戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2219846作成日:2026年10月27日

Acetone → sodium;(E)-7-[3-(4-fluorophenyl)-1-propan-2-ylindol-2-yl]-3,5-dihydroxyhept-6-enoate

https://huagongshe.com/reaction/2219846

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物Sodium HydroxideHCID 14798—
反応物(6E)-7-(3-(4-fluorophenyl)-1-(propan-2-yl)-1H-indol-2-yl)-3,5-dihydroxyhept-6-enoic acidHCID 5353627—
溶媒MethanolHCID 887—
生成物sodium;(E)-7-[3-(4-fluorophenyl)-1-propan-2-ylindol-2-yl]-3,5-dihydroxyhept-6-enoateHCID 1676042562%

反応手順

Fluvastatin (3 g) was completely dissolved in MeOH (15 ml) at reflux temperature. Then, the solution was filtered to obtain a clear solution and heated to reflux again. NaOH (s) (0.29 g) was added at reflux temperature to obtain a precipitate. The slurry was cooled to room temperature to obtain a paste-like mixture. Acetone (30 g) was added dropwise at room temperature and the solution stirred at room temperature for 21 h to obtain a massive precipitate. The product was filtered under nitrogen flow, washed with acetone (2×15 ml) and dried at 50° C. in a vacuum oven for 22.5 h to obtain 1.89 g (62%) of fluvastatin sodium Form XLVIII.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07414140B2
出典データセットuspto-grants-2008_08
ORD IDord-f2341bb8e61d4ca48c6469e1f07324c7
出典メモuspto-grants-2008_08