戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 22461作成日:2026年10月26日

Galantamin → (+)-Narwedine

https://huagongshe.com/reaction/22461

反応式

関与物質

役割名称HCID仕込み量
反応物GalantaminHCID 3449—
反応物(-)-GalantamineHCID 9651—
反応物Galantamine, (+)-HCID 906210—
反応物NarwedineHCID 10356588—
生成物(+)-NarwedineHCID 441596—

反応手順

Once dissolved, the racemic narwedine mixture is maintained at a temperature of 25° C. to 70° C., preferably 40° C. to 60° C., and the crystals of enantiomeric narwedine, enantiomeric galanthamine, or enantiomeric epigalanthamine in an amount of from 0.1% to 2%, preferably 0.2% to 1% by weight relative to the amount of narwedine to be resolved are added. If (-)-narwedine is to be produced, the crystals added here are either (-)-narwedine, (+)-galanthamine, or (+)-epigalanthamine. If the reaction is to produce (+)-narwedine, the crystal used here are (+)-narwedine, (-)-galanthamine or (-)-epigalanthamine. Since the end result of the next step (the reduction to (-)-galanthamine) is intended to be as free as possible of epigalanthamine and (+)-galanthamine, (-)-narwedine is the most preferred crystal to use to generate additional (-)-narwedine so long as it is available. The temperature is then dropped to 25° to 70° C., preferably 40° C. to 60° C. and held there for 5-24 hours, preferably 12-18 hours, most preferably about 16 hours.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05428159
出典データセットuspto-grants-1995_06
ORD IDord-f6205e02a6c94ac6bce8060a9027a0b6
出典メモuspto-grants-1995_06