US2018325911A1PendingUtilityA1
Novel compounds
Est. expiryApr 30, 2029(~2.8 yrs left)· nominal 20-yr term from priority
Inventors:Julie Nicole HamblinPaul JonesSuzanne Elaine KeelingJoelle LeCharlotte Jane MitchellNigel James Parr
A61P 9/10A61P 7/00A61P 37/06A61P 37/08A61P 7/02A61P 43/00A61P 3/10A61P 37/00A61P 9/00A61P 25/04A61P 25/28A61P 31/10A61P 25/00A61P 35/00A61P 33/02A61P 31/04A61P 35/02A61P 29/02A61P 31/12A61P 29/00A61P 31/00A61P 15/08A61P 19/02A61P 11/00A61P 13/12A61P 1/18A61P 11/06A61P 1/16A61P 17/00A61P 1/00A61P 11/02C07D 413/14A61K 31/5377A61K 45/06A61K 31/535C07B 2200/13A61K 31/496A61K 31/5375A61K 31/497Y02A50/409Y02A50/30
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Claims
Abstract
and salts thereof. The compounds of the invention are inhibitors of kinase activity, in particular PI3-kinase activity.
Claims
exact text as granted — not AI-modified1 - 12 . (canceled)
13 . A compound of formula (I):
wherein
R 1 is 9- or 10-membered bicyclic heteroaryl wherein the 9- or 10-membered bicyclic heteroaryl contains from one to three heteroatoms independently selected from oxygen and nitrogen and is optionally substituted by C 1-6 alkyl, C 3-6 cycloalkyl, halo, —CN or —NHSO 2 R 5 , or
pyridinyl optionally substituted by one or two substituents independently selected from C 1-6 alkyl, —OR 6 , halo and —NHSO 2 R 7 ;
R 2 and R 3 , together with the nitrogen atom to which they are attached, are linked to form a 6- or 7-membered heterocyclyl wherein the 6- or 7-membered heterocyclyl optionally contains an oxygen atom or a further nitrogen atom;
R 4 is hydrogen or methyl;
R 6 is hydrogen or C 1-4 alkyl; and
R 5 and R 7 are each independently C 1-6 alkyl, or phenyl optionally substituted by one or two substituents independently selected from halo;
or a salt thereof.
14 . The compound according to claim 13 , wherein R 1 is
9-membered bicyclic heteroaryl wherein the 9-membered bicyclic heteroaryl contains one or two nitrogen atoms, or pyridinyl optionally substituted by one or two substituents independently selected from —OR 6 and —NHSO 2 R 7 .
15 . A compound according to claim 13 , wherein R 1 is indolyl.
16 . A compound according to claim 13 , wherein R 1 is pyridinyl optionally substituted by one or two substituents independently selected from —OR 6 and —NHSO 2 R 7 .
17 . A compound according to claim 13 , wherein R 2 and R 3 ,
together with the nitrogen atom to which they are attached, are linked to form a 6-membered heterocyclyl wherein the 6-membered heterocyclyl optionally contains an oxygen atom or a further nitrogen atom.
18 . A compound according to claim 13 , wherein R 2 and R 3 , together with the nitrogen atom to which they are attached, are linked to form a 6-membered heterocyclyl wherein the 6-membered heterocyclyl contains an oxygen atom.
19 . A compound according to claim 13 , wherein R 2 and R 3 , together with the nitrogen atom to which they are attached, are linked to form a 6-membered heterocyclyl wherein the 6-membered heterocyclyl contains a further nitrogen atom.
20 . A compound according to claim 13 , wherein R 4 is hydrogen.
21 . A compound according to claim 13 wherein the compound of formula (I) is in the form of a pharmaceutically acceptable salt thereof.Join the waitlist — get patent alerts
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