p-Toluenesulfonyl azide → HCID 86755102, compound

Participants

Reaction Steps

A solution of 4-methoxybenzyl 3-oxo-5-[(3SR,4RS)-3-phenylacetamidoazetidin-2-on-4-yl]pentanoate (1.38 g, 3.15 mmol) [prepared by the method described for 4-nitrobenzyl 3-oxo-5-[(3SR,4RS)-3-phenoxyacetamidoazetidin-2-on-4-yl]pentanoate, C. Bodurow and M. A. Carr, Tetrahedron Lett., 1989, 30, 4801] in acetonitrile (60 ml) was treated with 4-toluenesulphonyl azide (870 mg, 4.42 mmol) and N,N-diisopropylethylamine (822 μl, 4.73 mmol) at 0° C. After 10 min., the ice-bath was removed and stirring was continued at room temperature for 2 h. The reaction mixture was diluted with ethyl acetate and washed with brine. After drying over MgSO4, the solvent was evaporated in vacuo and the residue purified by chromatography on silica gel eluting with-ethyl acetate to yield the title compound (1.279, 87%); νmax (KBr) 2134, 1775, 1717, 1654, 1513 and 1304 cm-1 ; δH (CDCl3, 250 MHz) 1.59-1.70 (2H,m), 2.68-2.95 (2H,m), 3.55 and 3.65 (2H, ABq, J 15.6 Hz), 3.78 (1H,m), 3.82 (3H,s), 5.19 (2H,s), 5.25 (1H, ddd, J 8.1, 4.9, 1.0 Hz), 6.25 (1H, br s, exch.), 6.49 (1H, br d, J 8.1 Hz, exch.), 6.90 (2H,d, J 8.7 Hz) and 7.23-7.70 (7H,m). [Mass spectrum: +ve ion (3-nitrobenzyl alcohol, sodium acetate) MNa+ (487)].

Provenance & Evidence