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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34497Generated: October 30, 2026

Trifluoroacetic acid → HCID 178481649, compound

https://huagongshe.com/reaction/34497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAnisoleHCID 7519—
ReactantDiisopropyl EtherHCID 7914—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178481648HCID 178481648—
SolventDichloromethaneHCID 6344—
ProductHCID 178481649HCID 17848164984.6%

Reaction Steps

To a mixture of benzhydryl 7-[2-(2-tritylaminothiazol-4-yl)-2-difluoromethoxyiminoacetamido]-3-(4-methyl-5-oxo-6-hydroxy-4,5-dihydro-1,2,4-triazin-3-yl)thiomethyl-3-cephem-4-carboxylate (syn isomer) (1.20 g) and anisole (2.5 ml) in methylene chloride (2.5 ml) was added trifluoroacetic acid (5 ml) under ice-cooling. After being stirred for 30 minutes, the mixture was poured into diisopropyl ether (50 ml). The resultant mixture was adjusted to pH 7 with an aqueous solution of sodium bicarbonate. The separated aqueous layer was washed with ethyl acetate, acidified with 6N hydrochloric acid and extracted with a mixture of tetrahydrofuran and ethyl acetate. The extract was washed with a saturated aqueous solution of sodium chloride, dried and evaporated under reduced pressure. The residue was triturated in diethyl ether and collected by filtration to give 7-[2-(2-aminothiazol-4-yl)-2-difluoromethoxyiminoacetamido]-3-(4-methyl-5-oxo-6-hydroxy-4,5-dihydro-1,2,4-triazin-3-yl)thiomethyl-3-cephem-4-carboxylic acid (syn isomer) (600 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04761410
Source datasetuspto-grants-1988_08
ORD IDord-1b11f740150d4069855dec58ac63b00e
Source noteuspto-grants-1988_08