Reaktion #44611

ord-5751d1605b924848abd1cef897baba5b

Reaktionsgleichung

O=S([O-])O.[Na+]
sodium hydrogensulfite
[Na+].[OH-]
sodium hydroxide
OO
hydrogen peroxide
CCC(C)[BH-](C(C)CC)C(C)CC.[Li+]
lithium tri-sec-butyl borohydride
C[C@H]1CN([C@H](c2cc(F)c(F)c(F)c2)[C@@H](C)O[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)C(=O)C(=O)O1
(S)-4-[(1R,2R)-2-tert-butyldiphenylsilanyloxy-1-(3,4,5-trifluorophenyl)propyl]-6-methylmorpholin-2,3-dione
CC1CN([C@H](c2cc(F)c(F)c(F)c2)[C@@H](C)O[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)C(=O)[C@@H](O)O1
title compound
Ausbeute 97.5%
CC1CN([C@H](c2cc(F)c(F)c(F)c2)[C@@H](C)O[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)C(=O)[C@@H](O)O1
(S)-4-[(1R,2R)-2-tert-butyldiphenylsilanyloxy-1-(3,4,5-trifluorophenyl)propyl]-2-hydroxy-6-methylmorpholin-3-one
Ausbeute 97.5%

Lösungsmittel

Reaktionsbedingungen

Temperatur
-20°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGThis reaction solution was stirred under ice-
  2. 2
    Temperaturcooling for 1 hr
  3. 3
    workup.STIRRINGthis reaction solution was stirred at room temperature for 30 min
  4. 4
    SonstigeThe organic layer was separated
  5. 5
    Waschenwashed with saturated saline
  6. 6
    Trocknendried over anhydrous magnesium sulfate
  7. 7
    Einengenconcentrated under reduced pressure
  8. 8
    SonstigeThe obtained residue was purified by silica gel column chromatography (eluting solvent; heptane ethyl acetate=1:1)

Vorschrift

In nitrogen atmosphere, a THF solution (0.25 mL) of 1.06 M lithium tri-sec-butyl borohydride was dropwise added to a THF solution (3 mL) of (S)-4-[(1R,2R)-2-tert-butyldiphenylsilanyloxy-1-(3,4,5-trifluorophenyl)propyl]-6-methylmorpholin-2,3-dione (95 mg) at −20° C. This reaction solution was stirred at −20° C. for 30 min. To this reaction solution, a 5 N sodium hydroxide aqueous solution (0.03 mL) and a 30% hydrogen peroxide aqueous solution (0.07 mL) were added. This reaction solution was stirred under ice-cooling for 1 hr. A sodium hydrogensulfite powder (20 mg) was added to the reaction solution, and this reaction solution was stirred at room temperature for 30 min. To this reaction solution, saturated saline and ethyl acetate were added. The organic layer was separated, washed with saturated saline, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluting solvent; heptane ethyl acetate=1:1) to give 93 mg of the title compound. The physical property values of this compound were as follows:

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07737141B2uspto-grants-2010_06