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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphateHCID 1061—
ReactantPenicillin GHCID 5904—
ReactantPotassium HydroxideHCID 14797—
ReactantMethyl phenoxyacetateHCID 16365—
ReactantHCID 86745171HCID 86745171—
SolventWaterHCID 962—
Product(2R,3S)-3-Phenoxyacetylamino-2-[(2-furanyl)ethyl]-4-oxo-1-azetidine acetic acid, methyl esterHCID 988646613%

Reaction Conditions

Temperature28 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05057607
Source datasetuspto-grants-1991_10
ORD IDord-678c2905b4724c37ac1f44b76fa1f741
Source noteuspto-grants-1991_10