MX9307778A - QUINAZOLINE DERIVATIVES. - Google Patents

QUINAZOLINE DERIVATIVES.

Info

Publication number
MX9307778A
MX9307778A MX9307778A MX9307778A MX9307778A MX 9307778 A MX9307778 A MX 9307778A MX 9307778 A MX9307778 A MX 9307778A MX 9307778 A MX9307778 A MX 9307778A MX 9307778 A MX9307778 A MX 9307778A
Authority
MX
Mexico
Prior art keywords
alkoxy
hydroxy
amino
alkyl
membered bicyclic
Prior art date
Application number
MX9307778A
Other languages
Spanish (es)
Inventor
Andrew John Barker
Dearg Sutherland Brown
Original Assignee
Zeneca 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
Priority claimed from GB929225765A external-priority patent/GB9225765D0/en
Priority claimed from GB939310248A external-priority patent/GB9310248D0/en
Priority claimed from GB939323290A external-priority patent/GB9323290D0/en
Application filed by Zeneca Ltd filed Critical Zeneca Ltd
Publication of MX9307778A publication Critical patent/MX9307778A/en

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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

La presente invención se refiere a derivados de quinazolina de la fórmula I: en donde m es 1,2 o 3, y y cada una de R1 incluye, hidróxi, amino, ureido, hidroxiamino, triflurometoxi, alquilo de 1-4C. alcoxi de 1-4C, y alquilenodioxi de 1-3C, y Q es una fracción del heterociclo biciclico de 9- o 10-miembros que contiene uno o dos hetero átomos de nitrógeno, y que contiene opcionalmente un heteroátomo adicional seleccionado de nitrógeno, oxígeno o azufre, o Q es una fracción de arilo biciclico de 9- o 10-miembros, con la fracción del heterociclo o del arilo, que puede tener opcionalmente uno o dos substituyentes seleccionados de halógeno, hidroxi, oxo, amino, nitro, carbamoilo, alquilo de 1-4C, alcoxi de 1-4C, o una sal farmaceúticamente aceptable del mismo. Un procedimiento para su preparación, a las composiciones farmacéuticas que contienen a los mismos, y al uso de las propiedades inhibitorias de la quinasa de tirosina de receptor, de los compuestos en el tratamiento del cáncer.The present invention relates to quinazoline derivatives of the formula I: where m is 1,2 or 3, and and each of R1 includes, hydroxy, amino, ureido, hydroxyamino, trifluromethoxy, 1-4C-alkyl. 1-4C alkoxy, and 1-3C alkylenedioxy, and Q is a fraction of the 9- or 10-membered bicyclic heterocycle containing one or two nitrogen hetero atoms, and optionally containing an additional hetero atom selected from nitrogen, oxygen or sulfur, or Q is a 9- or 10-membered bicyclic aryl moiety, with the heterocycle or aryl moiety, which may optionally have one or two substituents selected from halogen, hydroxy, oxo, amino, nitro, carbamoyl, 1-4C-alkyl, 1-4C-alkoxy, or a pharmaceutically acceptable salt thereof. A process for their preparation, to the pharmaceutical compositions containing them, and to the use of the inhibitory properties of receptor tyrosine kinase, of the compounds in the treatment of cancer.

MX9307778A 1992-12-10 1993-12-09 QUINAZOLINE DERIVATIVES. MX9307778A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB929225765A GB9225765D0 (en) 1992-12-10 1992-12-10 Quinazoline derivatives
GB939310248A GB9310248D0 (en) 1993-05-18 1993-05-18 Quinazoline derivatives
GB939323290A GB9323290D0 (en) 1992-12-10 1993-11-11 Quinazoline derivatives

Publications (1)

Publication Number Publication Date
MX9307778A true MX9307778A (en) 1994-07-29

Family

ID=27266502

Family Applications (1)

Application Number Title Priority Date Filing Date
MX9307778A MX9307778A (en) 1992-12-10 1993-12-09 QUINAZOLINE DERIVATIVES.

Country Status (1)

Country Link
MX (1) MX9307778A (en)

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