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Ammonium Hydroxide → 3-Hydroxy-1-adamantyl-D-glycine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonium Hydroxide | HCID 14923 | — |
| 反応物 | Ammonium formate | HCID 2723923 | — |
| 反応物 | 2-(3-Hydroxy-1-adamantyl)-2-oxoacetic acid | HCID 10466193 | — |
| 触媒 | D-1,4-Dithiothreitol | HCID 446094 | — |
| 生成物 | 3-Hydroxy-1-adamantyl-D-glycine | HCID 10263078 | 105.5% |
反応手順
A 266 ml solution was prepared containing ammonium formate (16.74 g, 0.2654 moles) and (3-hydroxy-adamantan-1-yl)-oxo-acetic acid (29.76 g, 0.1327 moles) and brought to pH 8.0 with 12.7 ml concentrated ammonium hydroxide. AND (372 mg, 0.561 mmoles) and dithiothreitol (81.8 mg, 0.530 mmoles) were added, then the solution was added to the bottle containing the Escherichia coli extract. The bottle was maintained at 400 on a shaker at 40 rpm. Concentrated ammonium hydroxide was added periodically to maintain pH 8.0 After 38 hours, the solution contained 31.5 grams (0.140 moles, 100% yield) (S)-amino-(3-hydroxy-adamantan-1-yl)-acetic acid as measured by HPLC analysis and no R-enantiomer of the amino acid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07420079B2 |
| 出典データセット | uspto-grants-2008_09 |
| ORD ID | ord-fba9cc6497f849189f6520cea1fab0f0 |
| 出典メモ | uspto-grants-2008_09 |