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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858523Generated: November 2, 2026

Trifluoroacetic acid → HCID 178433978, compound

https://huagongshe.com/reaction/1858523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantDiisopropyl EtherHCID 7914—
ReactantHCID 178433977HCID 178433977—
SolventDichloromethaneHCID 6344—
ProductHCID 178433978HCID 17843397874.7%

Reaction Steps

To a solution of 7β-[2-(5-tert-butoxycarbonylamino-1,2,4-thiadiazol-3-yl)acetamido]-3-(5-methyl-1,3,4-thiadiazol-2-yl)thio-3-cephem-4-carboxylic acid (800 mg) in dichloromethane (2.4 ml) was added trifluoroacetic acid (10.4 ml). The mixture was stirred for 30 minutes at room temperature. The reaction mixture was poured into diisopropyl ether (150 ml). The precipitate was collected by filtration and dried. The precipitate was dissolved in a mixture of aqueous sodium hydrogen carbonate (212 mg/30 ml) and tetrahydrofuran (10 ml). The solution was washed with ethyl acetate (30 ml). To the aqueous layer was added a mixture of tetrahydrofuran (15 ml) and ethyl acetate (45 ml), adjusted to pH 2 with 1N-hydrochloric acid. The organic layer was washed with saturated aqueous sodium chloride, dried over magnesium sulfate and concentrated in vacuo. The residue was triturated with diethyl ether to give 7β-[2-(5-amino-1,2,4-thiadiazol-3-yl)acetamido]-3-(5-methyl-1,3,4-thiadiazol-2-yl)thio-3-cephem-4-carboxylic acid (490 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150351
Source datasetuspto-grants-2000_11
ORD IDord-977b584a18734be5981ee9bcc8ae038a
Source noteuspto-grants-2000_11