Pyridazinedione-based heterobicyclic covalent linkers and methods and applications thereof
US-2024425465-A1 · Dec 26, 2024 · US
US9765076B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9765076-B2 |
| Application number | US-201414514687-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 15, 2014 |
| Priority date | Nov 16, 2006 |
| Publication date | Sep 19, 2017 |
| Grant date | Sep 19, 2017 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present invention relates to compounds and methods for the treatment of cancer. In particular, the invention provides potent inhibitors of Aurora A kinase, pharmaceutical compositions comprising the compounds, and methods of using the compounds for the treatment of cancer.
Opening claim text (preview).
What is claimed is: 1. A process for preparing the compound (1): said process comprising reacting a compound of formula (iv): with a compound of formula (v): 2. The process of claim 1 , further comprising converting the compound (1) into a sodium salt thereof. 3. The process of claim 2 , wherein said converting comprises reacting the compound (1) with sodium hydroxide. 4. The process of claim 1 , wherein said reacting is carried out in the presence of methanol and potassium carbonate. 5. The process of claim 4 , further comprising converting the compound (1) into a sodium salt thereof. 6. The process of claim 5 , wherein said converting comprises reacting the compound (1) with sodium hydroxide. 7. A process for preparing sodium 4-{[9-chloro-7-(2-fluoro-6-methoxy phenyl)-5H-pyrimido[5,4-d][2]benzazepin-2-yl]amino}-2-methoxybenzoate, comprising reacting 4-{[9-chloro-7-(2-fluoro-6-methoxyphenyl)-5H-pyrimido[5,4-d][2]benzazepin-2-yl]amino}-2-methoxybenzoic acid with sodium hydroxide.
Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title
Antineoplastic agents · CPC title
Ortho-condensed systems · CPC title
having seven-membered rings, e.g. azelastine, pentylenetetrazole · CPC title
ortho- or peri-condensed with heterocyclic rings · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.