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HRID 27067作成日:2026年10月26日

3-Nitrobenzaldehyde → 3-(1-Benzylpyrrolidin-3-yl) 5-methyl 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate

https://huagongshe.com/reaction/27067

反応式

関与物質

役割名称HCID仕込み量
反応物3-NitrobenzaldehydeHCID 7449—
反応物Methyl 3-aminocrotonateHCID 643918—
反応物1-Benzyl-3-acetoacetoxypyrrolidineHCID 13652812—
溶媒IsopropanolHCID 3776—
溶媒ChloroformHCID 6212—
生成物3-(1-Benzylpyrrolidin-3-yl) 5-methyl 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylateHCID 229669.2%

反応手順

In 5 ml of isopropyl alcohol were dissolved 1.5 g (0.01 mole) of 3-nitrobenzaldehyde, 2.6 g (0.01 mole) of 1-benzyl-3-acetoacetyloxypyrrolidine, and 1.3 g (0.01 mole) of β-aminocrotonic acid methyl ester and then the solution was refluxed for 8 hours. The solvent was distilled off under reduced pressure, the residue obtained was dissolved in a small amount of chloroform, and the solution was applied to silica gel column chromatography (column diameter 1.5 cm, height 20 cm, and about 200 ml of chloroform was used as the eluant). The eluates were collected and concentrated to give 3.4 g of oily 2,6-dimethyl-4-(3'-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid-3-(1-benzylpyrrolidin-3-yl)ester-5-methyl ester.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04220649
出典データセットuspto-grants-1980_09
ORD IDord-937b1a4b3c184e5f9777790382258d4d
出典メモuspto-grants-1980_09