IP Library Patent Application 17699582
Patent Application
App. No. 17/699,582

FORMULATIONS OF (S)-3-(1-(9H-PURIN-6-YLAMINO)ETHYL)-8-CHLORO-2-PHENYLISOQUINOLIN-1(2H)-ONE

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Patent No.
US None
App. No.
17/699,582
Abstract

Polymorphs of chemical compounds that modulate kinase activity, including PI3 kinase activity, and compounds, pharmaceutical compositions, and methods of treatment of diseases and conditions associated with kinase activity, including PI3 kinase activity, are described herein. Also provided herein are processes for preparing compounds, polymorphs thereof, and pharmaceutical compositions thereof.

Claims (28)

1 . A compound of Formula (I):

Formula (I), wherein the compound is polymorph Form B, Form C, Form D, Form E, Form F, Form G, Form H, Form I, Form J, or an amorphous form of a compound of Formula (I), or a salt, solvate, or hydrate thereof; or a mixture of two or more thereof.

2 . A mixture of two or more compounds of Formula (I):

wherein the compounds of Formula (I) are selected from:

i) polymorph Form C, or a salt, solvate, or hydrate thereof; and

ii) at least one non-Form C polymorph selected from Form A, Form B, Form D, Form E, Form F, Form G, Form H, Form I, Form J, or an amorphous form of a compound of Formula (I), or a salt, solvate, or hydrate thereof.

3 . A mixture of two or more compounds of Formula (I):

wherein the compounds of Formula (I) are selected from:

i) polymorph Form A, or a salt, solvate, or hydrate thereof; and

ii) at least one non-Form A polymorph selected from Form B, Form C, Form D, Form E, Form F, Form G, Form H, Form I, Form J, or an amorphous form of a compound of Formula (I), or a salt, solvate, or hydrate thereof.

4 . A mixture according to claim 2 , wherein the mixture is at least 50% by weight polymorph Form C, or a salt, solvate, or hydrate thereof.

5 . The compound of claim 1 , which is Polymorph Form C of a compound of Formula (I):

6 . The polymorph according to claim 5 , wherein the polymorph has the following characteristic X-ray Powder Diffraction (XRPD) peaks: 20=10.4° (±0.2°), 13.3° (±0.2°), and 24.3° (±0.2°).

7 . The polymorph according to claim 6 , further comprising at least one characteristic XRPD peak selected from 20=6.6° (±0.2°) and 12.5° (±0.2°).

8 . The polymorph according to claim 5 , wherein the polymorph has the following characteristic XRPD peaks: 20=6.6° (±0.2°), 10.4° (±0.2°), 12.5° (±0.2°), 13.3° (±0.2°), and 24.3° (±0.2°), in combination with at least one XRPD peak selected from 20=8.8° (±0.2°), 9.9° (±0.2°), 13.4° (±0.2°), 15.50 (±0.2°), 16.9° (±0.2°), 19.8° (±0.2°), 21.3° (±0.2°), 23.6° (±0.2°), 25.3° (±0.2°), and 27.9° (±0.2°).

9 . The polymorph according to claim 5 , wherein the polymorph has substantially all peaks in its XRPD pattern as shown in FIG. 3 .

10 . The compound of claim 1 , which is Polymorph Form B of a compound of Formula (I):

11 . The polymorph according to claim 10 , wherein the polymorph has the following characteristic XRPD peaks: 20=7.9° (±0.2°), 13.4° (±0.2°), and 23.4° (±0.2°).

12 . The polymorph according to claim 11 , further comprising at least one characteristic XRPD peak selected from 20=14.0° (±0.2°) and 15.0° (±0.2°).

13 . The polymorph according to claim 10 , wherein the polymorph has the following characteristic XRPD peaks: 20=7.9° (±0.2°), 13.4° (±0.2°), 14.0° (±0.2°), 15.0° (±0.2°), and 23.4° (±0.2°), in combination with at least one XRPD peak selected from 20=9.5° (±0.2°), 12.7° (±0.2°), 13.6° (±0.2°), 14.2° (±0.2°), 15.7° (±0.2°), 19.0° (±0.2°), 22.3° (±0.2°), 24.2° (±0.2°), 24.8° (±0.2°), and 26.9° (±0.2°).

14 . The polymorph according to claim 10 , wherein the polymorph has substantially all peaks in its XRPD pattern as shown in FIG. 2 .

15 . The compound of claim 1 , which is Polymorph Form D of a compound of Formula (I):

16 . The polymorph according to claim 15 , wherein the polymorph has the following characteristic XRPD peaks: 20=11.4° (±0.2°), 17.4° (±0.2°), and 22.9° (±0.2°).

17 . The polymorph according to claim 16 , further comprising at least one characteristic XRPD peak selected from 20=9.2° (±0.2°) and 18.3° (±0.2°).

18 . The polymorph according to claim 15 , wherein the polymorph has the following characteristic XRPD peaks: 20=9.2° (±0.2°), 11.4° (±0.2°), 17.4° (±0.2°), 18.3° (±0.2°), and 22.9° (±0.2°), in combination with at least one XRPD peak selected from 20=9.8° (±0.20), 12.2° (±0.2°), 15.8° (±0.2°), 16.2° (±0.2°), 16.8° (±0.2°), 18.9° (±0.2°), 19.9° (±0.2°), 20.0° (±0.2°), 24.9° (±0.2°), and 29.3° (±0.2°).

19 . The polymorph according to claim 15 , wherein the polymorph has substantially all peaks in its XRPD pattern as shown in FIG. 4 .

20 . The compound of claim 1 , which is Polymorph Form E of a compound of Formula (I):

21 - 68 . (canceled)

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 20, 2022
From: ISBESTER, PAUL
To: ALBANY MOLECULAR RESEARCH, INC.
Reel/Frame 059654/0258 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 20, 2022
From: ALBANY MOLECULAR RESEARCH, INC.
To: INTELLIKINE, INC.
Reel/Frame 059654/0304 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 20, 2022
From: REN, PINGDA; MARTIN, MICHAEL
To: INTELLIKINE LLC
Reel/Frame 059654/0310 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 20, 2022
From: INTELLIKINE LLC
To: INFINITY PHARMACEUTICALS, INC.
Reel/Frame 059654/0347 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 20, 2022
From: LANE, BENJAMIN S.; KROPP, JASON
To: INFINITY PHARMACEUTICALS, INC.
Reel/Frame 059654/0354 →
CHANGE OF NAME Recorded Apr 20, 2022
From: INTELLIKINE, INC.
To: INTELLIKINE LLC
Reel/Frame 059715/0588 →