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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329665Generated: October 27, 2026

18-Crown-6 → p-Nitrobenzyl 2-azidocarbapen-2-em-3-carboxylate

https://huagongshe.com/reaction/329665

Reaction equation

Participants

RoleNameHCIDCharge
Reactant18-Crown-6HCID 28557—
ReactantDiphenyl chlorophosphateHCID 75654—
ReactantDiisopropylethylamineHCID 81531—
ReactantPotassium azideHCID 10290740—
Reactantp-Nitrobenzyl 2-oxo-carbapenam-3-carboxylateHCID 131715742—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetonitrileHCID 6342—
Productp-Nitrobenzyl 2-azidocarbapen-2-em-3-carboxylateHCID 13171574119.2%

Reaction Steps

Diphenyl chlorophosphate (10.9 microliter, 52.6 micromol) was added to a stirred, 0° C. solution of a p-nitrobenzyl 2-oxo-carbapenam-3-carboxylate (15.4 mg, 50.6 micromol), 4-dimethylaminopyridine (1.3 mg, 11 micromol), and diisopropylethylamine (10.4 microliter, 59.7 micromol) in anhydrous acetonitrile (500 microliter). After 5 min., potassium azide (12.6 mg, 155 micromol), and 1,4,7,10,13,16-hexaoxacyclooctadecane (13.3 mg, 50.3 micromol) were added. After an additional 5 min. the mixture was washed three times with water, dried over anhydrous magnesium sulfate, filterd, and evaporated under vacuum. The residue was applied to one 20 cm×20 cm 250 micron silica gel preparative thin layer chromatography plate and developed with diethyl ether. Elution with ethyl acetate and evaporation of the eluate under vacuum provided 3.2 mg (19%) p-nitrobenzyl 2-azido-carbapen-2-em-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04892869
Source datasetuspto-grants-1990_01
ORD IDord-40142fbf38f8426c9bc0c996d916ecf8
Source noteuspto-grants-1990_01