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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 270693생성일: 2026년 10월 25일

4-Aminonicotinaldehyde → 2-(2,6-dichloro-3-nitro-phenyl)-N-(3-formyl-pyridin-4-yl)-acetamide

https://huagongshe.com/reaction/270693

반응식

참여 물질

역할이름HCID투입량
반응물4-AminonicotinaldehydeHCID 2761033—
반응물2,6-Dichloro-3-nitrophenylacetic acidHCID 54265437—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
용매Thionyl ChlorideHCID 24386—
생성물2-(2,6-dichloro-3-nitro-phenyl)-N-(3-formyl-pyridin-4-yl)-acetamideHCID 5983385995.2%

반응 단계

A solution of (2,6-dichloro-3-nitro-phenyl)-acetic acid (15.0 g, 60.0 mmol) in thionyl chloride (60 mL) is refluxed for one hour. The solvent is removed by concentration; dry toluene is added and concentrated to thoroughly remove thionyl chloride. To the solution of acid chloride in dry dichloromethane (200 mL) is added (drop-wise) a solution of 4-amino-pyridine-3-carbaldehyde (6.6 g, 54 mmol) in dichloromethane (50 mL) and DIEDA (10.7 mL, 60 mmol). The mixture is at room temperature for 2 hours. The reaction mixture is diluted with EtOAc (300 ml) and washed with saturated K2CO3 and brine. The organic layer is dried, filtered and concentrated to give crude product. Recrystallization with dichloromethane/hexane results in the titled compound as a solid (18.2 g, 95.2%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07449582B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-c0ea74fc44c74a67a44b70cbc2269a15
출처 메모uspto-grants-2008_11