돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1007204생성일: 2026년 10월 24일

Methyl iodide → 6-Chloro-N-(4-ethoxy-2-nitrophenyl)-N-methyl-3-pyridinecarboxamide

https://huagongshe.com/ko/reaction/1007204

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물6-Chloro-N-(4-ethoxy-2-nitrophenyl)-3-pyridinecarboxamideHCID 9840127—
반응물Sodium MethoxideHCID 10942334—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물6-Chloro-N-(4-ethoxy-2-nitrophenyl)-N-methyl-3-pyridinecarboxamideHCID 9902284—

반응 단계

To a solution of 6-chloro-N-(4-ethoxy-2-nitrophenyl)-3-pyridinecarboxamide (50 mg, 0.155 mmol) in DMF (2 ml) was added sodium methoxide (12 mg, 0.222 mmol) in DMF (1 ml) and the reaction mixture was stirred for 10 min. To the mixture was added iodomethane (22 mg, 0.155 mmol) slowly and the mixture was stirred for at room temperature for 3 h. It was diluted with ethyl acetate and washed with water and brine, dried over anhydrous sodium sulfate, and evaporated. The residue was purified by column chromatography to yield the titled compound as a light brown liquid. 1H NMR (CDCl3): 8.17 (d, J=2.1, 1H), 7.68-7.65 (m, 1H), 7.35 (d, J=2.7, 1H), 7.21 (t, J=7.8, 2H), 7.10-7.06 (m, 1H), 4.08-4.01 (m, 2H), 3.40 (s, 3H), 1.44 (t, J=6.9, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06794397B2
출처 데이터셋uspto-grants-2004_09
ORD IDord-2e9b5a0cb09742b5b398e9734a4ad3dd
출처 메모uspto-grants-2004_09