IP Library Granted Patent US 10,793,559
Granted Patent B2
US 10,793,559 · App. 16/572,917 · Granted Oct 6, 2020

Chemical compounds

Inventors: Niall Andrew Anderson (Stevenage, GB); Nicholas Paul Barton (Stevenage, GB); Sebastien Andre Campos (Stevenage, GB); Edward Paul Cannons (Stevenage, GB); Anthony William James Cooper (Stevenage, GB); Kenneth David Down (Stevenage, GB); Kevin James Doyle (Saffron Walden, GB); Julie Nicole Hamblin (Stevenage, GB); Graham George Adam Inglis (Stevenage, GB); Armelle Le Gall (Stevenage, GB); Vipulkumar Kantibhai Patel (Stevenage, GB); Simon Peace (Stevenage, GB); Andrew Sharpe (Saffron Walden, GB); Gemma Victoria White (Stevenage, GB)
Assignee: GlaxoSmithKline Intellectual Property Development Limited
C07D413/14A61P11/06A61P15/08A61P25/24A61P25/28A61P37/08C07D213/76
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Quick Facts
Patent No.
US 10,793,559
App. No.
16/572,917
Granted
Oct 6, 2020
Kind
B2
Abstract

The invention is directed to certain novel compounds. Specifically, the invention is directed to compounds of formula (I): and salts thereof. The compounds of the invention are inhibitors of kinase activity, in particular PI3-kinase activity.

Claims (11)

1. A method of treating a disorder mediated by inappropriate PI3-kinase activity comprising administering an amount of a compound of formula (I):

wherein

R 1 is C 1-6 alkoxy or —N(C 1-6 alkyl) 2 ,

R 2 is hydrogen or C 1-6 alkyl optionally substituted by —C(O)OC 1-6 alkyl or —OC(O)C 1-6 alkyl,

R 3 , R 4 , R 5 and R 6 are each independently selected from hydrogen and halogen;

R 7 and R 8 are each independently C 1-6 alkyl, or

R 7 and R 8 , together with the nitrogen atom to which they are attached, are linked to form a 5- or 6-membered heterocyclyl wherein the 5- or 6-membered heterocyclyl optionally contains a further nitrogen atom and is optionally substituted by C 3-6 cycloalkyl, 4- to 6-membered heterocyclyl containing one or two heteroatoms independently selected from oxygen and nitrogen, or C 1-6 alkyl wherein the C 1-6 alkyl is optionally substituted by hydroxy or C 1-6 alkoxy, or

R 7 and R 8 , together with the nitrogen atom to which they are attached, are linked to form a 5- or 6-membered heterocyclyl wherein the 5- or 6-membered heterocyclyl contains an oxygen atom and is optionally substituted by one or two substituents independently selected from C 1-6 alkyl;

or a pharmaceutically acceptable salt thereof, to a patient in need thereof, by inhibiting PI3-kinase activity and wherein said disorder mediated by inappropriate PI3-kinase activity is selected from the group consisting of asthma and COPD.

2. A method according to claim 1 wherein the disorder mediated by inappropriate PI3-kinase activity is asthma.

3. A method according to claim 1 wherein the disorder mediated by inappropriate PI3-kinase activity is COPD.

Assignments (1)
CHANGE OF ADDRESS Recorded Oct 8, 2025
From: GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
To: GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
Reel/Frame 073032/0390 →
Priority Claims (1)
GB 1602527.2 · Feb 12, 2016 · national
Continuity (2)
Division 16073355
Related Publication 20200071311A1 · Mar 5, 2020