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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128210Generated: October 26, 2026

Hydrochloric Acid → Pivaloyloxymethyl 7-[(4-(3-aminopropyl)-1-piperidyl)-methyleneamino]-3-methyl-3-cephem-4-carboxylate, dihydrochloride

https://huagongshe.com/reaction/128210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantPivaloyloxymethyl 7-[(4-(3-azidopropyl)-1-piperidyl)-methyleneamino]-3-methyl-3-cephem-4-carboxylateHCID 131712136—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductPivaloyloxymethyl 7-[(4-(3-aminopropyl)-1-piperidyl)-methyleneamino]-3-methyl-3-cephem-4-carboxylate, dihydrochlorideHCID 131712137—

Reaction Steps

To a stirred solution of pivaloyloxymethyl 7-[(4-(3-azidopropyl)-1-piperidyl)-methyleneamino]-3-methyl-3-cephem-4-carboxylate (1.5 g) in ethyl acetate (25 ml) were added water (30 ml) and hydrochloric acid to pH=3. 10% palladium-on-carbon (0.5 g) was added, and hydrogen was bubbled through the stirred mixture, a pH-value of 3 being maintained by addition of 0.2 N hydrochloric acid. When the consumption of acid ceased, the catalyst was filtered off. The aqueous phase was separated and freeze-dried to yield the desired compound as an amorphous powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04259333
Source datasetuspto-grants-1981_03
ORD IDord-6aaf4f2dad0b4a2ba35360a3f0956e89
Source noteuspto-grants-1981_03