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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834830Generated: November 1, 2026

Pyridine → HCID 131711023, compound

https://huagongshe.com/reaction/1834830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantChloroformHCID 6212—
ReactantHCID 88606570HCID 88606570—
ProductHCID 131711023HCID 131711023—

Reaction Steps

A mixture of 2,2,2-trichloroethyl 6-[N-(2,2,2-trichloroethoxycarbonyl)phenylglycyl]amino-2-methyl-2-bromomethylpenam-3-carboxylate (0.43 g.), dry pyridine (0.09 g.) and dry chloroform (10 cc) was heated under reflux for 4.5 hours. The chloroform layer was separated, washed with water, dried and then concentrated. The residue was recrystallized from ether to yield needles (0.23 g.) of 2,2,2-trichloroethyl 7-[N-(2,2,2-trichloroethoxycarbonyl)phenylglycyl]amino-3-methyl-3-cephem-4-carboxylate, m.p. 99°-100.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04071527
Source datasetuspto-grants-1978_01
ORD IDord-c4374a11706548509ddccc22f1f7a502
Source noteuspto-grants-1978_01