US2018222893A1PendingUtilityA1
Heteroaromatic compounds as btk inhibitors
Est. expiryDec 16, 2035(~9.4 yrs left)· nominal 20-yr term from priority
Inventors:Todd BosanacJoerg BentzienMichael J. BurkeRyan Michael FryerEric T. LarsonWang MaoBryan MckibbenYue ShenFariba SoleymanzadehMatt Aaron Tschantz
A61P 37/00A61P 9/00A61P 37/08A61P 35/02A61P 37/06A61P 7/00A61P 37/02A61P 29/00A61P 27/02A61P 17/00A61P 17/04A61P 11/06A61P 25/00A61P 13/12A61P 11/02A61P 1/04A61P 19/02C07D 401/14A61K 31/4155C07D 403/14
62
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
wherein the groups R1, Cy and Y are defined herein, which are suitable for the treatment of diseases related to BTK, and processes for making these compounds, pharmaceutical preparations containing these compounds, and their methods of use.
Claims
exact text as granted — not AI-modified1 - 23 . (canceled)
24 . A compound of the formula (I)
wherein:
Cy is chosen from
each R 1 is independently chosen from hydrogen or methyl;
R 2 is L-Ar, wherein Ar is phenyl or pyridinyl and each is optionally substituted by one or more of halogen, halo C 1-4 alkyl, C 1-4 alkyl, C 1-4 alkoxy, —CN, halo C 1-4 alkoxy, or cycloalkyl;
L is —(CH 2 )— or —(CHCH 3 )—;
Y is C 6 -C 8 spirocycle containing 1 ring nitrogen atom, and is substituted by one R 3 ;
R 3 is chosen from
and
each R 4 is independently chosen from hydrogen, C 1-4 alkyl, or C 3-4 cycloalkyl;
each group defined above for R 1 -R 4 and Y can be where possible partially or fully halogenated;
or a pharmaceutically acceptable salt thereof.
25 . The compound according to claim 24 , wherein
Y is chosen from
or a pharmaceutically acceptable salt thereof.
26 . The compound according to claim 24 , wherein
Cy is
or a pharmaceutically acceptable salt thereof.
27 . The compound according to claim 24 and wherein
Cy is
or a pharmaceutically acceptable salt thereof.
28 . The compound according to claim 24 chosen from:
or a pharmaceutically acceptable salt thereof.
29 . The compound according to claim 28 of the formula:
or a pharmaceutically acceptable salt thereof.
30 . The compound according to claim 28 of the formula:
or a pharmaceutically acceptable salt thereof.
31 . The compound according to claim 28 of the formula:
or a pharmaceutically acceptable salt thereof.
32 . The compound according to claim 28 of the formula:
or a pharmaceutically acceptable salt thereof.
33 . The compound according to claim 28 of the formula:
or a pharmaceutically acceptable salt thereof.
34 . The compound according to claim 28 of the formula:
or a pharmaceutically acceptable salt thereof.
35 . The compound according to claim 28 of the formula:
or a pharmaceutically acceptable salt thereof.
36 . The compound according to claim 28 of the formula:
or a pharmaceutically acceptable salt thereof.
37 . The compound according to claim 28 of the formula:
or a pharmaceutically acceptable salt thereof.
38 . The compound according to claim 28 of the formula:
or a pharmaceutically acceptable salt thereof.
39 . The compound according to claim 28 of the formula:
or a pharmaceutically acceptable salt thereof.
40 . The compound according to claim 28 of the formula:
or a pharmaceutically acceptable salt thereof.
41 . The compound according to claim 28 of the formula:
or a pharmaceutically acceptable salt thereof.
42 . A pharmaceutical composition comprising a therapeutically effective amount of a compound according to claim 24 or a pharmaceutically acceptable salt thereof.
43 . A method of treating a disease chosen from rheumatoid arthritis, systemic lupus erythromatosis, lupus nephritis, Sjogren's disease, vasculitis, scleroderma, asthma, allergic rhinitis, allergic eczema, B cell lymphoma, multiple sclerosis, juvenile rheumatoid arthritis, juvenile idiopathic arthritis, inflammatory bowel disease, graft versus host disease, psoriatic arthritis, ankylosing spondylitis and uveitis, comprising administering to a patient a therapeutically effective amount of a compound according to claim 24 or a pharmaceutically acceptable salt thereof.Cited by (0)
No later patents cite this yet.
References (0)
No backward citations on record.