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
Links
Landscapes
- 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.
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) |
-
1993
- 1993-12-09 MX MX9307778A patent/MX9307778A/en unknown
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