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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 542237생성일: 2026년 10월 26일

3-Nitrobenzaldehyde → 2-(4-Acetylaminobenzoyloxy)ethyl 2,6-dimethyl-5-ethoxycarbonyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/542237

반응식

참여 물질

역할이름HCID투입량
반응물3-NitrobenzaldehydeHCID 7449—
반응물2-Butenoic acid, 3-amino-, ethyl ester, (2Z)-HCID 643756—
반응물2-(4-Acetylaminobenzoyloxy)ethyl acetylacetateHCID 20151269—
용매EthanolHCID 702—
생성물2-(4-Acetylaminobenzoyloxy)ethyl 2,6-dimethyl-5-ethoxycarbonyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylateHCID 2015128046%

반응 조건

온도-5 °C

반응 단계

20 g (0.07 moles) of 2-(4-acetylaminobenzoyloxy)ethyl acetylacetate, 8.41 g (0.07 moles) of ethyl 3-aminocrotonate and 9.84 g (0.07 moles) of 3-nitrobenzaldehyde are heated under reflux in 65 ml of ethanol for 8 hours. The solvent is then evaporated, 15 ml of boiling methanol are added to the residue, the solution is discoloured with activated charcoal and cooled to -5° C. to obtain 2-(4-acetylaminobenzoyloxy)ethyl 2,6-dimethyl-5-ethoxycarbonyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate with half a molecule of ethanol as yellow crystals melting--after recrystallisation in ethanol--at 157°-162° C. The yield is 46% of the theoretical yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04656181
출처 데이터셋uspto-grants-1987_04
ORD IDord-3f96357e28524010b415e2a09d4494b8
출처 메모uspto-grants-1987_04