IP Library Granted Patent US 9,453,039
Granted Patent B2
US 9,453,039 · App. 13/938,763 · Granted Sep 27, 2016

Crystal structures of SGLT2 inhibitors and processes for preparing same

Inventors: Jack Z. Gougoutas (Princeton, NJ); Hildegard Lobinger (Princeton, NJ); Srividya Ramakrishnan (Princeton, NJ); Prashant P. Deshpande (Princeton, NJ); Jeffrey T. Bien (Princeton, NJ); Chiajen Lai (Princeton, NJ); Chenchi Wang (Princeton, NJ); Peter Riebel (Princeton, NJ); John Anthony Grosso (Princeton, NJ); Alexandra A. Nirschl (Princeton, NJ); Janak Singh (Princeton, NJ); John D. DiMarco (Princeton, NJ)
Assignee: AstraZeneca AB
C07H15/207A61K31/7034A61K45/06C07H7/04
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Quick Facts
Patent No.
US 9,453,039
App. No.
13/938,763
Granted
Sep 27, 2016
Kind
B2
Abstract

The present invention relates to physical crystal structures of a compound of the formula I: wherein R 1 , R 2 , R 2a , R 3 and R 4 are as defined herein, especially pharmaceutical compositions containing structures of compound I or II, processes for preparing same, intermediates used in preparing same, and methods of treating diseases such as diabetes using such structures.

Claims (12)

1. A crystalline structure of a compound of formula I

which is (R)-PG (form SD-3).

2. The crystalline structure according to claim 1 , in substantially pure form.

3. The crystalline structure (R)-PG (form SD-3) according to claim 1 having the formula 1b

4. The crystalline structure according to claim 3 characterized by one or more of the following:

a) a powder x-ray diffraction pattern comprising 2θ values (CuKα λ=1.5418 Å) of 3.9±0.1, 8.0±0.1, 8.7±0.1, 15.3±0.1, 15.6±0.1, 17.2±0.1, 19.2±0.1, 19.9±0.1 and 20.3±0.1, at room temperature;

b) a solid state 13 C NMR spectrum having substantially similar peak positions at 15.8, 17.6, 39.0, 60.9, 63.2, 67.4, 69.7, 77.3, 79.2, 79.8, 113.3, 123.6, 129.0, 130.4, 132.0, 135.6, 139.2 and 157.9 ppm, as determined on a 400 MHz spectrometer relative to TMS at zero;

c) a differential scanning calorimetry thermogram having an endotherm in the range of about 43° C. to 60° C. or as shown in FIG. 8 ; or

d) thermal gravimetric analysis curve with about 18.7% weight loss from about room temperature up to about 235° C. or as shown in FIG. 6 .

5. A pharmaceutical composition comprising an effective amount of a crystal structure of a compound of formula I according to claim 1 and a pharmaceutically acceptable carrier or diluent.

6. The pharmaceutical composition according to claim 5 wherein the crystalline structure is in substantially pure form.

7. A pharmaceutical composition comprising an effective amount of the crystal structure according to claim 1 in combination with one or more therapeutic agents selected from the group consisting of an antidiabetic agent, a anti-hypertensive agent, an anti-atherosclerotic agent and a lipid-lowering agent.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE ADDRESS PREVIOUSLY RECORDED ON REEL 032541 FRAME 0698. ASSIGNOR(S) HEREBY CONFIRMS THE ADDRESS OF THE ASSIGNEE SHOULD BE SE-151 85, SODERTALJE, SWEDEN. Recorded May 9, 2014
From: BRISTOL-MYERS SQUIBB COMPANY
To: ASTRAZENECA AB
Reel/Frame 032858/0978 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 27, 2014
From: BRISTOL-MYERS SQUIBB COMPANY
To: ASTRAZENECA AB
Reel/Frame 032541/0698 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 11, 2013
From: GOUGOUTAS, JACK Z.; RAMAKRISHNAN, SRIVIDYA; DESHPANDE, PRASHANT P.; BIEN, JEFFREY T.; GROSSO, JOHN ANTHONY; NIRSCHL, ALEXANDRA A.; SINGH, JANAK; LAI, CHIAJEN; WANG, CHENCHI; DIMARCO, JOHN D.; LOBINGER, HILDEGARD; RIEBEL, PETER
To: BRISTOL-MYERS SQUIBB COMPANY
Reel/Frame 030778/0937 →
Continuity (4)
Division 13049712 · Mar 16, 2011
Division 11765481 · Jun 20, 2007
Provisional Application 60817118 · Jun 28, 2006
Related Publication 20130303467A1 · Nov 14, 2013