Processes for the preparation of multicomponent crystalline forms of active pharmaceutical ingredients using solvent vapour

Patent metadata

Field	Value
Publication number	US-12583860-B2
Application number	US-202117802203-A
Country	US
Kind code	B2
Filing date	Feb 24, 2021
Priority date	Feb 26, 2020
Publication date	Mar 24, 2026
Grant date	Mar 24, 2026

Abstract

The present invention provides solvent-limited processes for the preparation of an existing crystalline solid form of an active pharmaceutical ingredient comprising mixing, in the presence of solvent vapour, of a solid active pharmaceutical ingredient and a pharmaceutically acceptable entity that is either a high-boiling liquid or a solid. Also provided is the use of a standard rotary apparatus, such as a rotary cone dryer, for application of the processes herein.

First claim

What is claimed is:

1 . A process for the preparation of an existing crystalline solid form comprising an active pharmaceutical ingredient and a distinct pharmaceutically acceptable entity, wherein the existence of the crystalline solid form has been confirmed prior to conducting the process, the process comprising mixing, in the presence of solvent vapour, of:
(i) the active pharmaceutical ingredient in solid form; and (ii) the pharmaceutically acceptable entity, in solid or liquid form, wherein the entity has a melting point greater than approximately 30° C. or a boiling point greater than approximately 150° C. and the pharmaceutically acceptable entity and active pharmaceutical ingredient are incorporated in the same crystalline lattice, wherein the mixing is conducted in a rotary apparatus by means of rotation of a vessel containing the active pharmaceutical ingredient and the entity about its own axis, wherein the rotary apparatus comprises: a fixed support structure; a vessel rotatably supported by the fixed support structure about an axis and defining a chamber for mixing of the active pharmaceutical ingredient and the entity; an aperture in the vessel enabling communication between the chamber and a source of solvent vapour; and means for rotating the vessel about the axis.

2 . The process of claim 1 , wherein the solvent vapour is delivered through a first aperture in the vessel and evacuated through a second aperture in the vessel that is spaced from the first aperture.

3 . The process of claim 1 , wherein the entity is a coformer and the crystalline solid form is a multiple-component crystalline form.

4 . A process for the preparation of an existing crystalline solid form comprising an active pharmaceutical ingredient and a distinct pharmaceutically acceptable entity, wherein the existence of the crystalline solid form has been confirmed prior to conducting the process, the process comprising mixing, in the presence of solvent vapour, of:
(i) the active pharmaceutical ingredient in solid form; and (ii) the pharmaceutically acceptable entity, in solid or liquid form, wherein the entity has a melting point greater than approximately 30° C. or a boiling point greater than approximately 150° C. and the pharmaceutically acceptable entity and active pharmaceutical ingredient are incorporated in the same crystalline lattice, wherein the entity is an acid and the crystalline solid form is a salt, wherein the active pharmaceutical ingredient is an amine and the acid has a melting point greater than approximately 30° C., and wherein the acid is selected from the group consisting of fumaric acid, maleic acid, L-malic acid, succinic acid, citric acid, L-tartaric acid, oxalic acid, and naphthalene-2-sulfonic acid.

5 . The process of claim 3 , wherein the multiple-component crystalline form is selected from the group consisting of:
(i) a cocrystal of acalabrutinib and urea; (ii) a cocrystal of acalabrutinib and nicotinamide; (iii) a solvate of ibrutinib and methyl benzoate; (iv) a cocrystal of ibrutinib and methyl nicotinate; (v) a cocrystal of tetrabenazine and quercetin; (vi) a cocrystal of lesinurad and nicotinamide; and (vii) a cocrystal of lumacaftor and nicotinamide.

6 . The process of claim 5 , wherein the multiple-component crystalline form is a cocrystal of acalabrutinib and urea having a molar ratio of acalabrutinib to urea of approximately 1:2.

7 . The process of claim 5 , wherein the multiple-component crystalline form is a cocrystal of acalabrutinib and nicotinamide having a molar ratio of acalabrutinib to nicotinamide of approximately 1:2.

8 . The process of claim 5 , wherein the multiple-component crystalline form is a solvate of ibrutinib and methyl benzoate having a molar ratio of ibrutinib to methyl benzoate of approximately 1:0.5.

9 . The process of claim 5 , wherein the multiple-component crystalline form is a cocrystal of ibrutinib and methyl nicotinate having a molar ratio of ibrutinib to methyl nicotinate of approximately 1:0.5.

10 . The process of claim 5 , wherein the multiple-component crystalline form is a cocrystal of tetrabenazine and quercetin having a molar ratio of tetrabenazine to quercetin of approximately 1:1.

11 . The process of claim 4 , wherein the active pharmaceutical ingredient is remdesivir and the entity is selected from the group consisting of maleic acid, oxalic acid, and naphthalene-2-sulfonic acid.

12 . The process of claim 11 , wherein the salt is a napsylate salt of remdesivir having a molar ratio of remdesivir to naphthalene-2-sulfonic acid of approximately 1:1.

13 . The process of claim 11 , wherein the salt is a maleate salt of remdesivir.

14 . The process of claim 11 , wherein the salt is an oxalate salt of remdesivir.

Assignees

• Apotex Inc

Inventors

• Stirk Alexander J
• Souza Fabio E S
• Karadeolian Avedis
• Rey Allan W
• Mohammadpourmir Fatemeh

Classifications

• A61K31/352

  condensed with carbocyclic rings, e.g. methantheline  {(cannabinoids A61K31/658)} · CPC title

• C07D471/04

  Ortho-condensed systems · CPC title

• C07D311/30

  not hydrogenated in the hetero ring, e.g. flavones · CPC title

• C07D213/82

  in position 3 · CPC title

• C07C275/02

  Salts; Complexes; Addition compounds · CPC title