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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31914생성일: 2026년 10월 26일

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → Ethyl 2-(4-cyanophenyl)-6-({2-[(5-nitro(2-pyridyl))amino]ethyl}amino)pyridine-3-carboxylate

https://huagongshe.com/reaction/31914

반응식

참여 물질

역할이름HCID투입량
반응물2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
반응물2-ChloropyridineHCID 7977—
반응물Ethyl 3-(4-Cyanophenyl)-3-oxopropionateHCID 2757969—
반응물{2-[(6-Amino-5-nitro(2-pyridyl))amino]ethyl}[6-(2,4-dichlorophenyl)-5-imidazolyl(2-pyridyl)]amineHCID 22142808—
반응물Ethyl 6-chloro-2-phenylpyridine-3-carboxylateHCID 22142863—
용매TolueneHCID 1140—
용매DimethylacetamideHCID 31374—
용매Tetrahydrofuran ethanolHCID 21873804—
생성물Ethyl 2-(4-cyanophenyl)-6-({2-[(5-nitro(2-pyridyl))amino]ethyl}amino)pyridine-3-carboxylateHCID 22142398—

반응 단계

ethyl 2-(4-cyanophenyl)-6-({2-[(5-nitro(2-pyridyl))amino]ethyl}amino)pyridine-3-carboxylate (62258) was prepared from ethyl 3-(4-cyanophenyl)-3-oxopropanoate (ref. Wemple, J.; et. al. Synthesis 1993, 290-292.) as the starting material and THF/ethanol ratio of 1:5 as the solvent in the first step. The oxidation uses DDQ in toluene. The final product is achieved directly from the chloropyridine by reacting ethyl 6-chloro-2-phenylpyridine-3-carboxylate with 2-(2-aminoethylamine)-5-nitropyridine in DMA and Hüing's base at 120° C. for 18 hours. The procedures are analogous to the general method for {2-[(6-amino-5-nitro(2-pyridyl))amino]ethyl}[6-(2,4-dichlorophenyl)-5-imidazolyl(2-pyridyl)]amine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425557B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-db97e95694fc4cb7baa6d62880ce223a
출처 메모uspto-grants-2008_09