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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 345631생성일: 2026년 10월 26일

Phosphate → (2R,3S)-3-Phenoxyacetylamino-2-[(2-furanyl)ethyl]-4-oxo-1-azetidine acetic acid, methyl ester

https://huagongshe.com/reaction/345631

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참여 물질

역할이름HCID투입량
반응물PhosphateHCID 1061—
반응물Penicillin GHCID 5904—
반응물Potassium HydroxideHCID 14797—
반응물Methyl phenoxyacetateHCID 16365—
반응물2-[2-(2-Furanyl)ethyl]-4-oxo-1-azetidine acetic acid, methyl ester oxalate saltHCID 86745171—
용매WaterHCID 962—
생성물(2R,3S)-3-Phenoxyacetylamino-2-[(2-furanyl)ethyl]-4-oxo-1-azetidine acetic acid, methyl esterHCID 988646613%

반응 조건

온도28 °C

반응 단계

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%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05057607
출처 데이터셋uspto-grants-1991_10
ORD IDord-678c2905b4724c37ac1f44b76fa1f741
출처 메모uspto-grants-1991_10