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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1659791Generated: November 3, 2026

HCID 131712609, compound → HCID 131712608, compound

https://huagongshe.com/reaction/1659791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131712609HCID 131712609—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131712608HCID 13171260872.8%

Reaction Steps

Platinic oxide (0.4 g.) was added to a solution of benzhydryl 7-[2-methoxyimino-2-(2-aminothiazol-4-yl)acetamido]-3-(4-nitrobenzoyloxymethyl)-3-cephem-4-carboxylate (syn isomer) (4.3 g.) in a mixture of ethanol (50 ml.) and tetrahydrofuran (50 ml.), and the suspension was subjected to catalytic reduction at ambient temperature under ordinary pressure for 3 hours. After removing the catalyst from the resultant mixture by filtration, the filtrate was evaporated under reduced pressure. The residue was dissolved in ethyl acetate and the solution was washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate and evaporated in vacuo. The residue was pulverized with diethyl ether to give benzhydryl 7-[2-methoxyimino-2-(2-aminothiazol-4-yl)acetamido]-3-(4-aminobenzoyl-oxymethyl)-3-cephem-4-carboxylate (syn isomer) (3.0 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04304770
Source datasetuspto-grants-1981_12
ORD IDord-64edef6a734148d1bb79c4c907fb2278
Source noteuspto-grants-1981_12