関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | Galantamine Hydrobromide | HCID 121587 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | (-)-Galantamine | HCID 9651 | — |
反応手順
The resulting 88% galanthamine hydrobromide is suspended in 7.6 l of water. The suspension is cooled to 0° C. and diluted, keeping the temperature from 0 to 5° C., with 5.2 l of 10% sodium carbonate. Five extractions with 5 l of n-butyl acetate are obtained, the organic phases are pooled and washed with 2.5 l of salted water. The organic phases are concentrated under vacuum to a volume of 4 l and allowed to crystallize at room temperature. The crystals are filtered and dried under vacuum at 70° C. 1.2 kg of galanthamine are obtained with chemical-physical and spectroscopical characteristics consistent with those reported in the literature (P. Carroll et al., Bull. Soc. Chim. Fr. (1990), 127, 769).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08013151B2 |
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| 出典データセット | uspto-grants-2011_09 |
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| ORD ID | ord-433912ffc71b4efe8a37e31941b00aba |
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| 出典メモ | uspto-grants-2011_09 |
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