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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 247113생성일: 2026년 10월 25일

3-Nitrobenzaldehyde → Methyl 1,4-dihydro-2,6-dimethyl-3-(3-chloromethyl-1,2,4-oxadiazol-5-yl)-4-(3-nitrophenyl)pyridine-5-carboxylate

https://huagongshe.com/reaction/247113

반응식

참여 물질

역할이름HCID투입량
반응물3-NitrobenzaldehydeHCID 7449—
반응물Methyl 3-aminocrotonateHCID 643918—
반응물5-Acetonyl-3-chloromethyl-1,2,4-oxadiazoleHCID 13824705—
용매IsopropanolHCID 3776—
생성물Methyl 1,4-dihydro-2,6-dimethyl-3-(3-chloromethyl-1,2,4-oxadiazol-5-yl)-4-(3-nitrophenyl)pyridine-5-carboxylateHCID 13583341663.7%

반응 단계

A solution of 8.0 g of 5-acetonyl-3-chloromethyl-1,2,4-oxadiazole, 6.92 g of 3-nitrobenzaldehyde and 5.27 g of methyl 3-aminocrotonate in 20 ml of isopropyl alcohol was heated under reflux for 6 hours. After ice-cooling, the precipitated solid was collected by filtration, washed with cold isopropyl alcohol and dried to give 11.8 g of methyl 1,4-dihydro-2,6-dimethyl-3-(3-chloromethyl-1,2,4-oxadiazol-5-yl)-4-(3-nitrophenyl)pyridine-5-carboxylate as yellow crystals, m.p. 200.5°-201.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04705786
출처 데이터셋uspto-grants-1987_11
ORD IDord-9cb3060ce6c548bf914909ad65d20b68
출처 메모uspto-grants-1987_11