反应详情

To a solution of 0.25 g (0.82 mmol) (4R,9aR)-6-hydroxy-4-methyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester in 2 ml N,N-dimethylformamide, 40 mg (0.90 mmol) sodium hydride (55–65% dispersion in oil) was added. After 30 min, 0.10 ml (0.23 g, 1.64 mmol) methyl iodide was added. After 1 h the reaction mixture was poured onto water and extracted three times with ethyl acetate. The organic layers were washed twice with water, then brine and were dried over magnesium sulfate. After filtration and evaporation of the solvent the product was purified by column chromatography on silica gel (0.032–0.063 mm) with ethyl acetate:n-hexane (1:5) as eluant.

1. additionAfter 1 h the reaction mixture was poured onto water
2. extractionextracted three times with ethyl acetate
3. washThe organic layers were washed twice with water
4. dry with materialbrine and were dried over magnesium sulfate
5. filtrationAfter filtration and evaporation of the solvent the product
6. customwas purified by column chromatography on silica gel (0.032–0.063 mm) with ethyl acetate:n-hexane (1:5) as eluant