2,6,7 substituted purines as hdm2 inhibitors
US-2015368247-A1 · Dec 24, 2015 · US
US9556176B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9556176-B2 |
| Application number | US-201214357495-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 8, 2012 |
| Priority date | Nov 9, 2011 |
| Publication date | Jan 31, 2017 |
| Grant date | Jan 31, 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 purine derivatives of formula (I), processes for their preparation, pharmaceutical compositions, and their use in treating viral infections.
Opening claim text (preview).
The invention claimed is: 1. A compound of formula (I) or a pharmaceutically acceptable salt, solvate or polymorph thereof, wherein Y is C 1-4 alkylene, R 1 is selected from the group consisting of imidazolyl, pyrimidyl, pyrrolyl, pyrazolyl, furyl, oxazolyl, oxadiazolyl, isoxazolyl, pyrazinyl and thiazolyl, wherein R 1 is optionally substituted by one or more substituents independently selected from the group consisting of hydroxyl, C 1-6 alkyl, C 1-4 alkoxy, trifluoromethyl, C 3-6 cycloalkyl, phenyl, halogen, hydroxyl-C 1-4 alkyl, C 1-4 -alkoxy-C 1-4 -alkyl- and C 1-4 alkyl-diethoxyphosphoryl R 2 is selected from a group consisting of phenyl, naphtyl, anthracenyl and phenanthrenyl, wherein R 2 is optionally substituted by one or more substituents independently selected from the group consisting of hydroxyl, C 1-6 alkyl, C 1-4 alkoxy, trifluoromethyl, CO 2 R 3 , halogen, hydroxyl-C 1-4 alkyl-, NR 6 R 7 , C(O)R 6 , C(O)NR 6 R 7 , C 1-4 alkyl-diethoxyphosphoryl or C 1-4 alkyl-phosphonic acid; R 3 is selected from H and C 1-6 alkyl; R 6 and R 7 are each independently selected from H, C 1-6 alkyl or C 1-4 alkoxy—after C 1-4 alkyl-diethoxyphosphoryl. 2. A pharmaceutical composition comprising a compound of formula (I) or a pharmaceutically acceptable salt, solvate or polymorph thereof according to claim 1 , together with one or more pharmaceutically acceptable excipients, diluents or carriers. 3. A compound selected from the group consisting of: 4. A pharmaceutical composition comprising a compound of formula (I) or a pharmaceutically acceptable salt, solvate or polymorph thereof according to claim 3 , together with one or more pharmaceutically acceptable excipients, diluents or carriers.
Drugs for immunological or allergic disorders · CPC title
Immunomodulators · CPC title
Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title
Antivirals · CPC title
Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.