Solid forms of ingenol 3-(3,5-diethylisoxazole-4-carboxylate) and method for preparing the same

Patent metadata

Field	Value
Publication number	US-2019210980-A1
Application number	US-201716330909-A
Country	US
Kind code	A1
Filing date	Aug 29, 2017
Priority date	Sep 6, 2016
Publication date	Jul 11, 2019
Grant date	—

Abstract

Disclosed are solid forms of ingenol 3-(3,5-diethylisoxazole-4-carboxylate) selected from an amorphous form or a crystalline anhydrous form. Also disclosed are solid solvates of ingenol 3-(3,5-diethylisoxazole-4-carboxylate) selected from an acetone solvate, a dimethylcarbonate solvate, an isopropyl ether solvate, an acetonitrile solvate, a toluene solvate, a mesitylene solvate, a nitromethane solvate, a dichloromethane/heptane solvate and an ethyl acetate solvate, for use as intermediates.

First claim

1 . Solid forms of ingenol 3-(3,5-diethylisoxazole-4-carboxylate) selected from an amorphous form or a crystalline anhydrous form.

2 . The amorphous solid form of claim 1 characterized by a XRPD pattern showing absence of diffraction peaks, a FTIR spectrum having peaks at about 2940-1708-1597-1444-1380-1288-1188-1105-1033-959-880-803-678±4 cm −1 and by a Glass Transition (Tg) approximately between 60° C. and 110° C. with a maximum at about 76° C.

3 . The crystalline anhydrous form of claim 1 characterized by a XRPD pattern showing peaks at about 6.0-9.4-11.9-13.2-13.8-15.3-19.1-20.1-24.0-28.1±0.2 degrees two theta, a FTIR pattern with peaks at about 3582-3416-2979-2940-1709-1594-1442-1380-1288-1103-1030-959-881-794-686±4 cm −1 and by a TG/DTA thermogram showing an endothermic signal with maximum at about 100.5° C. and a melting peak with maximum at about 134.4° C.

4 . Solid solvates of ingenol 3-(3,5-diethylisoxazole-4-carboxylate) selected from an acetone solvate, a dimethylcarbonate solvate, an isopropyl ether solvate, an acetonitrile solvate, a toluene solvate, a mesitylene solvate, a nitromethane solvate, a dichloromethane/heptane solvate and an ethyl acetate solvate, for use as intermediates.

5 . The acetone solvate of claim 4 characterized by a XRPD pattern showing peaks at about 5.7-8.5-11.4-12.1-13.1-15.4-19.1-20.6-21.6-24.0±0.2 degrees two theta, by a FTIR pattern with peaks at about 3579-3478-3364-2940-1711-1695-1595-1442-1358-1217-1105-1033-959-880-793-684±4 cm −1 and by a TG/DTA thermogram showing an endothermic signal with maximum at about 123.1° C. associated with a weight loss of about 5% and a melting peak with maximum at about 134.3° C.

6 . The dimethylcarbonate solvate of claim 4 characterized by a XRPD pattern showing peaks at about 5.7-8.4-10.1-11.6-13.0-14.0-15.4-19.3-21.7-23.4±0.2 degrees two theta, by a FTIR pattern with peaks at about 3581-3473-2939-1754-1709-1696-1594-1441-1287-1151-1105-1030-959-880-794-685±4 cm −1 and by a TG/DTA thermogram showing an endothermic signal with maximum at about 137.0° C. associated with a weight loss of about 6-7%.

7 . The isopropyl ether solvate of claim 4 characterized by a XRPD pattern showing peaks at about 5.9-9.2-10.4-11.8-11.9-13.1-13.6-15.1-17.9-22.2-24.1-30.3±0.2 degrees two theta, by a FTIR pattern with peaks at about 3581-3463-2940-1705-1644-1595-1456-1442-1288-1152-1105-1029-959-881-837-794-686±4 cm −1 and by a TG/DTA thermogram showing a weak endothermic signal below 100° C. and an endothermic peak with a maximum at about 135.7° C. associated with a weight loss of about 11.0% at 133° C.

8 . The acetonitrile solvate of claim 4 characterized by FTIR spectrum with peaks at 3581-3474-3378-2940-1706-1644-1596-1456-1312-1288-1152-1104-1076-1049-1030-959-880-794-685±4 cm −1 and by a TG/DTA thermogram showing a weak endothermic signal with maximum at about 124.4° C. associated with a weight loss of about 1.3% at 126° C.

9 . The toluene solvate of claim 4 characterized by a XRPD pattern showing peaks at about 5.6-5.7-8.4-8.5-10.3-11.4-11.5-12.1-13.1-14.1-15.4-19.3-21.6-23.2±0.2 degrees two theta, by a FTIR pattern with peaks at about 3576-3481-2874-1706-1693-1640-1597-1497-1455-1309-1295-1106-1074-1049-1003-958-880-837-794-730-696-684-649±4 cm −1 and by a weak endothermic signal at a maximum at about 123.4 associated with a weight loss of about 8.4% at 129° C.

10 . The nitromethane solvate of claim 4 characterized by a XRPD pattern showing peaks at about 5.8-8.6-9.0-10.4-11.7-13.2-14.1-15.6-21.9-23.6-24.2±0.2 degrees two theta, by a FTIR pattern with peaks at about 3579-3476-2876-1710-1643-1596-1560-1442-1358-1336-1288-1218-1105-1030-959-880-837-794-685±4 cm −1 and by a TG/DTA thermogram showing a double endothermic peak with maxima at about 125.4 and 133.9 associated with a weight loss of about 5.8% at 140° C.

11 . Mesitylene solvate of claim 4 characterized by a XRPD pattern showing peaks at about 5.3-6.0-9.1-10.5-12.1-13.0-14.8-18.2-22.3-24.3-25.8-28.6-30.6-34.7±0.2 degrees two theta, a FTIR spectrum with peaks at about 3580-3479-2876-1705-1642-1595-1560-1455-1441-1381-1311-1288-1150-1105-1074-1029-1003-958-880-836-794-685±4 cm −1 and by a TG/DTA thermogram showing an endothermic peak with maximum at about 133.2° C. associated with a weight loss of about 2.0% at 131° C.

12 . The dichloromethane/heptane solvate of claim 4 characterized by a XRPD pattern showing peaks at about 5.7-8.6-9.0-10.4-11.6-12.2-12.9-14.4-15.5-17.5-19.9-21.7-22.4-28.1-29.4±0.2 degrees two theta, by a FTIR spectrum with peaks at about 3578-3474-2876-1705-1652-1596-1454-1442-1288-1217-1152-1105-1075-1050-1030-1003-958-880-837-794-770-739-700-685±4 cm −1 and by an endothermic signal with maximum at about 130.7° C. associated with a weight loss of about 4.1% between 130 and 135° C.

13 . The ethyl acetate solvate of claim 4 characterized by a XRPD pattern showing peaks at about 5.8-8.6-10.0-11.6-12.7-13.1-14.0-15.6-16.0-19.1-20.2-22.0-23.2±0.2 degrees two theta and by a TG/DTA thermogram showing an endothermic signal with maximum at about 123.8° C. associated with a weight loss of about 5.4% at about 130° C.

Assignees

• Indena Spa

Inventors

• Allegrini Pietro
• Peterlongo Federico
• Gambini Andrea
• Ciceri Daniele
• Sardone Nicola
• Ricotti Maurizio

Classifications

• C07B2200/13

  Crystalline forms, e.g. polymorphs · CPC title

• C07D261/18 Primary

  Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen · CPC title