Substituted indazole derivatives active as kinase inhibitors
US-9616059-B2 · Apr 11, 2017 · US
US10081622B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10081622-B2 |
| Application number | US-201715438872-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 22, 2017 |
| Priority date | Jul 20, 2007 |
| Publication date | Sep 25, 2018 |
| Grant date | Sep 25, 2018 |
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Substituted indazole derivatives of formula (I) and pharmaceutically acceptable salts thereof, as defined in the specification; the compounds of the invention may be useful in therapy in the treatment of diseases associated with a deregulated protein kinase activity, like cancer.
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What is claimed is: 1. A compound which is 5-(3,5-difluorobenzyl)-2-fluoro-benzonitrile, having the structure 2. A method of preparing 5-(3,5-difluoro-benzyl)-1H-indazol-3-ylamine having the structure comprising allowing 5-(3,5-difluorobenzyl)-2-fluoro-benzonitrile to react with hydrazine. 3. A compound which is N-[5-(3,5-difluorobenzyl)-1H-indazol-3-yl]-4-(4-methyl-piperazin-1-yl)-2-[(tetrahydropyran-4-yl)-(2,2,2-trifluoroacetyl)-amino]-benzamide, having the structure or a salt thereof. 4. A method of preparing N-[5-(3,5-difluorobenzyl)-1H-indazol-3-yl]-4-(4-methyl-piperazin-1-yl)-2-(tetrahydropyran-4-ylamino)-benzamide having the structure comprising allowing a compound which is N-[5-(3,5-difluorobenzyl)-1H-indazol-3-yl]-4-(4-methyl-piperazin-1-yl)-2-[(tetrahydropyran-4-yl)-(2,2,2-trifluoroacetyl)-amino]-benzamide, having the structure or a salt thereof, to react with an aqueous solution of a base. 5. The method according to claim 4 , wherein said base is sodium hydrogencarbonate.
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