Processes for the preparation of regadenoson and a new crystalline form thereof
View Patent ↗This disclosure relates to an improved process for the preparation of regadenoson, pharmaceutically acceptable salts thereof, and hydrates thereof, and for the preparation of intermediates useful in the synthesis of regadenoson. The disclosure also relates to a new crystalline form of regadenoson. Processes for the preparation of the crystalline form, compositions containing the crystalline form, and methods of use thereof are also described.
1. A process for the preparation of regadenoson of Formula (IA), a pharmaceutically acceptable salt thereof, or a hydrate thereof:
comprising contacting 2-fluoroadenosine of Formula (IIA) with 4-N -methylcarboxamide pyrazole of Formula (IIIA):
in the presence of a metal catalyst and a base.
2. The process of claim 1 , wherein the reaction is conducted in a solvent selected from acetonitrile, dimethylsulfoxide, and mixtures thereof.
3. The process of claim 1 , wherein the base is selected from sodium hydroxide, potassium hydroxide, 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), 1,4-diazabicyclo [2.2.2]loctane (DABCO), and combinations thereof.
4. The process of claim 3 , wherein the base is DBU.
5. The process of claim 1 , wherein the metal catalyst is a copper (II) catalyst.
6. The process of claim 5 , wherein the copper (II) catalyst is chelated to a resin.
7. The process of claim 1 , wherein the reaction is conducted at a temperature of between about 60° C. and about 90° C.
8. The process of claim 1 , wherein the regadenoson of Formula (IA) is a monohydrate.
9. The process of claim 1 , further comprising converting the regadenoson, or hydrate thereof, to a pharmaceutically acceptable salt thereof.
10. The process of claim 1 , further comprising the step of subjecting the regadenoson to reverse phase chromatography.
11. The process of claim 10 , wherein the column is eluted with water and methanol.
12. A composition comprising:
(a) regadenoson, and
(b) 2-fluoroadenosine of Formula (IIA)
in an amount up to about 0.2%, based upon the total weight of the composition.
13. A parenteral solution comprising the composition of claim 12 .
14. A crystalline form of regadenoson (Form D) having an X-Ray powder diffraction pattern substantially as shown in FIG. 4 .
15. The crystalline form of regadenoson (Form D) of claim 14 , wherein the crystalline form contains between about 0.8 and about 1.7% by weight of water of hydration.
16. A pharmaceutical composition comprising a crystalline form of claim 14 and a pharmaceutically acceptable carrier.
17. A method of preparing a parenteral solution of regadenoson comprising dissolving Form D of regadenoson of claim 14 in an aqueous solution and optionally adding one or more pharmaceutically acceptable excipients.