反应详情

To a solution of 11.0 g (1.0 eq) (R)-dimethyl 2-(3-(2,3-dihydro-1H-inden-1-ylamino)allylidene)malonate in 80 ml dry MeOH was slowly added 3.65 g (2.5 eq) NaH (60% dispersion in mineral oil) under N2 protection. The reaction was stirred at room temperature for 10 minutes and was then heated at 60° C. After 20 minutes, to the reaction mixture were added 30 ml water. The resulting mixture was heated at 60° C. for an additional 20 minutes. The solvent was removed in vacuo. The residue was diluted with 50 ml water, and extracted with hexane (2×50 ml) to remove mineral oil. Then the aqueous mixture was acidified with 2N HCl to pH 1-2 and extracted with ethyl acetate (2×100 ml). The combined organic phase was washed with 100 ml brine, dried over sodium sulfate and concentrated in vacuo to afford (R)-1-(2,3-dihydro-1H-inden-1-yl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid as a white solid (8.7 g, yield 93%) which was used without further purification.

1. temperaturewas then heated at 60° C
2. waitAfter 20 minutes
3. temperatureThe resulting mixture was heated at 60° C. for an additional 20 minutes
4. customThe solvent was removed in vacuo
5. additionThe residue was diluted with 50 ml water
6. extractionextracted with hexane (2×50 ml)
7. customto remove mineral oil
8. extractionextracted with ethyl acetate (2×100 ml)
9. washThe combined organic phase was washed with 100 ml brine
10. dry with materialdried over sodium sulfate
11. concentrationconcentrated in vacuo