戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 256601作成日:2026年10月26日

Isopropanol → Nilvadipine

https://huagongshe.com/reaction/256601

反応式

関与物質

役割名称HCID仕込み量
反応物IsopropanolHCID 3776—
反応物Sodium CarbonateHCID 10340—
反応物Phosphorus pentachlorideHCID 24819—
反応物6-Cyano-5-methoxycarbonyl-2-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylic acidHCID 15388766—
溶媒DichloromethaneHCID 6344—
生成物NilvadipineHCID 449495.4%

反応手順

In methylene chloride (30 ml) is suspended methyl (+)-5-carboxy-2-cyano-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate (3.12 g) followed by addition of phosphorus pentachloride (2.46 g) with ice-cooling, and the mixture is stirred for 30 minutes. Then, a solution of isopropyl alcohol (1.4 g) in methylene chloride (10 ml) is added dropwise over a period of 10 minutes. The mixture is stirred for 20 minutes, at the end of which time 5% aqueous sodium carbonate solution (30 ml) is added and the mixture is stirred at ambient temperature for one hour. The organic layer is separated and the water layer is extracted with methylene chloride. The organic layers are combined, washed with aqueous sodium chloride solution, dried over anhydrous magnesium sulfate and distilled under reduced pressure to remove the solvent. The residue is purified by silica gel (75 g) column chromatography, elution being carried out with benzeneethyl acetate (10:1). The solvent is removed from the eluate under reduced pressure and the residue is crystallized from diisopropyl ether to provide 5-isopropyl 3-methyl (+)-2-cyano-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate (3.34 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05258393
出典データセットuspto-grants-1993_11
ORD IDord-77bfd4d9bb8e4b79a65d1edd92bfbd1b
出典メモuspto-grants-1993_11