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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906085Generated: November 1, 2026

HCID 131714214, compound → HCID 131714213, compound

https://huagongshe.com/reaction/1906085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131714214HCID 131714214—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131714213HCID 13171421374.9%

Reaction Steps

4-Nitrobenzyl 7-[2-t-butoxycarbonylmethoxyimino-2-(4-thiazolyl)acetamido]-3-methoxy-3-cephem-4-carboxylate (syn isomer) (2.9 g) was dissolved in a mixed solution of methanol (50 ml), tetrahydrofuran (30 ml) and glacial acetic acid (0.5 ml). After adding 10% palladium on carbon (1.5 g) to the solution, the mixture was subjected to catalytic reduction at ambient temperature under atmospheric pressure. The catalyst was filtered off and the filtrate was concentrated under reduced pressure. Water and ethyl acetate were added to the residue and the mixture was adjusted to pH 7.5 with a saturated aqueous solution of potassium carbonate. The separated aqueous layer was adjusted to pH 2.0 with 10% hydrochloric acid and extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate and evaporated to give 7-[2-t-butoxycarbonylmethoxyimino-2-(4-thiazolyl)acetamido]-3-methoxy-3-cephem-4-carboxylic acid (syn isomer) (1.71 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04649136
Source datasetuspto-grants-1987_03
ORD IDord-674f0687a8c04882b3f94deb16a2d56b
Source noteuspto-grants-1987_03