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HRID 25479作成日:2026年10月26日

2-Butenoic acid, 3-amino-, ethyl ester, (2Z)- → 3-Methyl 5-ethyl 4-(2-chlorophenyl)-2-{[2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethoxy]methyl}-6-methyl-1,4-dihydro-3,5-pyridine dicarboxylate

https://huagongshe.com/reaction/25479

反応式

関与物質

役割名称HCID仕込み量
反応物2-Butenoic acid, 3-amino-, ethyl ester, (2Z)-HCID 643756—
反応物Methyl 2-(o-chlorobenzylidene)-4-(2-phthalimidoethoxy)acetoacetateHCID 69267975—
溶媒IsopropanolHCID 3776—
生成物3-Methyl 5-ethyl 4-(2-chlorophenyl)-2-{[2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethoxy]methyl}-6-methyl-1,4-dihydro-3,5-pyridine dicarboxylateHCID 11786009—

反応条件

温度15 °C

反応手順

87 g of methyl 2-(o-chlorobenzylidene)-4-(2-phthalimidoethoxy)acetoacetate was dissolved in 102 ml of 2-propanol at 80° C. 33.1 g of ethyl-3-aminocrotonate was added and the mixture was heated at the same temperature for 16 hours. The mixture was evaporated to dryness. The residue was dissolved in 153 ml of glacial acetic acid at 80° C. The mixture was cooled to 15° C. and stirred at the same temperature for 20 hours. The solid was filtered off and washed with 78 ml of glacial acetic acid. The solid was suspended in 150 ml of methanol and agitated at 60° C. for 30 minutes. The solid was cooled to 20° C. and filtered off, washed with 30 ml of methanol and dried. The product was recrystallized from ethyl acetate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858738B2
出典データセットuspto-grants-2005_02
ORD IDord-249d482791444153aaceda86e7b6522a
出典メモuspto-grants-2005_02