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HRID 323536作成日:2026年10月24日

Penicillin G → (S)-ethyl-3-(phenoxyacetamido)-5-(trimethylsilyl)-4-pentynoate

https://huagongshe.com/ja/reaction/323536

反応式

関与物質

役割名称HCID仕込み量
反応物Penicillin GHCID 5904—
反応物Sodium HydroxideHCID 14798—
反応物HCID 20644236HCID 20644236—
溶媒PhosphateHCID 1061—
生成物(S)-ethyl-3-(phenoxyacetamido)-5-(trimethylsilyl)-4-pentynoateHCID 54332815—

反応手順

Racemic ethyl 3-(phenoxyacetamido)-5-(trimethylsilyl)-4-pentynoate (1g) was suspended in phosphate buffer (250 mL, 0.01 molar, prepared from 0.1 molar pH 7.24 solution obtained from sigma). The pH of the solution was adjusted 7.8 using dilute sodium hydroxide. Under slow stirring, 100 units of immobilized penicillin G acylase (Boehringer-Mannheim) was added. The reaction mixture was stirred at room temperature for 48 hours. The reaction mixture was extracted with ethyl acetate (75 mL×3). The organic extracts were combined, dried over sodium sulfate, filtered and evaporated to dryness to give the desired amide, (S)-ethyl-3-(phenoxyacetamido)-5-(trimethylsilyl)-4-pentynoate. The immobilized enzyme was filtered off from the aqueous phase using Whatman No.1 filter paper. The pH of the aqueous phase was adjusted to 8.0 using dilute sodium hydroxide, and extracted with ethyl acetate (75 mL×3). The extracts were combined, dried over sodium sulfate, filtered and evaporated to dryness to give the desired amine, (R)-ethyl-3-amino-5-(trimethylsilyl)-4-pentynoate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06214609B1
出典データセットuspto-grants-2001_04
ORD IDord-a134e06962504c938f001d697517685b
出典メモuspto-grants-2001_04