反应详情

温度

0 °C

To a solution of N-t-butoxycarbonyl-D-alanine (5.6 g, 30 mmol, [α]D+23° (c=2, CH3CO2H)) in anhydrous tetrahydrofuran (150 mL) under N2 at 0° C. was added N-methylmorpholine (3.0 g, 30 mmol), followed by the addition of isobutylchloroformate (3.7 mL, 30 mmol), resulting in the formation of a white solid. The resulting suspension was stirred at 0° C. for 15 minutes, and then at ambient temperature for 1 hour. A solution of (2R)-3-benzyloxy-2-(N-(4-fluorobenzyl)-amino)propanoic acid methyl ester (7.5 g, 24 mmol, in 50 mL of anhydrous tetrahydrofuran) was added to the mixture and the resulting mixture was stirred at ambient temperature. After 15 hours, the mixture was filtered through Celite (tetrahydrofuran). The filtrate was concentrated in vacuo to afford a yellow liquid, which was dissolved in ethyl acetate, washed with water and then with brine. The organic phase was separated then dried over MgSO4, filtered, and concentrated in vacuo. Purification by flash column chromatography on silica gel afforded 7.3 g (63% yield) of (2R)-3-benzyloxy-2-(N-(4-fluorobenzyl)-N-(((1S)-1-(t-butoxy-carbonylamino)ethyl)carbonyl)amino)propanoic acid methyl ester, a compound of formula (Q), as a clear oil; NMR (CDCl3) 7.4-7.2 (m, 7), 7.0 (dd, 2), 5.3 (d, 2), 4.9-4.3 (m, 5), 4.1-3.7 (m, 4), 1.6 (s, 9), 1.0 (d, 3) ppm.

1. customresulting in the formation of a white solid
2. waitat ambient temperature for 1 hour
3. stirringthe resulting mixture was stirred at ambient temperature
4. waitAfter 15 hours
5. filtrationthe mixture was filtered through Celite (tetrahydrofuran)
6. concentrationThe filtrate was concentrated in vacuo
7. customto afford a yellow liquid, which
8. washwashed with water
9. customThe organic phase was separated
10. dry with materialthen dried over MgSO4
11. filtrationfiltered
12. concentrationconcentrated in vacuo
13. customPurification by flash column chromatography on silica gel