HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345631Generated: October 25, 2026
Phosphate → (2R,3S)-3-Phenoxyacetylamino-2-[(2-furanyl)ethyl]-4-oxo-1-azetidine acetic acid, methyl ester
https://huagongshe.com/reaction/345631
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphate | HCID 1061 | — |
| Reactant | Penicillin G | HCID 5904 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methyl phenoxyacetate | HCID 16365 | — |
| Reactant | HCID 86745171 | HCID 86745171 | — |
| Solvent | Water | HCID 962 | — |
| Product | (2R,3S)-3-Phenoxyacetylamino-2-[(2-furanyl)ethyl]-4-oxo-1-azetidine acetic acid, methyl ester | HCID 9886466 | 13% |
Reaction Steps
A 100 mg sample of [(2R,3S),(2S,3R)]-3-amino- <2-[2-(2-furanyl)ethyl]-4-oxo-1-azetidine acetic acid, methyl ester oxalate salt and a 135 mg sample of methyl phenoxyacetate were added to 0.lM phosphate buffer (100 ml final volume) and adjusted to pH=6.0 with lN KOH. Milli-Q™ H2O washed Sclavo penicillin G amidase (40 I.U. of enzyme per gram of substrate) was then added to the reaction mixture and the pH of reaction mixture was maintained at 6.0 and temperature at 28° C. for 8 hours. The reaction mixture was then filtered to remove the immobilized enzyme and extracted two times with ethyl acetate. The organic extracts were then dried over anhydrous sodium sulfate and concentrated to dryness in vacuo. The title compound was then isolated by column chromatography from this residue using a Kiesegel 60™ column eluted with toluene/ethyl acetate (70/30). Yield: 13%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05057607 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-678c2905b4724c37ac1f44b76fa1f741 |
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| Source note | uspto-grants-1991_10 |
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