Crystalline forms of carbapenem antibiotics and methods of preparation
View Patent ↗A process for preparing a crystalline, carbapenem monosodium salt of formula IIa: characterized by the steps a) adding about 10 to 30% of an organic solvent to an aqueous solution of the carbapenem, b) cooling the resulting solution to less than −5° C., c) adjusting the pH using a solution containing an acid in an organic solvent to give the appropriate pH for crystallization, and d) crystallizing the compound by adding methanol, and a C 2-5 alcohol at between −5 and −25° C.
1. Crystalline solvate (4R,5S,6S,8R,2′S,4′S)-3-[[2-[[(3-carboxyphenyl) amino]carbonyl]pyrrolidin-4-yl]thio]-4-methyl-6-(1-hydroxyethyl)-7-oxo 1-azabicyclo[3.2.0]hept-2-en-2-carboxylic acid monosodium salt, formula IIa, having an X-ray powder diffraction pattern of Form B in accordance with FIG. 3 .
2. A process for preparing a crystalline solvate carbapenem monosodium salt of formula IIa:
comprising the steps of:
a) adding an organic solvent selected from the group consisting methanol and/or 1-propanol to an aqueous solution containing carbapenems of formula II and 4:
and/or salt forms thereof,
b) cooling the solution to below −5° C.;
c) adjusting the pH to between about 6 and about 5 utilizing an acid;
d) crystallizing by adding to the solution from about 0.5 to about 3.0 volumes of methanol relative to the aqueous solution volume, and optionally, from about 0.5 to about 3.0 volumes of [a C 1-5 alcohol]1-propanol relative to the aqueous solution volume, thereby producing a slurry of formula IIa carbapenem crystals; and
e) [washing the formula IIa carbapenem crystals with methanol and 1-propanol and] isolating the formula IIa carbapenem crystals of Form A; and
f) washing the formula IIa carbapenem crystals of Form A with water and 2-propanol and isolating the formula IIa carbapenem crystals of Form B.
3. The process according to claim 2 , wherein the C 1-5 alcohol is selected from the group consisting of methanol, 1-propanol, 2-propanol, isopropyl alcohol, ethanol, 1-butanol, 2-butanol, isobutyl alcohol, t-butyl alcohol, 1-pentanol, 2-pentanol, 3-pentanol, isopentyl alcohol and mixtures thereof.
4. A process according to claim 2 which is conducted at a temperature of about −5° C. to about −25° C. and wherein the acid is selected from a group consisting of formic acid, acetic acid, propionic acid, and butyric acid.
5. A process according to claim 4 wherein the acid is acetic acid.
6. A process for preparing a crystalline solvate carbapenem monosodium salt of general formula IIa, Form B:
wherein Form B has an X-ray powder diffraction patter 18.48, 13.02, 11.27, 8.50, 7.51, 6.51, 6.13, 5.82, 5.13, 4.78, 4.67, 4.50, 4.24, 4.06, 3.85, 3.69, 3.63, 3.41, 3.36, 3.31, 3.22, 3.11, 2.98, 2.87, and 2.77 angstroms;
comprising:
a) adding 1-propanol to an aqueous solution containing carbapenems of formula II and 4:
and/or salt forms thereof,
b) cooling the solution to below−5° C.;
c) adjusting the pH to between about 6 and about 5 utilizing an acid;
d) crystallizing by adding to the solution from about 0.5 to about 3.0 volumes of methanol relative to the aqueous volume, and from about 0.5 to a bout 3.0 volumes of 1-propanol relative to the aqueous solution volume;
and
e) isolating the formula IIa Form A carbapenem crystals
wherein Form A has an X-ray powder diffraction pattern 18.44, 13.09, 8.43, 7.58, 6.48, 6.16, 5.55, 5.14, 4.81, 4.50, 4.26, 4.11, 4.02, 3.85, 3.69, 3.41, 3,35, 3.03, 3.25, 3.12 and 2.87 angstroms;
f) washing solids containing formula IIa Form A crystals with a mixture of water and 2-propanol to give the compound of formula IIa, Form B, wherein said mixture contains from about 5% to about 25% water (v/v).