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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609658Generated: October 25, 2026

Diisopropyl Ether → 7beta-formamido-3-[N,N-dimethyl-N-{(5-hydroxy-4-oxo-1,4-dihydropyridin-2-yl) methyl}ammonio]methyl-3-cephem-4-carboxylate

https://huagongshe.com/reaction/1609658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropyl EtherHCID 7914—
ReactantSodium 2-ethylhexanoateHCID 23672331—
Reactant2-(N,N-dimethylamino)methyl-5-hydroxy-4-pyridoneHCID 67748063—
Reactant7beta-Formamido-3-chloromethyl-3-cephem-4carboxylic acidHCID 88300534—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product7beta-formamido-3-[N,N-dimethyl-N-{(5-hydroxy-4-oxo-1,4-dihydropyridin-2-yl) methyl}ammonio]methyl-3-cephem-4-carboxylateHCID 8839985643.2%

Reaction Steps

2-(N, N-Dimethylamino) methyl-5-hydroxy-4-pyridone (15.85 g) was dissolved in N,N-dimethylformamide (238 ml) by addition of sodium 2-ethylhexanoate (10.44 g) . To the resulting solution was added dropwise a cooled solution of 7β-formamido-3-chloromethyl-3-cephem-4carboxylic acid (13.04 g) at 5° C. and the mixture was stirred for 2 hours at the same temperature. The mixture was added dropwise to a mixture of ethyl acetate (2.5 l) and diisopropyl ether (2.5 l) and the resulting precipitates were collected by filtration, washed three times with a mixture of ethyl acetate and diisopropyl ether (1:1) and dried in vacuo. The powder was poured into cold water (300 ml) and the mixture was adjusted to pH 3.0 with 1N hydrochloric acid. After the insoluble materials were filtered off, the filtrate was chromatographed on Diaion HP-20 (1300 ml) at 50° C. and the elution was carried out with 10% aqueous isopropyl alcohol. The eluate was lyophilized to give 7β-formamido-3-[N,N-dimethyl-N-{(5-hydroxy-4-oxo- 1,4-dihydropyridin-2-yl)methyl}ammonio]methyl-3-cephem-4carboxylate (8.31 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05401734
Source datasetuspto-grants-1995_03
ORD IDord-820f35a65ea542b3a857c378fb492a98
Source noteuspto-grants-1995_03