反应详情

温度

25 °C

To a solution of 5-chloro-3-formyl-2H-chromene-2-carboxylic acid ethyl ester (1.5 g, 5.62 mmol) (from Example 1, Step 1) in methanol (20 mL) containing molecular sieves (0.7 g) was added commercially available (S)-2-amino-4-methyl-pentanoic acid methyl ester (1.2 g, 5.62 mmol) and N,N′-diisopropylethylamine (2 mL, 11.24 mmol). The mixture was stirred at 25° C. for 10 hours. At this time, sodium cyanoborohydride (0.706 g, 11.24 mmol) and acetic acid (0.70 mL, 11.24 mmol) were added simultaneously to the reaction mixture, and the reaction mixture was stirred for additional 16 hours at 25° C. The reaction mixture was then filtered through celite and washed with methanol. The filtrate was concentrated in vacuo and the residue was purified using flash column chromatography over neutral alumina (eluant-ethyl acetate:petroleum ether 1:19, Rf=0.7) to afford 5-chloro-3-[((S)-1-methoxycarbonyl-3-methyl-butylamino)-methyl]-2H-chromene-2-carboxylic acid methyl ester (1.2 g, 54.5%) as an oil.

1. stirringthe reaction mixture was stirred for additional 16 hours at 25° C
2. filtrationThe reaction mixture was then filtered through celite
3. washwashed with methanol
4. concentrationThe filtrate was concentrated in vacuo
5. customthe residue was purified