[4-(6-FLUORO-7-METHYLAMINO-2,4-DIOXO-1,4-DIHYDRO-2H-QUINAZOLIN-3-YL)-PHENYL]-5-CHLORO-THIOPHEN-2-YL-SULFONYLUREA SALTS, FORMS AND METHODS RELATED THERETO
The present invention provides novel sulfonylurea salts of a salt of formula (I) and polymorph forms thereof. The compounds in their various forms are effective platelet ADP receptor inhibitors and may be used in various pharmaceutical compositions, and are particularly effective for the prevention and/or treatment of cardiovascular diseases, particularly those diseases related to thrombosis. The invention also provides a method for preparing such compounds and forms and for preventing or treating thrombosis and thrombosis related conditions in a mammal comprising the step of administering a therapeutically effective amount of a salt of formula (I) or a pharmaceutically acceptable form thereof.
1 . A salt comprising a compound Formula I:
and an ion selected from the group consisting of sodium, potassium, calcium, L-lysine, ammonium, magnesium, L-arginine, tromethamine, N-ethylglucamine and N-methylglucamine.
2 .- 9 . (canceled)
10 . A salt having the formula:
in a crystalline solid form C characterized by at least one of:
(i) an X-ray powder diffraction pattern substantially in accordance with FIG. 15 ; and
(ii) a DSC scan substantially in accordance with the DSC pattern shown in FIG. 20 .
11 .- 12 . (canceled)
13 . A salt having the formula:
in a crystalline solid form D characterized by at least one of:
(i) an X-ray powder diffraction pattern substantially in accordance with FIG. 21 ; and
(ii) a DSC scan substantially in accordance with the DSC pattern shown in FIG. 24 .
14 .- 15 . (canceled)
16 . A salt having the formula:
in a crystalline solid form A which provides at least one of:
(i) an X-ray powder diffraction pattern substantially in accordance with FIG. 25 ; and
(ii) a DSC scan substantially in accordance with FIG. 29 .
17 .- 18 . (canceled)
19 . A salt having the formula:
in a crystalline solid form B which provides at least one of:
(i) an X-ray powder diffraction pattern substantially in accordance with FIG. 30 ; and
(ii) a TGA scan substantially in accordance with FIG. 31 .
20 . (canceled)
21 . A salt having the formula:
in a crystalline solid form C which provides at least one of:
(i) an X-ray powder diffraction pattern substantially in accordance with FIG. 32 ; and
(ii) a DSC scan substantially in accordance with FIG. 34 .
22 .- 23 . (canceled)
24 . A salt having the formula:
in a crystalline solid form A which provides at least one of:
(i) an X-ray powder diffraction pattern substantially in accordance with FIG. 37 ; and
(ii) a DSC scan substantially in accordance with FIG. 43 .
25 .- 26 . (canceled)
27 . A salt having the formula:
in a crystalline solid form A which provides at least one of:
(i) an X-ray powder diffraction pattern substantially in accordance with FIG. 44 ; and
(ii) a DSC scan substantially in accordance with FIG. 48 .
28 .- 30 . (canceled)
31 . A pharmaceutical composition comprising a therapeutically effective amount of a compound according to claim 1 and a pharmaceutically acceptable vehicle or carrier.
32 .- 42 . (canceled)
43 . A pharmaceutical composition comprising a therapeutically effective amount of a compound according to claim 1 and an additional therapeutic agent.
44 . (canceled)
45 . A pharmaceutical composition for preventing or treating a condition in a mammal characterized by undesired thrombosis comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a salt of claim 1 .
46 . A method of preparing a salt of formula I:
comprising contacting a base with a compound of formula II:
or a salt thereof under conditions to form the salt of formula I.
47 .- 51 . (canceled)
52 . A method for preventing or treating thrombosis and thrombosis related conditions in a mammal comprising the step of administering to a mammal a therapeutically effective amount of a salt of claim 1 .
53 . A method for preventing or treating a condition or disorder mediated at least in part by ADP-induced platelet aggregation in a mammal comprising the step of administering to a mammal in need of such treatment in a therapeutically effective amount of a composition of claim 1 or a pharmaceutically acceptable salt thereof.
54 . A method for inhibiting the coagulation of a blood sample comprising the step of contacting said sample with said salt a salt of claim 1 .
55 .- 64 . (canceled)
65 . A method for preventing the occurrence of a secondary ischemic event comprising administering to a patient who has suffered a primary ischemic event a therapeutically effective amount of a salt of claim 1 , together with a pharmaceutically acceptable carrier.
66 .- 67 . (canceled)
68 . A method for the preparation of a pharmaceutical composition comprising admixing a therapeutically effective amount of the salt of claim 1 with a pharmaceutically acceptable vehicle or carrier.