Fosaprepitant dimeglumine intermediate, neutral fosaprepitant, and amorphous fosaprepitant dimeglumine and processes for their preparations
The present invention generally relates to a process for the preparation of fosaprepitant dimeglumine intermediate and its use in the preparation of fosaprepitant dimeglumine; to a neutral form of fosaprepitant in a solid state and processes for the preparation thereof; and to a stable amorphous fosaprepitant dimeglumine, having a stability at temperatures of about 2° C. to about 8° C. and at a relative humidity below at least 60%; and a process for the preparation thereof.
1. A process for the preparation of dibenzyl{3-[2(R)-[(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethoxy]-3(S)-(4-fluorophenyl)morpholin-4-yl}-5-oxo-4,5-dihydro-[1,2,4]-triazol-1-yl}phosphonic acid of formula (II),
the process comprising:
a) providing a solution of dibenzyl {3-[2(R)-[(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethoxy]-3(S)-(4-fluorophenyl)morpholin-4-yl}-5-oxo-4,5-dihydro-[1,2,4]-triazolyl}phosphonic acid in a solvent or a mixture of solvents;
b) adding an anti-solvent to the solution of (a);
c) recovering dibenzyl {3-[2(R)-[(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethoxy]-3(S)-(4-fluorophenyl)morpholin-4-yl}-5-oxo-4,5-dihydro-[1,2,4]-triazol-1-yl}phosphonic acid as a crystalline compound.
2. An isolated solid crystalline dibenzyl {3-[2(R)-[(1R)-1-[3,5-bis (trifluoromethyl)phenyl]ethoxy]-3(S)-(4-fluorophenyl) morpholin-4-yl}-5-oxo-4,5-dihydro-[1,2,4]-triazol-1-yl}phosphonic acid of formula (II)
3. An isolated dibenzyl {3-[2(R)-[(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethoxy]-3(S)-(4-fluorophenyl) morpholin-4-yl}-5-oxo-4,5-dihydro-[1,2,4]-triazol-1-yl}phosphonic acid of formula (II) in crystalline form and characterized by an X-ray diffraction powder pattern with peaks at about: 3.8, 7.5, 15.0, 16.9, 17.3, 17.6, 19.3, 20.6, 21.2, 23.9, and 24.8+0.2 degrees 2 theta
4. The compound of claim 3 , having less than about 0.5 area % of monobenzyl {3-[2(R)-[(1R)-1[3,5-bis(trifluoromethyl)phenyl]-ethoxy]-3(S)-(4-fluorophenyl)morpholin-4-yl}-5-oxo-4,5-dihydro-[1,2,4]-triazol-1-yl}phosphonic acid of formula (III), as measured by high performance liquid chromatography
5. The process of claim 1 , wherein the solvent or mixture of solvents is selected from the group consisting of ethyl acetate, n-propyl acetate, isopropyl acetate, n-butyl acetate, isobutyl acetate, tertiary butyl acetate and mixtures thereof.
6. The process of claim 1 , wherein the ratio of the dibenzyl {3-[2(R)-[(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethoxy]-3(S)-(4-fluorophenyl)morpholin-4-yl}-5-oxo-4,5-dihydro-[1,2,4]-triazolyl}phosphonic acid to the solvent is about 1:2 to 1:10.
7. The process of claim 1 , wherein the anti-solvent is selected from the group consisting of n-pentane, n-hexane, n-heptane, cyclohexane or mixtures thereof.
8. The process of claim 1 , wherein the ratio of the anti-solvent to the solution of (a) is about 1:4 to 1:10.
9. The process of claim 1 , wherein the crystalline form of dibenzyl{3-[2(R)-[(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethoxy]-3(S)-(4-fluorophenyl) morpholin-4-yl}-5-oxo-4,5-dihydro-[1,2,4]-triazol-1-yl}phosphonic acid is characterized by an X-ray powder diffraction pattern with peaks at about: 3.8, 7.5, 15.0, 16.9, 17.3, 17.6, 19.3, 20.6, 21.2, 23.9, and 24.8+0.2 degrees 2 theta.
10. The process of claim 9 , wherein the crystalline form of dibenzyl {3-[2(R)-[(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethoxy]-3(5]-(4-fluorophenyl) morpholin-4-yl}-5-oxo-4,5-dihydro-[1,2,4]-triazol-1-yl}phosphonic acid is characterized by having an X-ray powder diffraction pattern, which is substantially in accordance with FIG. 1 .
11. The process of claim 1 , further comprising the step of drying the crystalline compound.
12. The compound of claim 2 characterized by having an X-ray powder diffraction pattern, which is substantially in accordance with FIG. 1 .