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HRID 47598作成日:2026年10月24日
Nicotinic Acid → 3-O-ethyl 5-O-methyl 2-(2-aminoethoxymethyl)-4-(2-chlorophenyl)-6-methyl-1,4-dihydropyridine-3,5-dicarboxylate;pyridine-3-carboxylate
https://huagongshe.com/ja/reaction/47598
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Nicotinic Acid | HCID 938 | — |
| 反応物 | Amlodipine | HCID 2162 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 3-O-ethyl 5-O-methyl 2-(2-aminoethoxymethyl)-4-(2-chlorophenyl)-6-methyl-1,4-dihydropyridine-3,5-dicarboxylate;pyridine-3-carboxylate | HCID 86590390 | 85% |
反応手順
Amlodipine free base (4.09 g) was added to 40 mL of ethanol. The mixture was heated at reflux and stirred until the solid was completely dissolved. Nicotinic acid (1.23 g) was added to the amlodipine solution and then the mixture was slowly cooled down to 0° C. within one hour. The solids formed were isolated by filtration, washed with ethyl acetate and dried under reduced pressure to yield 4.51 g of amlodipine nicotinate.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06699892B2 |
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| 出典データセット | uspto-grants-2004_03 |
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| ORD ID | ord-08d6d8aa25df402e84fb3648a2237202 |
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| 出典メモ | uspto-grants-2004_03 |
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