Benzyl Bromide → 5-Acetyl-1,3-dibenzyluracil

HRID 2099237Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2099237
[C:1]([C:4]1[C:5](=O)[NH:6][C:7](=[O:10])[NH:8][CH:9]=1)(=[O:3])[CH3:2].[C:12](=[O:15])([O-])[O-].[K+].[K+].[CH2:18](Br)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>CN(C=O)C>[C:1]([C:4]1[C:12](=[O:15])[N:8]([CH2:9][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[C:7](=[O:10])[N:6]([CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH:5]=1)(=[O:3])[CH3:2]

Komponenten

5

Edukt 3

HCID 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 2345815-Acetyluracil

Produkt 1

HCID 116744085-Acetyl-1,3-dibenzyluracilAusbeute 79,9 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

A suspension of 5-acetyluracil (3.1 g, 20 mmol), and potassium carbonate (6.9 g, 50 mmol) in DMF (75 ml) was stirred for 20 min. Then benzyl bromide (6.0 ml, 50 mmol) was added. The resulting mixture was stirred for 8 h at room temperature. DMF was distilled under vacuum. The residue was purified by column (dichloromethane:methanol 40:1). The appropriate fraction was concentrated and crystallized from ethanol to afford 5.34 g of a white solid. Yield was 79.8%. Mp. 92-93° C. 1HNMR (CDCl3): 8.23 (s, 1H), 7.29-7.49 (m, 10H), 5.17 (s, 2H), 5.01 (s, 2H), 2.62 (s, 3H). 13CNMR (CDCl3): 194.5, 160.7, 151.0, 148.4, 136.2, 134.4, 129.2, 129.0, 128.9, 128.5, 128.2, 127.8, 112.2, 53.4, 44.9, 30.7. FAB-HRMS: [M+H]+ Calcd. for C20H19N2O3 335.1396. Found 335.1412.

Aufarbeitung

  1. stirringThe resulting mixture was stirred for 8 h at room temperature
  2. distillationDMF was distilled under vacuum
  3. customThe residue was purified by column (dichloromethane:methanol 40:1)
  4. concentrationThe appropriate fraction was concentrated
  5. customcrystallized from ethanol

Quellen und Nachweise

ORD-Eintrag
ord-b63df88513e4478988819180560472a1
Quelldatensatz
uspto-grants-2009_08
Patentnummer
US07569573B2

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