HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992679Generated: October 31, 2026
Diisopropylethylamine → Diphenylmethyl 7beta-formamido-3-[(4-pyridyl)methylthio]-3-cephem-4-carboxylate
https://huagongshe.com/reaction/992679
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Diphenylmethyl 7beta-formamido-3-methanesulfonyloxy-3-cephem-4-carboxylate | HCID 10863874 | — |
| Reactant | Pyridin-4-ylmethanethiol | HCID 13092602 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Diphenylmethyl 7beta-formamido-3-[(4-pyridyl)methylthio]-3-cephem-4-carboxylate | HCID 88157711 | 88.4% |
Reaction Steps
To a solution of diphenylmethyl 7β-formamido-3-methanesulfonyloxy-3-cephem-4-carboxylate (14.66 g, 30 m mol) in DMF (103 ml) was added 4-(mercaptomethyl)pyridine (4.13 g, 33 m mol) at −20° C., followed by dropwise addition of N,N-diisopropylethylamine (3.88 g, 30 m mol). The mixture was stirred at the same temperature for 1.9 hours and poured into ice water (500 ml). The resulting precipitates were collected by filtration and washed with water. The powder was dissolved in THF, and ethyl acetate and water were added respective. The separated organic layer was washed with brine, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by column chromatography on silica gel to give diphenylmethyl 7β-formamido-3-[(4-pyridyl)methylthio]-3-cephem-4-carboxylate (13.73 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06468995B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-cceead8440d241e1be5be0bda81c26b1 |
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| Source note | uspto-grants-2002_10 |
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