Process for preparing crystalline sorafenib tosylate

Patent metadata

Field	Value
Publication number	US-2015111929-A1
Application number	US-201214381226-A
Country	US
Kind code	A1
Filing date	Dec 31, 2012
Priority date	May 23, 2012
Publication date	Apr 23, 2015
Grant date	—

Abstract

The present invention provides an industrially suitable process for the preparation of substantially pure 4-{4-[({[4-chloro-3-(trifluoromethyl)-phenyl]amino}carbonyl)amino]phenoxy}-N-methylpyridine-2-carboxamide or Sorafenib and its tosylate salt, with a suitable impurity profile and without requirement of any additional purification steps. The present invention also provides Sorafenib base (II) as stable crystalline Form-SSB.
The present invention further relates to a process for the preparation of crystalline Sorafenib tosylate Form-I which is free from contamination of any other polymorphic form of Sorafenib tosylate, for e.g. Form II or Form III, and does not involve any seeding requirement for crystallization step.

First claim

We claim:

1 . A process for the preparation of crystalline Sorafenib base-Form-SSB, comprising reacting 4-(4-aminophenoxy)-N-methylpicolinamide (III) with 4-chloro-3-(trifluoro methyl)phenylisocyanate (IV) in a high boiling organic solvent at a temperature ranging between 75-90° C., to yield crystalline Sorafenib base-Form-SSB.

2 . A process for the preparation of crystalline Sorafenib base-Form-SSB according to claim 1 , wherein the high boiling organic solvent is selected from C 4-8 ketones or a mixture thereof.

3 . A process for the preparation of crystalline Sorafenib base-Form-SSB according to claim 1 , wherein C 4-8 ketone is selected from methyl ethyl ketone (MEK) or methyl isobutyl ketone (MIBK).

4 . A process for the preparation of crystalline Sorafenib base-Form-SSB according to claim 1 , wherein reaction of 4-(4-aminophenoxy)-N-methylpicolinamide (III) with 4-chloro-3-(trifluoromethyl)phenylisocyanate (IV), is carried out at temperature ranging between 75-90° C.

5 . A process for the preparation of crystalline Sorafenib base-Form-SSB according to claim 1 , wherein crystalline Sorafenib base-Form-SSB obtained is characterized by X-ray powder diffraction pattern substantially according to FIG. 1 and DSC isothermal pattern substantially according to FIG. 2 .

6 . Crystalline Sorafenib base-Form-SSB, characterized by X-ray powder diffraction pattern comprising at least 5 characteristic 2θ° peaks selected from the XRPD peak set of 9.9, 11.4, 12.6, 14.6, 15.2, 15.6, 18.1, 18.6, 21.8, 22.5, 22.9, 23.6, 24.8, 25.2±0.20 2θ° and DSC isotherm comprising a single endothermic peak ranging between 202 to 212° C.

7 . Crystalline Sorafenib base-Form-SSB according to claim 6 , characterized by X-ray powder diffraction pattern substantially according to FIG. 1 and DSC isothermal pattern substantially according to FIG. 2 .

8 . A process for the preparation of Sorafenib tosylate using crystalline Sorafenib base-Form-SSB, comprising steps of:
a) reacting 4-(4-aminophenoxy)-N-methylpicolinamide (III) with 4-chloro-3-(trifluoromethyl)phenylisocyanate (IV) in a high boiling organic solvent at a temperature ranging between 75-90° C., to yield crystalline Sorafenib base (II)-Form-SSB; and

b) combining crystalline Sorafenib base (II)-Form-SSB with p-toluenesulfonic acid in the presence of methyl ethyl ketone at a temperature below 35° C., to give Sorafenib tosylate (I).

9 . A process for the preparation of Sorafenib tosylate using crystalline Sorafenib base-Form-SSB according to claim 8 , wherein the high boiling organic solvent is selected from C 4-8 ketones or a mixture thereof.

10 . A process for the preparation of Sorafenib tosylate using crystalline Sorafenib base-Form-SSB according to claim 8 , wherein C 4-8 ketone is selected from methyl ethyl ketone (MEK) or methyl isobutyl ketone (MIBK).

11 . A process for the preparation of Sorafenib tosylate using crystalline Sorafenib base-Form-SSB according to claim 8 , wherein reaction of 4-(4-aminophenoxy)-N-methylpicolinamide (III) with 4-chloro-3-(trifluoromethyl)phenylisocyanate (IV), is carried out at temperature ranging between 75-90° C.

12 . A process for the preparation of Sorafenib tosylate using crystalline Sorafenib base-Form-SSB according to claim 8 , wherein the obtained final product is crystalline Sorafenib tosylate Form-I characterized by X-ray powder diffraction pattern substantially according to FIG. 4 .

13 . A pharmaceutical composition comprising crystalline Sorafenib base-Form-SSB according to claim 6 , together with one or more pharmaceutically acceptable excipients.

Assignees

• Shilpa Medicare Ltd

Inventors

• Purohit Prashant
• Rampalli Sriram
• Vijaya Murali Mohanrao Seshagiri
• Upalla Lavkumar

Classifications

• A61P35/00

  Antineoplastic agents · CPC title

• A61K31/44

  Non condensed pyridines; Hydrogenated derivatives thereof · CPC title

• C07D213/81 Primary

  Amides; Imides · CPC title