Asymmetric synthesis of rasagiline
GUO Shun-min
QI Yi-ping
LIN Sui
Abstract:Objective :To build the method of asymmetric synthesis of Rasagiline. Methods: (R) -tert-bu-tanesu-lfinamide and 1-indanone were used as the starting material. The resulted imines were reduced with NaBH4in THF to provide the corresponding secondary sulfinamides in high yield and diastereoselectivity. By series of reac-tions, rasagiline was synthesized. Results: The chemical structure of the target compound was confirmed by the melting point, NMR, MS and optical activity. Conclusion:By using (R)-tert-butanesulfinamide, rasagiline can be synthesized with high yield and good asymmetric selectivity.
Keywords:rasagilinesynthesistert-butanesulfinamide
Publication Date:2009-01-01
Online Publishing Date:2026-08-14(First online date of this platform, not the publication date of the document)
Pages:3( 1352-1353,1371 )
CHINESE JOURNAL OF NEW DRUGS

CHINESE JOURNAL OF NEW DRUGS

PKUISTIC
ISSN:1003-3734
Year, Vol.(Issue):2009,18(14)