反应详情

2,2′-Anhydro-5-methyluridine (17.02 g, 70.6 mmol), methanethiol (16.3 g, 339 mmol), 1,1,3,3-tetramethylguanidine (40.6 g, 353 mmol) and DMF (150 mL) were heated at 60° C. After 12 hours, the products were cooled and concentrated under reduced pressure. The residual oil was purified by short silica gel column chromatography (300 g). Pooling and concentrating appropriate fractions, which were eluted with CH2Cl2—MeOH (93:7), furnished the title compound as a white foam (15.08 g, 74.1%), which was crystallized from EtOH—CH2Cl2 as white needles.

1. temperaturethe products were cooled
2. concentrationconcentrated under reduced pressure
3. customThe residual oil was purified by short silica gel column chromatography (300 g)
4. concentrationPooling and concentrating appropriate fractions, which
5. washwere eluted with CH2Cl2—MeOH (93:7)