Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164428Generated: November 1, 2026

Pyridine → HCID 88683653, compound

https://huagongshe.com/reaction/1164428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenoxyacetyl chlorideHCID 69703—
ReactantHCID 88684178HCID 88684178—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 88683653HCID 88683653117.4%

Reaction Conditions

Temperature-25 °C

Reaction Steps

In methylene chloride (10 ml) are dissolved 2,2,2-trichloroethyl 7β-methoxyamino-3-methyl-3-cephem-4-carboxylate (320 mg) and pyridine (134 mg) and the mixture is cooled to -25° C. To this mixture is added phenoxyacetyl chloride (171 mg), followed by stirring for 20 minutes. The reaction mixture is poured in a mixture of ethyl acetate and water and the organic layer is taken. The organic layer is washed with 1 N-HCl, aqueous sodium hydrogen carbonate and aqeuous sodium chloride in that-order, dried over magnesium sulfate and concentrated. The above procedure gives 2,2,2-trichloroethyl 7-(N-methoxy-2-phenoxyacetamido)-3-methyl-3-cephem-4-carboxylate (510 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04369312
Source datasetuspto-grants-1983_01
ORD IDord-eca04a93041140049f59a0760eb7c869
Source noteuspto-grants-1983_01