Water → 6-nitro-2,2-dimethyl-3-(trifluoroacetamido)methyl-4-(2-oxo-1,2-dihydropyridin-1-yl)-2H-1-benzopyran

HRID 2399331Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2399331
[N+:1]([C:4]1[CH:5]=[CH:6][C:7]2[O:12][C:11]([CH3:14])([CH3:13])[C:10](O)([CH2:15][NH:16][C:17](=[O:22])[C:18]([F:21])([F:20])[F:19])[CH:9]([N:24]3[CH:29]=[CH:28][CH:27]=[CH:26][C:25]3=[O:30])[C:8]=2[CH:31]=1)([O-:3])=[O:2].[H-].[Na+].O.C(OCC)(=O)C>O1CCCC1>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]2[O:12][C:11]([CH3:13])([CH3:14])[C:10]([CH2:15][NH:16][C:17](=[O:22])[C:18]([F:21])([F:19])[F:20])=[C:9]([N:24]3[CH:29]=[CH:28][CH:27]=[CH:26][C:25]3=[O:30])[C:8]=2[CH:31]=1)([O-:3])=[O:2]

Komponenten

6

Versuchsvorschrift

A solution of 6-nitro-2,2-dimethyl-3-hydroxy-3,4-dihydro-3-(trifluoroacetamido)methyl-4-(2-oxo-1,2-dihydropyridin-1-yl)-2H-1-benzopyran (0.5 g, 1.13 mmol) in tetrahydrofuran (20 ml) containing sodium hydride (80%, 0.034 g, 1.13 mol) was refluxed for one hour. Water and ethyl acetate were added to the cooled solution and the organic phase was separated and evaporated under reduced pressure. The residue was chromatographed on silica gel, eluting with dichloromethane/acetone (95/5), to give 0.13 g of 6-nitro-2,2-dimethyl-3-(trifluoroacetamido)methyl-4-(2-oxo-1,2-dihydropyridin-1-yl)-2H-1-benzopyran, m.p. 189° C.

Aufarbeitung

  1. temperaturewas refluxed for one hour
  2. customthe organic phase was separated
  3. customevaporated under reduced pressure
  4. customThe residue was chromatographed on silica gel
  5. washeluting with dichloromethane/acetone (95/5)

Quellen und Nachweise

ORD-Eintrag
ord-523755b69ab0494aa62934a5bd6838cf
Quelldatensatz
uspto-grants-1995_09
Patentnummer
US05447943

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