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O c t o b e r 1 9 - 2 0 , 2 0 1 8 | T o k y o , J a p a n
Materials Summit 2018 & Separation Summit 2018
Materials Science and Nanotechnology
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Volume 2
ADVANCED MATERIALS AND POLYMER SCIENCE
SEPARATION TECHNIQUES
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Mater Sci Nanotechnol 2018, Volume 2
ENANTIO-RESOLUTION OF (+)- BUPROPION BY REVERSED PHASE
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY USING CYANURIC
CHLORIDE BASED CHIRAL DERIVATIZING REAGENTS HAVING AMINO
ACIDS AS CHIRAL AUXILIARIES
Sonika Batra
and
Ravi Bhushan
GD Goenka University, India
E
nantio-separation of (+)- bupropion was achieved as its diastereomers which were prepared with chiral derivatizing reagents
(CDRs) synthesized from cyanuric chloride. Two sets of CDRs each consisting of five CDRs were prepared by nucleophilic
substitution of Cl atom in cyanuric chloride with amino acids (namely, L Leu, L Val, L Phe, D Phg and L Ala) as chiral auxiliaries
to give dichloro-s-triazine (DCT) and other five new CDRs were prepared by nucleophilic substitution of Cl atom in 6 butoxy
derivative of cyanuric chloride with the above mentioned amino acids. The diastereomers were synthesized under microwave
irradiation for 70 or 90s at 80% power and by conventional heating method. Separation of diastereomers was achieved using C
18
column and an isocratic eluting mixture of acetonitrile and aqueous trifluoroacetic acid. Separation efficiencies of the two sets
of CDRs, among themselves and among the two groups, have been compared based on resolution (Rs) and difference between
the retention times of resolved diastereomers. The method was validated for detection limit, linearity, accuracy and precision.
sonikabatra211@gmail.com