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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 83288생성일: 2026년 10월 24일

Dimethyl Sulfoxide → Methyl 6-(((5-methyl-3-phenylisoxazol-4-yl)methyl)amino)nicotinate

https://huagongshe.com/ko/reaction/83288

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물DiisopropylethylamineHCID 81531—
반응물Methyl 6-chloropyridine-3-carboxylateHCID 254249—
반응물(5-Methyl-3-phenyl-4-isoxazolyl)-methylamineHCID 59594513—
용매Ethyl AcetateHCID 8857—
생성물Methyl 6-(((5-methyl-3-phenylisoxazol-4-yl)methyl)amino)nicotinateHCID 6844353946.1%

반응 조건

온도160 °C

반응 단계

A mixture of (5-methyl-3-phenyl-4-isoxazolyl)-methylamine (200 mg, 1.06 mmol), methyl 6-chloronicotinate (182 mg, 1.06 mmol), N,N-diisopropyl ethyl amine (364 μL, 2.13 mmol) and DMSO (2 mL) was heated in the microwave to 160° C. for 0.5 h. It was diluted with ethyl acetate (8 mL) and washed with aqueous sodium carbonate (saturated, 8 mL), water (8 mL) and brine (8 mL). The combined aqueous layers were extracted with ethyl acetate (10 mL) and the combined organic layers were dried over sodium sulfate. Concentration and purification by chromatography (SiO2, heptane:ethyl acetate=100:0 to 50:50) afforded the title compound (158 mg, 46%) as a light yellow oil. MS: m/e=324.3 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846719B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-d6f0e4ff98fb4548b255d2fe6f0dd391
출처 메모uspto-grants-2014_09