HCID 178418361, compound → HCID 178480886, compound

Participants

Reaction Steps

A solution of 4-nitrobenzyl (4R,5S,6S)-6-[(lR)-1-hydroxyethyl]-4-methyl-3-[(2S, 4S)-2-(3-methyl-1-imidazolio)methyl-1-4-nitrobenzyloxycarbonyl)pyrrolidin-4-yl]thio-7-oxo -1-azabicyclo-3.2.0]hept-2-ene-2-carboxylate iodide (0.79 g) obtained in Example 3-1) in a mixture of tetrahydrofuran (50 ml) and 0.1 M phosphate buffer (pH 6.5) (50 ml) was stirred in the presence of 20 % palladium hydroxide on carbon (0.3 g) under atmospheric pressure of hydrogen at ambient temperature for 5 hours. The catalyst was removed by filtration and the filtrate was concentrated under reduced pressure to remove the tetrahydrofuran. The residual solution was washed with ethyl acetate (50 ml ×2) and the organic solvent was removed by evaporation. The equeous solution was subjected to a column chromatography on nonionic adsorption resin, "Diaion HP-20" (50 ml), washed with water, eluted with a mixture of acetone and water (1:99 V/V). The fractionscontaining the desired compound were collected and lyophilized to give (4R,5S,6S)-6-[(lR)-1-hydroxyethyl]4-methyl-3-[(2S,4S)-2-(3-[(2S,4S)-2-(3-methyl-1-imidazolio)methylpyrrolidin-4-yl]thio-7-oxo-1-azabicyclo [3.2.0]hept-2-ene-2-carboxylate (0.25 g).

Provenance & Evidence