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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25479생성일: 2026년 10월 25일

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

반응식

참여 물질

역할이름HCID투입량
반응물2-Butenoic acid, 3-amino-, ethyl ester, (2Z)-HCID 643756—
반응물Methyl 2-(o-chlorobenzylidene)-4-(2-phthalimidoethoxy)acetoacetateHCID 69267975—
용매IsopropanolHCID 3776—
생성물3-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—

반응 조건

온도15 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858738B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-249d482791444153aaceda86e7b6522a
출처 메모uspto-grants-2005_02