HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847196Generated: October 27, 2026
Diphenyl chlorophosphate → p-Nitrobenzyl 2-azidocarbapen-2-em-3-carboxylate
https://huagongshe.com/reaction/847196
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diphenyl chlorophosphate | HCID 75654 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Potassium azide | HCID 10290740 | — |
| Reactant | p-Nitrobenzyl 2-oxo-carbapenam-3-carboxylate | HCID 131715742 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | p-Nitrobenzyl 2-azidocarbapen-2-em-3-carboxylate | HCID 131715741 | 19.2% |
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, filtered, 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05140030 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-33c3112a12e9434595fd710d1931f177 |
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| Source note | uspto-grants-1992_08 |
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