(1R,1′R)-atracurium salts separation process
View Patent ↗The present invention provides an improved method for obtaining cisatracurium besylate, which preferably chromatographically separating cisatracurium besylate from a mixture of (1R,1′R)-atracurium isomers via flash chromatography.
1. A method of separating the 1R-cis,1′R-cis isomer (cisatarcurium) from (1R,1′R)-atracurium salt isomer mixture, the method comprising:
(a) loading the (1R,1′R)-atracurium salt isomer mixture onto a chromatographic column comprising a stationary phase suitable for normal phase flash chromatography;
(b) eluting with an eluant at low to medium pressure, to elute from the column one or more fractions comprising a cisatracurium salt, which is substantially free of other (1R,1′R)-atracurium isomers;
(c) collecting one or more of the fractions, to obtain a cisatracurium salt, which is substantially free of other (1R,1′R)-atracurium isomers;
(d) optionally performing an ion exchange; and
(e) isolating the cisatracurium salt
wherein step (b) comprises eluting with a non-aqueous mobile phase comprising a weak organic acid.
2. The method of claim 1 , wherein the non-aqueous mobile phase comprises hexane, toluene, diethyl ether, ethyl acetate, dichloromethane, chloroform, tetrahydrofuran (THF), methanol, ethanol, isopropanol, dimethylsulfoxide (DMSO), or a mixture thereof.
3. The method of claim 2 , wherein the non-aqueous mobile phase comprises dichloromethane, methanol, dimethyl sulfoxide (DMSO) or a mixture thereof.
4. The method of claim 1 , wherein the weak organic acid is formic acid, acetic acid or propionic acid.
5. The method of claim 4 , wherein the weak organic acid is acetic acid.
6. The method of claim 1 , wherein the eluant comprises dichloromethane, DMSO and acetic acid in a ratio ranging from 70-85 (volumes dichloromethane): 5-20 (volumes DMSO):5-15 (volumes acetic acid).
7. The method of claim 1 , comprising performing step (d), wherein step (d) comprises contacting an eluted material with an ion exchange resin carrying benzenesulfonate anions.
8. The method of claim 1 , wherein step (e) comprises adjusting the pH of an aqueous cisatracurium besylate solution to 3 with an aqueous benzenesulfonic acid solution.
9. The method of claim 1 , wherein step (e) comprises freeze drying or spray drying.
10. The method of claim 1 , wherein the cisatracurium salt obtained in step (e) is cisatracurium besylate having an isomeric purity of at least 97%.
11. The method of claim 10 , wherein the cisatracurium salt obtained in step (e) is cisatracurium besylate having an isomeric purity of at least 99%.
12. The method of claim 11 , wherein the cisatracurium salt obtained in step (e) is cisatracurium besylate having an isomeric purity of at least 99.5%