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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345630Generated: October 31, 2026

Penicillin G → HCID 15670703, compound

https://huagongshe.com/reaction/345630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPenicillin GHCID 5904—
ReactantMethyl phenylacetateHCID 7559—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantHCID 19826320HCID 19826320—
SolventWaterHCID 962—
ProductHCID 15670703HCID 1567070342.2%

Reaction Conditions

Temperature28 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05057607
Source datasetuspto-grants-1991_10
ORD IDord-685a014d39a442f0bdbb97ca1f420884
Source noteuspto-grants-1991_10