反应详情

A suspension of 4-((1R,2R)-2-(tert-butyldimethylsilyloxy)-1-(5-(4-nitrophenyl)-1,3,4-oxadiazol-2-yl)propylamino)-2-chloro-3-methylbenzonitrile (1.6 g, 3.03 mmol), 5 wt. % Pd on activated carbon (700 mg) in CH2Cl2 (50 mL) was pressurized with 30 psi of H2 and reacted on a Parr shaker for 5 h. The reaction was filtered through Celite® under N2 and rinsed with CH2Cl2 (3×40 mL). The filtrate was concentrated under reduced pressure to provide a colourless solid (1.40 g, 93%): 1H NMR (400 MHz, CDCl3, δ in ppm) 7.76 (dm, J=8.8 Hz, 2H), 7.34 (d, J=8.6 Hz, 1H), 6.70 (dm, J=8.8 Hz, 2H), 6.62 (d, J=8.6 Hz, 1H), 5.11 (d, J=9.0 Hz, 1H), 4.79 (dd, J=3.9, 8.8 Hz, 1H), 4.41 (dq, J=3.9, 6.3 Hz, 1H), 4.05 (s, 2H), 2.32 (s, 3H), 1.28 (d, J=6.3 Hz, 3H), 0.93 (s, 9H), 0.13 (s, 3H), 0.10 (s, 3H).

1. customreacted on a Parr shaker for 5 h
2. filtrationThe reaction was filtered through Celite® under N2
3. washrinsed with CH2Cl2 (3×40 mL)
4. concentrationThe filtrate was concentrated under reduced pressure