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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895068Generated: October 25, 2026

Dimethylformamide → HCID 178451131, compound

https://huagongshe.com/reaction/895068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactantalpha-t-ButoxycarbonylthienylacetamideHCID 21315147—
ReactantHCID 178508097HCID 178508097—
CatalystFormamideHCID 713—
SolventDiethyl EtherHCID 3283—
ProductHCID 178451131HCID 178451131—

Reaction Steps

7-Amino-3-(1-carboxymethyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid (1.0 g., 2.68 mmol.) was suspended in 10 ml. of dry dimethylformamide and 1.12 ml. of triethylamine was added followed by 85 drops of formamide. A solution of 0.91 g. (2.68 mmol.) of the activated ester of α-t-butoxycarbonylthienylacetamide, prepared as described above, in 2 ml. of dimethylformamide was added and the reaction mixture was stirred at 25° for three hours. An additional 0.45 g. of activated ester was then added and the mixture stirred another five hours. Ether (ca. 300 ml.) was added and the solution was decanted. The remaining oily material was washed with ether, dissolved in water and the aqueous solution was extracted with ethyl acetate. The pH of the ethyl acetate solution was adjusted to 1.5 by addition of dilute hydrochloric acid. Extraction with ethyl acetate and evaporation of the solvent gave 7-(α-t-butoxycarbonylthienylacetamido)-3-(1-carboxymethyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04286089
Source datasetuspto-grants-1981_08
ORD IDord-3c0bb7e1f7bf4e45b896cdd0ceaf9a1b
Source noteuspto-grants-1981_08