Process of making regadenoson and novel polymorph thereof
Novel processes for making the N-pyrrazole substituted 2-adenosine derivative regadenoson and a novel polymorph thereof. The novel polymorph of regadenoson designated form H and drug substances and pharmaceutical compositions including the novel polymorph H are disclosed.
1. A process for making a polymorph of regadenoson comprising azeotropically distilling a compound of Formula (I)
in a solvent, wherein the solvent is n-butanol, and wherein the polymorphic form is polymorphic form (H) and is characterized by:
a powder x-ray diffraction (XRPD) spectrum comprising peaks at the following angles: 6.16, 10.31, 10.72, and 25.52, ±0.2 (°2θ), measured with a Cu-Ku irradiation, and further comprising one or more peaks at the following angles: 12.38, 16.37, 21.57, 26.28, and 27.76±0.2 (°2θ), measured with a Cu-Ku irradiation; and
a differential scanning calorimetry (DSC) peak in the range of 265-280° C. measured with a heating rate of 10° C./min.
2. The process according to claim 1 wherein the distillation is conducted at a temperature in the range of 80-120° C.
3. A process for making a polymorph of regadenoson comprising recrystallizing a compound of Formula (I)
using ammoniacal methanol wherein the polymorphic form is polymorphic form (H) and is characterized by:
a powder x-ray diffraction (XRPD) spectrum comprising peaks at the following angles: 6.16, 10.31, 10.72, and 25.52, ±0.2 (°2θ), measured with a Cu-Ku irradiation, and further comprising one or more peaks at the following angles: 12.38, 16.37, 21.57, 26.28, and 27.76±0.2 (°2θ), measured with a Cu-Ku irradiation; and
a differential scanning calorimetry (DSC) peak in the range of 265-280° C. measured with a heating rate of 10° C./min.
4. The process according to claim 3 wherein the recrystallization is conducted at a temperature in the range of 0-64° C.
5. A polymorphic form of regadenoson prepared by stirring a solution or suspension of regadenoson in a water-immiscible solvent while removing water from the regadenoson solution or suspension,
wherein the polymorphic form is polymorphic form (H) and is characterized by:
a powder x-ray diffraction (XRPD) spectrum comprising peaks at the following angles: 6.16, 10.31, 10.72, and 25.52, ±0.2 (°2θ), measured with a Cu-Ku irradiation, and further comprising one or more peaks at the following angles: 12.38, 16.37, 21.57, 26.28, and 27.76±0.2 (°2θ), measured with a Cu-Ku irradiation; and
a differential scanning calorimetry (DSC) peak in the range of 265-280° C. measured with a heating rate of 10° C./min, and
wherein the water-immiscible solvent is n-butanol.
6. The polymorphic form of regadenoson prepared according to the method of claim 5 , wherein the water is removed via azeotrope with the water-immiscible solvent.
7. The polymorphic form of regadenoson prepared according to the method of claim 5 , wherein the regadenoson solution or suspension is heated to a temperature of 80-120° C.
8. A polymorphic form of regadenoson prepared by stirring regadenoson with a solution of ammonia in methanol, wherein the polymorphic form is polymorphic form (H) and is characterized by:
a powder x-ray diffraction (XRPD) spectrum comprising peaks at the following angles: 6.16, 10.31, 10.72, and 25.52, ±0.2 (°2θ), measured with a Cu-Ku irradiation, and further comprising one or more peaks at the following angles: 12.38, 16.37, 21.57, 26.28, and 27.76±0.2 (°2θ), measured with a Cu-Ku irradiation; and
a differential scanning calorimetry (DSC) peak in the range of 265-280° C. measured with a heating rate of 10° C./min.
9. The polymorphic form of regadenoson prepared according to the method of claim 8 , wherein the regadenoson solution or suspension is stirred at a temperature in the range of 0-64° C.