Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
The present disclosure relates to processes for preparing (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide, solid state forms thereof, and corresponding pharmaceutical compositions, methods of treatment (including treatment of rheumatoid arthritis), kits, methods of synthesis, and products-by-process.
1. An extended release pharmaceutical tablet comprising:
(a) 15 mg of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide;
(b) an acidic pH modifier; and
(c) a release control polymer.
2. The tablet of claim 1 , wherein the release control polymer is a hydrophilic polymer and wherein the acidic pH modifier is an organic acid.
3. The tablet of claim 2 , wherein the organic acid is present in an amount from about 10 w/w % to about 35 w/w %.
4. The tablet of claim 3 , wherein the organic acid is tartaric acid.
5. The tablet of claim 2 , wherein the extended release formulation provides for the release of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide upon entry into a use environment at a rate substantially independent of the pH of the use environment, wherein the use environment has a pH range from about 1.2 to about 6.8.
6. The tablet of claim 5 , wherein the organic acid is present in an amount from about 10 w/w % to about 35 w/w %.
7. The tablet of claim 6 , wherein the organic acid is tartaric acid.
8. The tablet of claim 2 , wherein the extended release solid dosage form, when added to a test medium comprising 900 mL of 50 mM pH 6.8 sodium phosphate buffer at 37° C.±0.5° C. in a standard USP rotating paddle apparatus when the paddles are rotated at 75 rpm±4%, dissolves from about 50% to about 90% of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide after about 8 hours.
9. The tablet of claim 8 , wherein the organic acid is present in an amount from about 10 w/w % to about 35 w/w %.
10. The tablet of claim 9 , wherein the organic acid is tartaric acid.