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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730706Generated: October 26, 2026

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

https://huagongshe.com/reaction/1730706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantEthyl AcetateHCID 8857—
Reactant2-Bromomethyl-2-methyl-6-(2-phenoxyacetamido)penam-3-carboxylic acidHCID 12895258—
SolventBenzeneHCID 241—
Product7-Phenoxyacetamido-3-methyl-3-cephem-4-carboxylic acidHCID 1557340071.8%

Reaction Steps

6-(2-phenoxyacetamido)-2-methyl-2-bromomethylpenam-3-carboxylic acid (429 mg.) was suspended in dry benzene (10 cc), and pyridine (400 mg.) and trimethylsilylchloride (5 cc) were added thereto. The mixture was stirred for 1.5 hours at room temperature and pyridine (400 mg.) was added thereto. The mixture was heated under reflux for 3 hours, mixed with ethyl acetate (30 cc), washed with dilute phosphoric acid and further with an aqueous solution saturated with sodium chloride, dried and then concentrated. A small amount of ethyl acetate was added to the residue and the precipitate was collected by filtration to yield crystals (250 mg.) of 7-(2-phenoxyacetamido)-3-methyl-3-cephem-4-carboxylic acid, m.p. 170.5° - 172° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03993646
Source datasetuspto-grants-1976_11
ORD IDord-62db17ec99264e02a0c05500f94c7238
Source noteuspto-grants-1976_11