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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346392Generated: October 30, 2026

Trifluoroacetate → HCID 131717055, compound

https://huagongshe.com/reaction/346392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetateHCID 84468—
ReactantSodium BicarbonateHCID 516892—
Reactant35831-80-2HCID 6992107—
ReactantHCID 131717057HCID 131717057—
ReactantHCID 178515918HCID 178515918—
SolventWaterHCID 962—
ProductHCID 131717055HCID 13171705516.6%

Reaction Steps

The trifluoroacetate obtained by the same operation as in EXAMPLE 26 by using 800 mg (0.86 mmol) of benzhydryl 3-iodomethyl-7β-[2-ethoxyimino-2-(2-tritylaminothiazol-4-yl) acetamido]-3-cephem-4-carboxylate (syn-isomer) and 300 mg (1.33 mmol) of 2-mercapto-5-(3,4-dihydroxyphenyl)-1,3, 4-thiadiazole, was suspended in water and adjusted to pH6.5 with a saturated sodium hydrogencarbonate. The suspension was subjected to ODS column chromatography (LC Sorb RP-18, manufactured by Kemco Co.) and eluted with a 40% methanol aqueous solution. The fraction containing the desired compound was concentrated and freeze-dried to obtain 106 mg (yield: 16.6%) of the above identified compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05061794
Source datasetuspto-grants-1991_10
ORD IDord-7b3ef6f6229646bb98d104d832a21c49
Source noteuspto-grants-1991_10