Solid state forms of Lenvatinib Mesylate

Patent metadata

Field	Value
Publication number	US-11084791-B2
Application number	US-201716473101-A
Country	US
Kind code	B2
Filing date	Dec 29, 2017
Priority date	Dec 29, 2016
Publication date	Aug 10, 2021
Grant date	Aug 10, 2021

Abstract

The present invention provides a crystalline form of Lenvatinib Mesylate, processes for the preparation of crystalline form of lenvatinib Mesylate and pharmaceutical compositions thereof. The crystalline form of lenvatinib Mesylate designated as Form VN1 is characterized by powder X-ray diffraction pattern. The present invention further provides a process for the preparation of amorphous form of lenvatinib Mesylate. The amorphous form is characterized by powder X-ray diffraction pattern.

First claim

The invention claimed is:

1. Methyl Isobutyl Ketone solvate of Lenvatinib Mesylate.

2. A Crystalline Methyl Isobutyl Ketone solvate of Lenvatinib Mesylate.

3. The Crystalline Methyl Isobutyl Ketone solvate of Lenvatinib Mesylate according to claim 2 , having an X-ray diffraction pattern comprising peaks at about 6.80, 15.92, 25.07, 26.41 and 29.04±0.20 degrees 2-theta.

4. The Crystalline Methyl Isobutyl Ketone solvate of Lenvatinib Mesylate according to claim 3 , having an X-ray diffraction pattern comprising further peaks at 8.30, 10.70, 11.64, 19.26, 19.83, 20.86 and 21.51±0.20 degrees 2-theta.

5. The Crystalline Methyl Isobutyl Ketone solvate of Lenvatinib Mesylate according to claim 2 , having an X-ray diffraction pattern as shown in FIG. 1 .

6. A process for preparing crystalline Methyl Isobutyl Ketone solvate of Lenvatinib Mesylate, comprising the steps of:
a) mixing lenvatinib free base and Methyl Isobutyl Ketone;
b) mixing either concentrated methane sulphonic acid or an organic solution of methane sulphonic acid with the mixture from step (a); and
c) isolating the Methyl Isobutyl Ketone solvate of Lenvatinib Mesylate.

7. The process of claim 6 , wherein the organic solvent is Methyl Isobutyl Ketone.

8. A process for preparing crystalline Methyl Isobutyl Ketone solvate of Lenvatinib Mesylate, comprising the steps of:
a) mixing Lenvatinib Mesylate and a solvent or mixture of solvents;
b) mixing Methyl Isobutyl Ketone with the mixture from step (a); and
c) isolating the Methyl Isobutyl Ketone solvate of Lenvatinib Mesylate.

9. The process of claim 8 , wherein the solvent or mixture of solvents is selected from dimethylformamide, dimethylacetamide, N-Methyl-2-pyrrolidone, acetic acid, methanol, ethanol or mixtures thereof.

10. The Crystalline Methyl Isobutyl Ketone solvate of Lenvatinib Mesylate according to claim 3 , having an X-ray diffraction pattern as shown in FIG. 1 .

11. The Crystalline Methyl Isobutyl Ketone solvate of Lenvatinib Mesylate according to claim 4 , having an X-ray diffraction pattern as shown in FIG. 1 .

Assignees

• Dr Reddys Laboratories Ltd

Inventors

• Venkata Narasayya Saladi
• Mudapaka Vamsi Krishna
• Peddy Vishweshwar

Classifications

• C07B2200/13

  Crystalline forms, e.g. polymorphs · CPC title

• C07D215/48 Primary

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

• C07D215/00

  Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems · CPC title