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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352686Generated: October 31, 2026

Trifluoroacetic acid → HCID 131711752, compound

https://huagongshe.com/reaction/2352686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 131712300HCID 131712300—
SolventDiethyl EtherHCID 3283—
ProductHCID 131711752HCID 13171175231.1%

Reaction Steps

Trifluoroacetic acid (3 ml) was added under ice-cooling to 7-[2-methoxyimino-2-(2-t-pentyloxycarbonylamino-1,3-thiazol-4-yl)acetamido]-3-(5-methyl-1,3,4-thiadiazol-2-yl)thiomethyl-3-cephem-4-carboxylic acid (syn isomer) (0.5 g) and the mixture was stirred for 30 minutes at ambient temperature. To the mixture was added ether and precipitating powder was collected by filtration and dissolved in a mixture of water (20 ml) and an 1N aqueous solution of sodium hydroxide to adjust to pH 12 to 13. The solution was adjusted to pH 4.6 with 10% hydrochloric acid, washed with ethyl acetate and methylene chloride. Excess methylene chloride in the aqueous layer was throughly removed by bubbling of nitrogen gas. The aqueous layer was adjusted to pH 2 with stirring and ice-cooling to precipitate powder. The powder was collected by filtration and dried to give 7-[2-methoxyimino-2-(2-amino-1,3-thiazol-4-yl)acetamido]-3-(5-methyl-1,3,4-thiadiazol-2-yl)thiomethyl-3-cephem-4-carboxylic acid (syn isomer) (0.128 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04877873
Source datasetuspto-grants-1989_10
ORD IDord-daade28a2ec04ff8b505a8347856640c
Source noteuspto-grants-1989_10