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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235762Generated: October 26, 2026

Diphenyl chlorophosphate → 4-nitrobenzyl(5R,6S)-3-(4-pyridylthio)-6-[1-methyl-1-(4-nitrobenzyloxycarbonyloxy)ethyl]-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate

https://huagongshe.com/reaction/235762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenyl chlorophosphateHCID 75654—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-nitrobenzyl(2R,5R,6S)-3,7-dioxo-6-[1-methyl-1-(4-nitrobenzyloxycarbonyloxy)ethyl]-1-azabicyclo[3.2.0]heptane-2-carboxylateHCID 22823193—
Reactantpyridine-4-thiolHCID 178418431—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product4-nitrobenzyl(5R,6S)-3-(4-pyridylthio)-6-[1-methyl-1-(4-nitrobenzyloxycarbonyloxy)ethyl]-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylateHCID 1860658881.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-nitrobenzyl(2R,5R,6S)-3,7-dioxo-6-[1-methyl-1-(4-nitrobenzyloxycarbonyloxy)ethyl]-1-azabicyclo[3.2.0]heptane-2-carboxylate (145.1 mg) and 4-(N,N-dimethylamino)pyridine (3.27 mg) in acetonitrile (7.3 ml) was added dropwise a solution of N,N-diisopropyl-N-ethylamine (56.0 μl) in acetonitrile (0.504 μl), followed by a solution of diphenyl-chlorophosphate (58.3 μl) in acetonitrile (0.525 ml) at 0° C. After stirring for an hour at 0° C., thereto was added a solution of N,N-diisopropyl-N-ethylamine (186.4 μl) in acetonitrile (1.68 ml), followed by 4-mercaptopyridine (31.3 mg) at -15° C. The mixture was allowed to stand overnight at -15° C. The resultant solution was diluted with ethyl acetate (15 ml) and then washed in turn with water and saturated aqueous sodium chloride. After drying over magnesium sulfate, the solution was filtered and evaporated in vacuo. The residue was chromatographed on silica gel (4 g) eluting with a mixture of benzene and acetone (30:1 to 6:1) to give 4-nitrobenzyl(5R,6S)-3-(4-pyridylthio)-6-[1-methyl-1-(4-nitrobenzyloxycarbonyloxy)ethyl]-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate (139.1 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04640915
Source datasetuspto-grants-1987_02
ORD IDord-fd9f3682bbc5487bbca0457adf4f9b00
Source noteuspto-grants-1987_02