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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25475생성일: 2026년 10월 24일

Methyl 3-aminocrotonate → Phthalimidoamlodipine

https://huagongshe.com/ko/reaction/25475

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 3-aminocrotonateHCID 643918—
반응물Ethyl 2-(2-chlorobenzylidene)-4-(2-(1,3-dioxoisoindolin-2-yl)ethoxy)-3-oxobutanoateHCID 53879087—
용매IsopropanolHCID 3776—
생성물PhthalimidoamlodipineHCID 9871958—

반응 조건

온도15 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858738B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-373b8316f2424a3bbbfd26a259af20b1
출처 메모uspto-grants-2005_02