Реакция #1121784

ord-f79edbf0b51b4ab298bee8749f1db8a2

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    СушкаThe organic phase was dried over magnesium sulphate
  2. 2
    Другоеevaporated to a volume of ˜10 ml
  3. 3
    Другоеprecipitated with pet. ether
  4. 4
    ДругоеThe two products were separated by column chromatography
  5. 5
    ДругоеThe products was precipitated in pet. ether

Методика

6-Benzyloxypurine (4.18 g; 18.5 mmol) was added to a suspension of potasiumcarbonate (3.1 g; 22.4 mmol) in DMF (100 ml). After 15 min. bromoacetic acid methyl ester (1.93 ml; 20.4 mmol) was added. The reaction was monitored by TLC in butanol:acetic acid:water 4:1:1. Upon completion, the reaction mixture was portioned between water (600 ml) and ethylacetate (600 ml). The organic phase was dried over magnesium sulphate and evaporated to a volume of ˜10 ml and precipitated with pet. ether. The two products were separated by column chromatography using ethylacetate as the solvent. The products was precipitated in pet. ether. Yield: 2.36 g (43%). Melting point: 111.5-115° C. UV λmax=250 nm (9-alkylated); λmax=260 nm (7-alkylated). 1H-NMR (DMSO-d6): 8.60 (1H, s); 8.43 (1H, s); 7.6-7.35 (5H, m); 5.69 (2H, s); 5.26 (2H, s); 3.75 (3H, s).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08546309B2uspto-grants-2013_10