Dimethyl Sulfoxide → (3R,4S,5R)-3-Azido-4,5-bis-methanesulfonyloxy-cyclohex-1-enecarboxylic acid ethyl ester

A 5 mL round-bottom flask equipped with a magnetic stirrer and an inert gas supply was charged with 436.3 mg of 12 and 0.83 mL DMSO. To the clear colorless solution at RT was added 71.5 mg sodium azide and the reaction mixture was stirred for 2.5 h, then an additional 13.7 mg of sodium azide were added and stirring continued at RT for 19 h. The reaction mixture was diluted with 5 mL of EtOAc and extracted three times with a 1 M solution of NaHCO3. The organic phase was separated, dried (Na2SO4), filtered and evaporated at 20° C./140-10 mbar to obtain 0.33 g of the crude product as light yellow oil. The crude product was purified by SiO2 column chromatography eluting with a ½ mixture of EtOAc and n-hexane. The combined fractions were evaporated and dried on a rotary evaporator to obtain 0.27 g of 14 as a colorless oil

1. customA 5 mL round-bottom flask equipped with a magnetic stirrer
2. stirringstirring
3. waitcontinued at RT for 19 h
4. extractionextracted three times with a 1 M solution of NaHCO3
5. customThe organic phase was separated
6. dry with materialdried (Na2SO4)
7. filtrationfiltered
8. customevaporated at 20° C./140-10 mbar
9. customto obtain 0.33 g of the crude product as light yellow oil
10. customThe crude product was purified by SiO2 column chromatography
11. washeluting with a ½ mixture of EtOAc and n-hexane
12. customThe combined fractions were evaporated
13. customdried on a rotary evaporator

ORD-Eintrag

ord-e3e4b0a6579f43dc8853fe5088c4e146

Quelldatensatz

uspto-grants-2009_05

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07531687B2