Preparation of substituted quinazolines

Methods and materials for preparing irreversible inhibitors of tyrosine kinases of general Formula 1 are disclosed. Such inhibitors, which include N-[4-(3-chloro-4-floro-phenylamino)-7-(3-morpholin-4-yl-propoxy)-quinazolin-6-yl]-acrylamide, are useful for treating cancer, restenosis, atherosclerosis...

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Hauptverfasser: SIMON SCHNEIDER, THOMAS ELLIOTT JACKS, ROBERT CRAIG HUGHES, PETER LAURENCE TOOGOOD, KLAUS IRENAUS STEINER, ALEXANDER JAMES BRIDGES, HUBERT GANGOLF KLEMENS BARTH, DENNIS JOSEPH MCNAMARA, ROY THOMAS WINTERS, RONALD JOSEPH HEEMSTRA, NICOLE MARCIA HORNE
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creator SIMON SCHNEIDER
THOMAS ELLIOTT JACKS
ROBERT CRAIG HUGHES
PETER LAURENCE TOOGOOD
KLAUS IRENAUS STEINER
ALEXANDER JAMES BRIDGES
HUBERT GANGOLF KLEMENS BARTH
DENNIS JOSEPH MCNAMARA
ROY THOMAS WINTERS
RONALD JOSEPH HEEMSTRA
NICOLE MARCIA HORNE
description Methods and materials for preparing irreversible inhibitors of tyrosine kinases of general Formula 1 are disclosed. Such inhibitors, which include N-[4-(3-chloro-4-floro-phenylamino)-7-(3-morpholin-4-yl-propoxy)-quinazolin-6-yl]-acrylamide, are useful for treating cancer, restenosis, atherosclerosis, endometriosis and psoriasis. The disclosed methods employ protecting schemes to minimize undesirable diacryloylamino-quinazoline side products.
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subjects CHEMISTRY
HETEROCYCLIC COMPOUNDS
METALLURGY
ORGANIC CHEMISTRY
title Preparation of substituted quinazolines
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