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HRID 25475作成日:2026年10月26日

Methyl 3-aminocrotonate → Phthalimidoamlodipine

https://huagongshe.com/reaction/25475

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Ethyl 2-(2-chlorobenzylidene)-4-(2-(1,3-dioxoisoindolin-2-yl)ethoxy)-3-oxobutanoateHCID 53879087—
溶媒IsopropanolHCID 3776—
生成物PhthalimidoamlodipineHCID 9871958—

反応条件

温度15 °C

反応手順

350 g of crude ethyl 2-(o-chlorobenzylidene)-4-(2-phthalimidoethoxy) acetoacetate from Example 1 was dissolved in 540 ml of 2-propanol at 80° C. 50 g of methyl-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 540 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 formed solid was filtered off and washed with 280 ml of glacial acetic acid. The solid was suspended in 225 ml of methanol and agitated for 30 minutes. The solid was filtered off, washed with 75 ml of methanol and dried.

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-373b8316f2424a3bbbfd26a259af20b1
出典メモuspto-grants-2005_02