Reaktion #692826

Reaktionsgleichung

Methyl 2-(2-(1-(tert-butyldimethylsilyloxy)-7-phenylheptyl)oxazol-5-yl)nicotinate

2-(1-(tert-butyldimethylsilyloxy)-7-phenylheptyl)-5-(tributylstannyl)oxazole

methyl 2-chloronicotinate

→

title compound

Ausbeute 94.0%

Methyl 2-(2-(7-phenylheptanoyl)oxazol-5-yl)nicotinate

Ausbeute 94.0%

Reaktionsbedingungen

Vorschrift

Methyl 2-(2-(1-(tert-butyldimethylsilyloxy)-7-phenylheptyl)oxazol-5-yl)nicotinate. The title compound was prepared from 2-(1-(tert-butyldimethylsilyloxy)-7-phenylheptyl)-5-(tributylstannyl)oxazole (83 mg, 0.125 mmol) and methyl 2-chloronicotinate following General Procedure A. Flash chromatography (2-10% EtOAc/hexanes) yielded the title compound as a white solid (60 mg, 94%): 1H NMR (CDCl3, 500 MHz) δ 8.80 (dd, 1H, J=6.4, 3.0 Hz), 8.02 (dd, 1H, J=10.0, 6.0 Hz), 7.72 (s, 1H), 7.39-7.32 (m, 3H), 7.25-7.23 (m, 3H), 4.91 (t, 1H, J=7.0 Hz), 4.01 (s, 3H), 2.66 (t, 2H, J=7.5 Hz), 2.03-1.91 (m, 2H), 1.74-1.68 (m, 2H), 1.46-1.35 (m, 6H), 0.96 (s, 9H), 0.17 (s, 3H), 0.05 (s, 3H); 13C NMR (CDCl3, 125 MHz) δ 168.0, 166.5, 151.5, 149.9, 145.2, 143.2, 137.5, 128.8, 128.6, 128.0, 126.4, 126.0, 122.7, 69.1, 53.3, 37.0, 36.3, 31.8, 29.6, 26.2, 26.2, 25.5, 18.6, −4.5, −4.8.

Quelle