Synthesis of two isomers of 3-amino-7α-12α-dihydroxy-5β-cholanic acid

Authors

  • D. O. Barsuk
  • S. M. Kovalenko

DOI:

https://doi.org/10.14739/2409-2932.2015.1.41342

Keywords:

Cholic Acid, Stereoisomers, 3-amino-7α-12α-dihydroxy-5β-cholanic acid

Abstract

Aim.With the aim of differences investigation in physical-chemical properties optimized synthesis of the two stereoisomers of 3-amino-7-12-dihydroxycholanic acid has been performed.

Methods and results.As the source compound natural cholic acid was used. 3α-amino-7α-12α-dihydroxy-5β-cholanic acid was obtained in high yield and low number of by-products. The yield of 3β-amino-7α-12α-dihydroxy-5β-cholanic acid was low because of steric interference and process needed additional treatment stages. Column chromatography was used for cleaning compounds. The structure was studied and confirmed by NMR method. Significant differences in signals of NMR spectra and physical-chemical properties 3β-amino-7α-12α-dihydroxy-5β-cholanic acid and 3α-amino-7α-12α-dihydroxy-5β-cholanic acid wasn’t found or observed.

References

Manta, J. &Lupea, V. (1937) Resynthesis of bile acids.Bull. Soc. Chim. Biol., 19, 1343.

Chang, F.C., Wood, N.F.,&Holton, W.G. (1965) 3β,12β-Dihydroxycholanic Acid.J. Org. Chem, 30(6), 1718–1723.doi: 10.1021/jo01017a004.

Ebersole, R.C. &Chang, F.C. (1999) Improved synthesis of 12-substituted-5β-cholanes.J. Org. Chem., 38(15), 2713–2715.

Davis, A.P., Bonar-Law, R.P., Sanders, J.K.M. (1996) Receptors based on cholic acid.Comprehensive Supramolecular Chemistry, 4, 257–286.

Li, Y. &Dias, J.R. (1997) Dimeric and Oligiomeric Steroids.Chem. Rev., 97(1), 283–304.doi: 10.1021/cr9600565.

Perry, J. J.& Williams, R.P. (2009) Anion recognition by tripodal receptors.J. Am. Chem. Soc., 119, 1793–1794.

Broderick, S.,Davis, A.P.,&Williams, R.P. (1998) The«triamino-analogue» of methyl cholate; a facial amphiphile and scaffold with potential for combinatorial and molecular recognition chemistry. Tetrahedron Lett.,39, 6083–6086.doi 10.1016/S0040-4039(98)01254-4.

Moore, K.S.,Wehrli, S., Roder, H., Rogers, M.,Forrest, JN.Jr,McCrimmon, D.,&Zasloff, M. (1993) Squalamine: An Aminosterol antibiotic from the shark.Proc. Natl. Acad. Sci, 90(4), 1354–1358.doi: 10.1073/pnas.90.4.1354.

Lawless, L.J., Blackburn, A.G., Ayling, A.J., et. al. (2001) Steroidal guanidines as enantioselective receptors for N-acyl α-amino acids. P. 1. 3α-Guanylatedcarbamates derived from cholic acid.Perkin Trans 1.,11, 1329–1341.

Ding, B.,Tatofa, U., Orsak, T.,Chadwell, M.,&Savage, P. B. (2004) Synthesis and Characterization of Peptide-Cationic Steroid Antibiotic Conjugates.Org. Lett., 6(20), 3433–3436.doi: 10.1021/ol048845t.

Ryu, E.-H., Yan, J.,Zhong, Z.&Zhao,Y.(2006) Solvent-InducedAmphiphilic Molecular Baskets:Unimolecular Reversed Micelles with Different Size, Shape, and Flexibility. The Journal of Organic Chemistry, 71(19), 7205–7213. doi: 10.1021/jo0607663.

Zhao,Y., &Zhong, Z. (2005) OligomericCholates: AmphiphilicFoldamers with Nanometer-Sized Hydrophilic Cavitie. Journal of the American Chemical Society, 127(50), 17894–17901.

Downloads

How to Cite

1.
Barsuk DO, Kovalenko SM. Synthesis of two isomers of 3-amino-7α-12α-dihydroxy-5β-cholanic acid. Current issues in pharmacy and medicine: science and practice [Internet]. 2015Mar.3 [cited 2024Apr.26];(1). Available from: http://pharmed.zsmu.edu.ua/article/view/41342

Issue

Section

Synthesis of the biologically active compounds