosine kinases

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