Ozone → HCID 10310975, compound

Participants

Reaction Conditions

Reaction Steps

Ozone was bubbled through a solution of 393.0 mg (623.0 μmol) of 1-benzylcyclohexyl (1S)-1-[cyano(triphenylphosphoranylidene)acetyl]pentylcarbamate in 12 mL of dichloromethane at −78° C. for 15 min. The solution was purged with nitrogen for 5 min, then 80.3 μL (623.0 μmol) of (S)-α-methylbenzylamine was added and the solution was stirred at −78° C. for 15 min. The solution was concentrated and 5 mL of a 1 M solution of silver nitrate in tetrahydrofuran:water (4:1) was added and the mixture was stirred for 66 h at room temperature. The solution was extracted with ethyl acetate. The organic layer was washed with 10% citric acid, followed by saturated sodium bicarbonate, and saturated sodium chloride. The organic layer was dried over magnesium sulfate, filtered, and concentrated. The residue was purified by silica gel column chromatography eluting with an ethyl acetate:hexanes solution (1:4) to give 115.6 mg (39%) of 1-benzylcyclohexyl(1S)-1-(oxo{[(1R)-1-phenylethyl]amino}acetyl)pentylcarbamate. Rf=0.30 (1:4 ethyl acetate:hexanes); 1H NMR (300 MHz, DMSO-d6) δ 9.18 (d, J=8 Hz, 1H), 7.36-7.06 (m, 11H), 4.98 (p, J=8 Hz, 1H), 4.82-4.74 (m, 1H), 3.10 (s, 2H), 2.01 (d, J=12 Hz, 2H), 1.80-1.10 (m, 14H), 1.42 (d, J=7 Hz, 3H), 0.82 (t, J=7 Hz, 3H); HRMS C29H38N2O4+Na m/z 501.2729 (M+Na)Cal; 501.2711 (M+Na)Obs.

Provenance & Evidence