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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904646Generated: October 31, 2026

4-Methylthiazole-5-carboxaldehyde → HCID 131715960, compound

https://huagongshe.com/reaction/1904646

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methylthiazole-5-carboxaldehydeHCID 581339—
ReactantHCID 13728347HCID 13728347—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductHCID 131715960HCID 13171596059.4%

Reaction Steps

Benzhydryl 7-(phenoxyacetamido)-3-(triphenylphosphoran-diylmethyl)-3-cephem-4-carboxylate (1.55 g ) and 4-methylthiazol-5-carboaldehyde (0.305 g) were dissolved in methylene chloride (20 ml), to which aqueous saturated sodium bicarbonate (20 ml) was added at ambient temperature. The resultant mixture was stirred for 17 hours at ambient temperature. The mixture was allowed to stand until it separated into the aqueous phase and organic solvent phase. The aqueous phase was removed and washed with methylene chloride (20 ml), and the washings (in methylene chloride) were combined with the organic solvent phase separated. The combined solution was dried over anhydrous magnesium sulfate and then concentrated to dryness under reduced pressure. The solid residue obtained was purified chromatographically on a column of silica gel (Wako gel C-300) (40 g) as developed with benzene-ethyl acetate (5:1) as the development solvent. The entitled compound, 7-(phenoxyacetamido)-3-[2-(4-methylthiazol-5-yl)vinyl]-3-cephem-4-carboxylic acid benzhydryl ester (0.741 g) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04839350
Source datasetuspto-grants-1989_06
ORD IDord-16297abe600c43329e6363dcb7550ef5
Source noteuspto-grants-1989_06