Reaktion #8254

ord-d11bd3e8708b472f9e50678f20eb8f7e

Reaktionsgleichung

O=C([O-])O.[Na+]
sodium bicarbonate
Cc1cn(-c2ccc(NC(=O)OCc3ccccc3)cc2F)cn1
5-Benzyloxycarbonylamino-2-(4-methylimidazol-1-yl)fluorobenzene
[Li][CH2]CCC
n-butyllithium
CCCC(=O)OC[C@H]1CO1
(R)-glycidylbutyrate
Cc1cn(-c2ccc(N3C[C@H](CO)OC3=O)cc2F)cn1
title product
Ausbeute 33.7%
Cc1cn(-c2ccc(N3C[C@H](CO)OC3=O)cc2F)cn1
3-(3-Fluoro-4-(4-methylimidazol-1-yl)phenyl)-5(R)-hydroxymethyloxazolidin-2-one
Ausbeute 33.7%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooled to −70°
  2. 2
    workup.STIRRINGStirring
  3. 3
    workup.WAITwas continued for 16 hours
  4. 4
    Sonstigewas removed
  5. 5
    Waschenwashed well with diethyl ether

Vorschrift

5-Benzyloxycarbonylamino-2-(4-methylimidazol-1-yl)fluorobenzene (54 g, 0.166 M) was dissolved in a mixture of dry tetrahydrofuran (600 ml) and 1,3-dimethyl-2,4,5,6-tetrahydro-2(1H)-pyrimidinone (100 ml) under nitrogen, cooled to −70°, and treated with a solution of n-butyllithium (1.6 M in isohexane, 114 ml), over 30 minutes. After stirring for 30 minutes at 25–70°, a solution of (R)-glycidylbutyrate (26.35 g, 0.183 M) in dry tetrahydrofuran (50 ml) was added over 15 minutes. Stirring was continued for 16 hours allowing the temperature to rise to ambient. The mixture was treated with aqueous sodium bicarbonate (5%, 500 ml) and ethyl acetate (800 ml), and undissolved solid was removed and washed well with diethyl ether to give title product (16.3 g).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07087629B2uspto-grants-2006_08