Sodium periodate → tert-butyl 5-oxo-3-(trifluoromethyl)-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylate

HRID 2175612Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2175612
[F:1][C:2]([F:21])([F:20])[C:3]1[CH:4]=[N:5][C:6]2[CH2:7][CH2:8][N:9]([C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[CH2:10][C:11]=2[CH:12]=1.I([O-])(=O)(=O)=[O:23].[Na+]>C(Cl)(Cl)(Cl)Cl.CC#N.O.C(Cl)Cl.O.[Ru](Cl)(Cl)Cl>[O:23]=[C:10]1[N:9]([C:13]([O:15][C:16]([CH3:17])([CH3:18])[CH3:19])=[O:14])[CH2:8][CH2:7][C:6]2[N:5]=[CH:4][C:3]([C:2]([F:20])([F:1])[F:21])=[CH:12][C:11]1=2

Komponenten

7

Versuchsvorschrift

Into a 250 mL round-bottom flask, was placed a solution of tert-butyl 3-(trifluoromethyl)-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylate (as prepared in the previous step, 3.84 g, 0.01 mol, 1.00 equiv) in CCl4/CH3CN=10/1 (66 mL), a solution of sodium periodate (8.135 g, 38.01 mmol, 3.00 equiv) in water (20 mL) and Ruthenium(III)Chloride Hydrate (0.992 g, 0.30 equiv). The resulting solution was stirred for 12 h at room temperature, and then the mixture was diluted with 50 mL of CH2Cl2. The solids were filtered out. The filtrate was concentrated under vacuum. The residue was purified by chromatography over a silica gel column with ethyl acetate/petroleum ether (1:50-1:10). The title compound was obtained as a white solid.

Aufarbeitung

  1. customInto a 250 mL round-bottom flask, was placed
  2. filtrationThe solids were filtered out
  3. concentrationThe filtrate was concentrated under vacuum
  4. customThe residue was purified by chromatography over a silica gel column with ethyl acetate/petroleum ether (1:50-1:10)

Quellen und Nachweise

ORD-Eintrag
ord-6ead46e23c774bfbbd4d14bbb962ff60
Quelldatensatz
uspto-grants-2015_06
Patentnummer
US09062048B2

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