돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 247114생성일: 2026년 10월 26일

3-Nitrobenzaldehyde → 2-(n-Propoxy)ethyl 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/247114

반응식

참여 물질

역할이름HCID투입량
반응물3-NitrobenzaldehydeHCID 7449—
반응물2-(n-Propoxy)ethyl 3-aminocrotonateHCID 12529190—
반응물5-Acetonyl-3-chloromethyl-1,2,4-oxadiazoleHCID 13824705—
용매IsopropanolHCID 3776—
생성물2-(n-Propoxy)ethyl 1,4-dihydro-2,6-dimethyl-3-(3-chloromethyl-1,2,4-oxadiazol-5-yl)-4-(3-nitrophenyl)pyridine-5-carboxylateHCID 13583342495.1%

반응 단계

A mixture of 530 mg of 5-acetonyl-3-chloromethyl-1,2,4-oxadiazole, 450 mg of 3-nitrobenzaldehyde and 560 mg of 2-(n-propoxy)ethyl 3-aminocrotonate in 3 ml of isopropyl alcohol was heated under reflux for 8 hours. The reaction mixture was concentrated in vacuo and the residue was chromatographed on silica gel using benzene-acetonitrile (10:1) as eluent to give 1.35 g of 2-(n-propoxy)ethyl 1,4-dihydro-2,6-dimethyl-3-(3-chloromethyl-1,2,4-oxadiazol-5-yl)-4-(3-nitrophenyl)pyridine-5-carboxylate. Recrystallization from n-hexane-isopropylalcohol afforded pale yellow crystals, m.p. 129°-130° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04705786
출처 데이터셋uspto-grants-1987_11
ORD IDord-cdf59e3109a848d0a79f78a5454db494
출처 메모uspto-grants-1987_11