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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258685Generated: October 30, 2026

Triethylamine → HCID 70620430, compound

https://huagongshe.com/reaction/258685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-(2,2,2-Trifluoroethanesulfinyl)acetic acidHCID 20574023—
Reactant7-Amino-3-(5-carboxymethyl-1,3,4-oxadiazol-2-ylthiomethyl)-3-cephem-4-carboxylic acidHCID 70620465—
SolventDimethylformamideHCID 6228—
ProductHCID 70620430HCID 70620430—

Reaction Steps

A suspension of 3.4 g (0.01 mol) of 7-amino-3-(5-carboxymethyl-1,3,4-oxadiazol-2-ylthiomethyl)-3-cephem-4-carboxylic acid in 50 ml of dry dimethylformamide is treated with 2 of triethylamine and the mixture is stirred for 15 minutes at 25°. A slight excess of 0.01 mol of the activated ester of 2,2,2-trifluoroethylsulfinylacetic acid is added to the mixture and it is stirred an additional hour. The reaction mixture is evaporated to dryness in vacuo and water and ethyl acetate are added to the residue. The layers are separated, the ethyl acetate layer is discarded, fresh ethyl acetate is added to the aqueous phase and it is acidified to pH 2.5 by addition of 6N hydrochloric acid. The mixture is filtered, the layers are separated and the aqueous phase is extracted with ethyl acetate. The combined extracts are washed with water, dried (MgSO4) and evaporated to dryness to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04034092
Source datasetuspto-grants-1977_07
ORD IDord-c40a0088d95349eb85947db0bbf7075e
Source noteuspto-grants-1977_07