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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylthiazole-5-carboxaldehyde | HCID 581339 | — |
| Reactant | HCID 13728347 | HCID 13728347 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 131715960 | HCID 131715960 | 59.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04839350 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-16297abe600c43329e6363dcb7550ef5 |
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| Source note | uspto-grants-1989_06 |
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