Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Penicillin G | HCID 5904 | — |
| Reactant | Methyl phenylacetate | HCID 7559 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | HCID 19826320 | HCID 19826320 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15670703 | HCID 15670703 | 42.2% |
Reaction Steps
A 100 mg sample of cis(racemic at 2 and 3 position) 3-amino-2-[2-(2-furanyl)ethyl]-4-oxo-1-azetidine acetic acid, methyl ester oxalate and 121 mg of methyl phenylacetate was added to 0.1 M potassium phosphate buffer(100ml) at pH=6.0, and the temperature maintained at 28° C. Milli-Q™ H2O washed Sclavo penicillin G amidase (0.035 I.U./%mole of substrate; 0.100 I.U./mg of substrate) was added and the reaction allowed to proceed overnight. The reaction mixture was then extracted two times with ethyl acetate and dried over anhydrous sodium sulfate. The ethyl acetate portion was evaporated to dryness in vacuo and the residue was purified by column chromatography using a Kiesegel 60™ column eluted with toluene/ethyl acetate (50/50), to obtain 45.7 mg (42.2% yield) of the title compound.
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-685a014d39a442f0bdbb97ca1f420884 |
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| Source note | uspto-grants-1991_10 |
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