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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903032Generated: November 1, 2026

Pyridine → 7-Phenoxyacetamido-3-methyl-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/1903032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
ReactantThionyl ChlorideHCID 24386—
Reactant7-(2-Phenoxyacetamido)-3-methyl-3-bromocepham-4-carboxylic acidHCID 70361010—
Solvent1,1-DichloroethaneHCID 6365—
Product7-Phenoxyacetamido-3-methyl-3-cephem-4-carboxylic acidHCID 1557340011.5%

Reaction Steps

A solution of 7-(2-phenoxyacetamido)-3-methyl-3-bromocepham-4-carboxylic acid (860 mg.) in dry dichloroethane (20 cc) was cooled at -40°--50° C. and pyridine and a 10% dichloromethane solution (4.7 g.) of thionyl chloride were respectively added thereto. The mixture was stirred at -40°--50° C. for one hour and then at room temperature overnight, and poured into ice water and stirred for 30 minutes. The dichloroethane layer was extracted with an aqueous sodium bicarbonate solution and the aqueous layer was acidified with phosphoric acid and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried, treated with carbon powder and then concentrated to yield crystals (80 mg.) of 7-(2-phenoxyacetamido)-3-methyl-3-cephem-4-carboxylic acid, m.p. 172°-175° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04435321
Source datasetuspto-grants-1984_03
ORD IDord-65ca0e52f6574d72a882bccdfa8fd9e9
Source noteuspto-grants-1984_03