Pyridine → (6R,9aR)-1,1-dimethyl-6-(3,4,5-trifluorophenyl)tetrahydro [1,4]oxazino[3,4-c][1,4]oxazine-3,4-dione

HRID 1677093Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1677093
[C:1](Cl)(=[O:5])[C:2](Cl)=[O:3].C(Cl)(Cl)Cl.N1C=CC=CC=1.[F:17][C:18]1[CH:19]=[C:20]([C@H:26]2[NH:31][C@@H:30]([C:32]([OH:35])([CH3:34])[CH3:33])[CH2:29][O:28][CH2:27]2)[CH:21]=[C:22]([F:25])[C:23]=1[F:24]>O>[CH3:34][C:32]1([CH3:33])[C@H:30]2[CH2:29][O:28][CH2:27][C@@H:26]([C:20]3[CH:19]=[C:18]([F:17])[C:23]([F:24])=[C:22]([F:25])[CH:21]=3)[N:31]2[C:2](=[O:3])[C:1](=[O:5])[O:35]1

Komponenten

6

Versuchsvorschrift

Under ice-cooling, oxalyl chloride (205 μL) was added dropwise into a chloroform (10 mL) solution of pyridine (2 mL) and 2-[(3R,5R)-5-(3,4,5-trifluorophenyl)morpholin-3-yl]propane-2-ol (330 mg). The reaction solution was stirred for 1 hour at the same temperature, and the resultant was stirred a further 2 hours at room temperature. Water was added to the reaction solution, and the organic layer was partitioned. The organic layer was washed with brine and dried over anhydrous magnesium sulfate, and the solvent was removed under a vacuum. The residue was purified by silica gel column chromatography (heptane/ethyl acetate), and the title compound (260 mg) was obtained. The physical property values are as follows.

Aufarbeitung

  1. temperatureUnder ice-cooling
  2. stirringthe resultant was stirred a further 2 hours at room temperature
  3. customthe organic layer was partitioned
  4. washThe organic layer was washed with brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customthe solvent was removed under a vacuum
  7. customThe residue was purified by silica gel column chromatography (heptane/ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-69c55e8f3c2f4799a82e83e290a8ac07
Quelldatensatz
uspto-grants-2011_08
Patentnummer
US08008293B2

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