関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Penicillin G | HCID 5904 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | HCID 20644236 | HCID 20644236 | — |
| 溶媒 | Phosphate | HCID 1061 | — |
| 生成物 | (S)-ethyl-3-(phenoxyacetamido)-5-(trimethylsilyl)-4-pentynoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06214609B1 |
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| 出典データセット | uspto-grants-2001_04 |
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| ORD ID | ord-a134e06962504c938f001d697517685b |
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| 出典メモ | uspto-grants-2001_04 |
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