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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 627485생성일: 2026년 10월 25일

Triethylamine → N-Methoxy-N-methyl-2-(trifluoromethyl)isonicotinamide

https://huagongshe.com/reaction/627485

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ammonium ChlorideHCID 25517—
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
반응물2-(Trifluoromethyl)pyridine-4-carboxylic acidHCID 14761447—
반응물HCID 178458058HCID 178458058—
용매DichloromethaneHCID 6344—
생성물N-Methoxy-N-methyl-2-(trifluoromethyl)isonicotinamideHCID 86716069—

반응 단계

To a suspension of 2-(trifluoromethyl)isonicotinic acid (1.03 g, 5.39 mmol), N,O-dimethylhydroxylamine hydrochloride (0.800 g, 8.20 mmol), N′(ethylcarbonimidoyl)-N,N-dimethyl-1,3-propanediamine hydrochloride (EDCI, 1.35 g, 7.04 mmol) and CH2Cl2 was added Et3N (1.90 mL, 13.7 mmol), and the mixture immediately turned to clear. After stirring at room temperature overnight, NH4Cl (aqueous) was added. The mixture was stirred vigorously for a while, and white solid was filtered off. The organic layer was separated, and the aqueous layer was extracted with CH2Cl2. The combined organic phases were washed with brine, and the aqueous layer was back extracted with CH2Cl2. The organic phase was dried (Na2SO4), filtered, concentrated, and purified by flash column chromatography (40 g silica gel column, 40-70% EtOAc in heptanes) to give the title compound as a clear oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09309222B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-235aeff638e64e1f991c0d1977caebea
출처 메모uspto-grants-2016_04