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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

反応式

関与物質

役割名称HCID仕込み量
反応物Nicotinic AcidHCID 938—
反応物AmlodipineHCID 2162—
溶媒EthanolHCID 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-carboxylateHCID 8659039085%

反応条件

温度0 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06699892B2
出典データセットuspto-grants-2004_03
ORD IDord-08d6d8aa25df402e84fb3648a2237202
出典メモuspto-grants-2004_03