Chiral selectors and stationary phases for separating enantiomer mixtures
View Patent ↗Chiral selectors having α-unsubstituted β-amino acid derivatives of the structure: a stationary phase for separating substance mixtures containing the chiral selector, and processes for separating mixtures of chiral substances, including enantiomers, and especially enantiomers of substances selected from β-amino acids and derivatives thereof, α-amino acids and α-hydroxy acids are provided.
1. A chiral selector for a chromatographic separation, comprising:
an α-unsubstituted β-amino acid derivative of the structure (I):
wherein
n is an integer of 1-5,
R 1 is (C 6 -C 10 )-aryl, (C 7 -C 13 )-aralkyl, (C 7 -C 10 )-heteroaralkyl, or pyridyl,
X is OH,
R 2 is CH 2 CHR 3 R 4 ,
wherein
R 3 is H or OH,
R 4 is (C 1 -C 20 )-alkyl, (C 6 -C 10 )-aryl or (C 7 -C 13 )-aralkyl, and
the chiral selector is present in predominantly one absolute configuration with respect to the C-3 carbon atom (β-carbon atom).
2. The chiral selector according to claim 1 , wherein R 1 is phenyl.
3. The chiral selector according to claim 2 , wherein n is 1 and R 4 is phenyl.
4. A stationary phase for chromatographic separation, comprising
a support material, and
the chiral selector according to claim 1 ;
wherein
the support material comprises silica gel or a monolith, and
the chiral selector is bonded adsorptively to the support material.
5. A stationary phase for chromatographic separation of substance mixtures, comprising:
a support material and
a chiral selector comprising an α-unsubstituted β-amino acid derivative of the structure
wherein
R 1 is (C 6 -C 10 )-aryl, (C 7 -C 13 )-aralkyl, (C 7 -C 10 )-heteroaralkyl, or pyridyl,
R 3 is H or OH, and
R 4 is (C 1 -C 20 )-alkyl, (C 6 -C 10 )-aryl or (C 7 -C 13 )-aralkyl,
the chiral selector is present in predominantly one absolute configuration with respect to the C-3 carbon atom (β-carbon atom), and
wherein
the substance mixture comprises enantiomers of substances selected from the group consisting of β-amino acids and derivatives thereof, α-amino acids and α-hydroxy acids.
6. The stationary phase for chromatographic separation according to claim 5 , wherein
a stereocenter optionally present in the 2′ position is or is not present in predominantly one absolute configuration.
7. The stationary phase for chromatographic separation according to claim 5 , wherein R 1 is phenyl.
8. The stationary phase for chromatographic separation according to claim 5 , wherein
R 4 is (C 4 -C 18 )-alkyl.
9. The stationary phase for chromatographic separation according to claim 8 , wherein R 4 is n-decyl.
10. The stationary phase for chromatographic separation according to claim 5 , wherein R 4 is phenyl.
11. The stationary phase for chromatographic separation according to claim 5 , wherein the chiral selector is bonded adsorptively to a support material based on silica gel or a monolith.
12. The stationary phase for chromatographic separation according to claim 11 , wherein the support material is a reversed-phase material.
13. The stationary phase for chromatographic separation according to claim 12 , wherein the reversed-phase material is one RP material selected from the group consisting of RP-2, RP-4, RP-5, RP-6, RP-8, RP-12 and RP-18 phases.
14. A process for preparing the stationary phase for chromatographic separation according to claim 5 , comprising:
(i) preparing an N-alkylated amino acid, and
(ii) adsorptively attaching the N-alkylated amino acid to a support material.
15. A process for chromatographically separating substance mixtures, comprising:
contacting a solution of the substance mixture to be separated with the stationary phase for chromatographic separation according to claim 5 ;
passing a mobile phase comprising divalent transition metal ions, through the stationary phase to effect separation of mixture components on the basis of their different interaction with the stationary phase, and optionally,
isolating the separated components from the mobile phase, detecting the separated components or detecting and quantifying the components;
wherein
the substance mixture comprises a mixture of chiral substances.
16. The process according to claim 15 , wherein the substance mixture comprises enantiomers of substances selected from the group consisting of β-amino acids and derivatives thereof, α-amino acids and α-hydroxy acids.
17. The process according to claim 15 , wherein the substance mixture comprises trace amounts of enantiomers.
18. The process according to claim 17 , wherein the enantiomers comprise enantiomers of α- and β-amino acids.
19. The process according to claim 15 , wherein the divalent transition metal ion is copper(II) ion.