Citric Acid → Ethyl[5-(3,5-difluorophenyl)-5-methyl-2,4-dioxo-3-pyridin-2-ylimidazolidin-1-yl]acetate

HRID 1685382Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1685382
[CH2:1]([O:3][C:4](=[O:22])[CH2:5][N:6]1[C:10]([C:12]2[CH:17]=[C:16]([F:18])[CH:15]=[C:14]([F:19])[CH:13]=2)([CH3:11])[C:9](=[O:20])[NH:8][C:7]1=[O:21])[CH3:2].[NH2:23][C:24]1C=[CH:28][CH:27]=[CH:26][CH:25]=1.BrC1C=CC=CN=1.C([O-])(=O)C.[K+].C(O)(=O)CC(CC(O)=O)(C(O)=O)O>N1C=CC=CC=1.[Cu].[Cu]Cl.CCOC(C)=O>[CH2:1]([O:3][C:4](=[O:22])[CH2:5][N:6]1[C:10]([C:12]2[CH:17]=[C:16]([F:18])[CH:15]=[C:14]([F:19])[CH:13]=2)([CH3:11])[C:9](=[O:20])[N:8]([C:28]2[CH:27]=[CH:26][CH:25]=[CH:24][N:23]=2)[C:7]1=[O:21])[CH3:2]

Komponenten

10

Versuchsvorschrift

A stirred solution of ethyl[5-(3,5-difluorophenyl)-5-methyl-2,4-dioxoimidazolidin-1-yl]acetate, isomer A (100 mg, 0.320 mmol, described in Intermediate 7), 2-bromopyridine (0.156 mL, 1.60 mmol), copper powder (71.2 mg, 1.12 mmol), copper (I) chloride (6.34 mg, 0.064 mmol), and potassium acetate (94.0 mg, 0.961 mmol) in pyridine (1.8 mL) was heated at 100° C. for 18 h. The cooled reaction mixture was poured onto 10% citric acid (20 mL) and with EtOAc (3×20 mL). The combined organic extracts were dried over Na2SO4, filtered and concentrated under reduced pressure. The crude product was purified by silica gel chromatography, eluting with a gradient of hexane:EtOAc—100:0 to 50:50, to provide the title compound. MS: m/z=390 (M+1).

Aufarbeitung

  1. customThe cooled reaction mixture
  2. dry with materialThe combined organic extracts were dried over Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated under reduced pressure
  5. customThe crude product was purified by silica gel chromatography
  6. washeluting with a gradient of hexane

Quellen und Nachweise

ORD-Eintrag
ord-cfcf6faedb6b4c98a25f17fd6a0d0008
Quelldatensatz
uspto-grants-2012_04
Patentnummer
US08148390B2

Notizen zur Reaktion

Wird geladen…