化工社化工社 化学情報印刷レポート · 研究参考用
s-Glycerylcysteine → N-Fluorenylmethoxycarbonyl-S-(2,3-dihydroxypropyl)cysteine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | s-Glycerylcysteine | HCID 15060047 | — |
| 反応物 | fluorenylmethoxycarbonyl-N-hydroxysuccinimide | HCID 21219419 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 溶媒 | Sodium Carbonate | HCID 10340 | — |
| 生成物 | N-Fluorenylmethoxycarbonyl-S-(2,3-dihydroxypropyl)cysteine | HCID 66831030 | 63.8% |
反応手順
S-(2,3-dihydroxypropyl)cysteine (2.45 g, 12.6 mmole) was dissolved in 9% sodium carbonate (20 ml). A solution of fluorenylmethoxycarbonyl-N-hydroxysuccinimide (3.45 g, 10.5 mmole) in acetonitrile (20 ml) was added and the mixture stirred for 2 h, then diluted with water (240 ml), and extracted with diethyl ether (25 ml×3). The aqueous phase was acidified to pH 2 with concentrated hydrochloric acid and was then extracted with ethyl acetate (70 ml×3). The extract was washed with water (50 ml×2) and saturated sodium chloride solution (50 ml×2), dried over sodium sulfate and evaporated to dryness. Recrystallisation from ether and ethyl acetate at −20° C. yielded a colourless powder (2.8 g, 6.7 mmole, 63.8%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08986700B2 |
| 出典データセット | uspto-grants-2015_03 |
| ORD ID | ord-28dfebcd65ac47ea9e23ecc51f6db15d |
| 出典メモ | uspto-grants-2015_03 |