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HRID 25477作成日:2026年10月24日

Methyl 3-aminocrotonate → 4-(2-Chlorophenyl)-2-[[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)ethoxy]methyl]-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylic Acid 3,5-Dimethyl Ester

https://huagongshe.com/ja/reaction/25477

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 3-aminocrotonateHCID 643918—
反応物Methyl 2-(o-chlorobenzylidene)-4-(2-phthalimidoethoxy)acetoacetateHCID 69267975—
溶媒IsopropanolHCID 3776—
生成物4-(2-Chlorophenyl)-2-[[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)ethoxy]methyl]-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylic Acid 3,5-Dimethyl EsterHCID 11260992—

反応条件

温度15 °C

反応手順

92.1 g of methyl 2-(o-chlorobenzylidene)-4-(2-phthalimidoethoxy)acetoacetate was dissolved in 108 ml of 2-propanol at 80° C. 31.3 g of methyl-3-aminocrotonate was added and the mixture was heated at the same temperature for 24 hours. The mixture was evaporated to dryness. The residue was dissolved in 162 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 83 ml of glacial acetic acid. The solid was suspended in 68 ml of methanol and agitated for 30 minutes. The solid was filtered off, washed with 23 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-37af752ca5b5457c9f1e81b7de7d9e72
出典メモuspto-grants-2005_02