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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248879Generated: October 30, 2026

Triethylamine → HCID 131714984, compound

https://huagongshe.com/reaction/1248879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 70468832HCID 70468832—
ReactantHCID 178482017HCID 178482017—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductHCID 131714984HCID 13171498471%

Reaction Steps

1.0 g. of 7-bromoacetamido-3-acetylaminomethylceph-3-em-4-carboxylic acid, 0.3 g. of 1-methyl-5-mercapto-1H-tetrazole and 9.1 g. of triethyl amine were dissolved in 20 ml. of anhydrous dimethyl formamide. The reaction mixture was stirred at room temperature for 12 hours. First 0.7 g. of calcinated potassium carbonate, then 30 ml. of ether were added to the reaction mixture. The precipitate separated was filtered off, dissolved in water, the pH of the solution was adjusted to 2 by adding diluted sulphuric acid and the mixture was extracted with ethyl acetate. The organic extract was dried over anhydrous magnesium sulphate. The solvent was evaporated in vacuo and the residue was treated with diethyl ether. Thus 0.76 g. of 7-(1-methyl-1H-tetrazole-5-ylthio)-acetamido-3-acetylaminomethylceph-3-em-4-carboxylic acid were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04626533
Source datasetuspto-grants-1986_12
ORD IDord-5b988c5bee5542cbb9527c5a6698e2e9
Source noteuspto-grants-1986_12