IP Library Granted Patent US 9,150,579
Granted Patent B2
US 9,150,579 · App. 13/933,856 · Granted Oct 6, 2015

Selective PI3K delta inhibitors

Inventors: Swaroop Kumar V. S. Vakkalanka (La Chaux-de-Fonds, CH); Meyyappan Muthuppalaniappan (Hyderabad, IN); Dhanapalan Nagarathnam (La Chaux-de-Fonds, CH)
Assignee: RHIZEN PHARMACEUTICALS SA
C07D487/04A61K31/519A61K45/06
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Quick Facts
Patent No.
US 9,150,579
App. No.
13/933,856
Granted
Oct 6, 2015
Kind
B2
Abstract

The present invention relates to selective inhibitors of PI3K delta protein kinases, methods of preparing them, pharmaceutical compositions containing them and methods of treatment and/or prevention of kinase mediated diseases or disorders with them.

Claims (19)

1. A compound selected from (S)-2-(1-(4-amino-3-(3-fluoro-4-isopropoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-6-fluoro-3-(3-fluorophenyl)-4H-chromen-4-one and pharmaceutically acceptable salts thereof.

2. A pharmaceutical composition comprising (S)-2-(1-(4-amino-3-(3-fluoro-4-isopropoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-6-fluoro-3-(3-fluorophenyl)-4H-chromen-4-one or a pharmaceutically acceptable salt thereof, wherein the pharmaceutical composition is substantially free of (R)-2-(1-(4-amino-3-(3-fluoro-4-isopropoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-6-fluoro-3-(3-fluorophenyl)-4H-chromen-4-one or a pharmaceutical acceptable salt thereof.

3. The compound of claim 1 , wherein the compound is (S)-2-(1-(4-amino-3-(3-fluoro-4-isopropoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-6-fluoro-3-(3-fluorophenyl)-4H-chromen-4-one 4-methylbenzenesulfonate.

4. The compound of claim 1 , wherein the compound is selected from

(S)-2-(1-(4-amino-3-(3-fluoro-4-isopropoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-6-fluoro-3-(3-fluorophenyl)-4H-chromen-4-one sulphate;

(S)-2-(1-(4-amino-3-(3-fluoro-4-isopropoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-6-fluoro-3-(3-fluorophenyl)-4H-chromen-4-one hydrochloride;

(S)-2-(1-(4-amino-3-(3-fluoro-4-isopropoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-6-fluoro-3-(3-fluorophenyl)-4H-chromen-4-one benzenesulfonate;

(S)-2-(1-(4-amino-3-(3-fluoro-4-isopropoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-6-fluoro-3-(3-fluorophenyl)-4H-chromen-4-one maleate; and

(S)-2-(1-(4-amino-3-(3-fluoro-4-isopropoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-6-fluoro-3-(3-fluorophenyl)-4H-chromen-4-one camphor sulfonate.

5. A pharmaceutical composition comprising a compound of claim 3 and at least one pharmaceutically acceptable carrier.

6. A method for the treatment of leukemia comprising administering to a subject in need thereof an effective amount of a compound of claim 1 .

7. The method of claim 6 , further comprising the step of administering simultaneously or sequentially to a subject in need thereof at least one other anti-cancer agent.

8. A pharmaceutical composition comprising a compound of claim 1 and at least one pharmaceutically acceptable carrier.

9. A pharmaceutical composition comprising a compound of claim and at least one pharmaceutically acceptable carrier.

10. The method of claim 6 , wherein the leukemia is selected from acute leukemia, acute lymphocytic leukemia, acute lymphoblastic leukemia, acute myelocytic leukemia, acute myelogenous leukemia, chronic myelogenous leukemia, myelodysplastic syndrome, promyelocytic leukemia, chronic lymphocytic leukemia, acute myeloid leukemia, chronic granulocytic leukemia, hairy-cell leukemia and erythroleukemia.

11. The compound of claim 1 , wherein the compound has an enantiomeric excess of at least 98%.

12. The compound of claim 3 , wherein the compound has an enantiomeric excess of at least 98%.

13. The composition of claim 2 , wherein the (S)-2-(1-(4-amino-3-(3-fluoro-4-isopropoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-6-fluoro-3-(3-fluorophenyl)-4H-chromen-4-one or a pharmaceutically acceptable salt thereof has an enantiomeric excess of at least 98%.

14. A method for the treatment of leukemia comprising administering to a subject in need thereof an effective amount of a compound of claim 3 .

Assignments (3)
CHANGE OF ADDRESS Recorded Oct 6, 2021
From: RHIZEN PHARMACEUTICALS AG
To: RHIZEN PHARMACEUTICALS AG
Reel/Frame 057836/0286 →
CHANGE OF ADDRESS Recorded Mar 22, 2021
From: RHIZEN PHARMACEUTICALS SA
To: RHIZEN PHARMACEUTICALS SA
Reel/Frame 056775/0375 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 10, 2013
From: VAKKALANKA, SWAROOP KUMAR V.S.; MUTHUPPALANIAPPAN, MEYYAPPAN; NAGARATHNAM, DHANAPALAN
To: RHIZEN PHARMACEUTICALS SA
Reel/Frame 031384/0760 →
Priority Claims (2)
IN 2692/CHE/2012 · Jul 4, 2012 · national
IN 2693/CHE/2012 · Jul 4, 2012 · national
Continuity (3)
Provisional Application 61691561 · Aug 21, 2012
Provisional Application 61691586 · Aug 21, 2012
Related Publication 20140011819A1 · Jan 9, 2014