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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 322205생성일: 2026년 10월 24일

4-Amino-3-penten-2-one → 5-Acetyl-2-(4-azidobutyl)-3-(2-cyanoethoxy)carbonyl-1,4-dihydro-6-methyl-4-(4-nitrophenyl)pyridine

https://huagongshe.com/ko/reaction/322205

반응식

참여 물질

역할이름HCID투입량
반응물4-Amino-3-penten-2-oneHCID 136873—
반응물7-Azido-2-[(4-nitrophenyl)methylene]-3-oxoheptanoic acid 2-cyanoethyl esterHCID 53869981—
용매EthanolHCID 702—
생성물5-Acetyl-2-(4-azidobutyl)-3-(2-cyanoethoxy)carbonyl-1,4-dihydro-6-methyl-4-(4-nitrophenyl)pyridineHCID 23004053—

반응 단계

A solution of 7-azido-2-[(4-nitrophenyl)methylene]-3-oxoheptanoic acid 2-cyanoethyl ester (1.12 g, 3.00 mmol) and 4-amino-3-penten-2-one (330 mg, 3.30 mmol) in 20 ml of EtOH was refluxed for 48 hrs. After the EtOH was removed in vacuo, the residue was dissolved in 150 ml of CHCl3, washed with water (2×100 ml) and dried over Na2SO4. After filtration and evaporation of solvent, the product was purified by chromatography (SiO2, CHCl3:MeOH=5:95). 5-Acetyl-2-(4-azidobutyl)-3-(2-cyanoethoxy) carbonyl-1,4-dihydro-6-methyl-4-(4-nitrophenyl) pyridine was obtain as a yellow oil (1.05 g, 77% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06211198B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-e12c3f792d634edd96bdda7e971c28c5
출처 메모uspto-grants-2001_04