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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42560생성일: 2026년 10월 24일

4-Methylmorpholine → N-Methoxy-6,N-dimethyl-nicotinamide

https://huagongshe.com/ko/reaction/42560

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
반응물6-Methylnicotinic acidHCID 137860—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
용매DimethylformamideHCID 6228—
생성물N-Methoxy-6,N-dimethyl-nicotinamideHCID 1136735329%

반응 단계

To a solution of 6-methylnicotinic acid (5.00 g, 36.5 mmol) in DMF (150 mL), 1-hydroxybenzotriazole (4.92 g, 36.5 mmol), N-ethyl-N-(3-dimethylaminopropyl) carbodiimide hydrochloride (8.38 g, 45.7 mmol) and 4-methylmorpholine (16.0 mL, 145.8 mmol) were added under argon atmosphere. The mixture was stirred at room temperature for 30 minutes after which N,O-dimethylhydroxylamine hydrochloride was added (3.55 g, 36.5 mmol). The reaction mixture was stirred at room temperature overnight. The solvent was evaporated off. The residue was dissolved in a mixture of CHCl3 and 0.2 N NaHCO3. The phases were separated and the aqueous phase was extracted with CHCl3. The organic phase was dried over Na2SO4 and concentrated to dryness. The product was purified by chromatography on silica gel using hexane-EtOAc mixtures of increasing polarity as eluent, to afford 1.11 g of the desired product (yield: 29%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536194B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-0ea530a68de14ebfa227f4f0f3b031f8
출처 메모uspto-grants-2013_09