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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1616071생성일: 2026년 10월 27일

2-Amino-5-fluoro-N-methoxy-N-methylbenzamide → 3-Methylpyridine-2-carboxaldehyde

https://huagongshe.com/reaction/1616071

반응식

참여 물질

역할이름HCID투입량
반응물2-Amino-5-fluoro-N-methoxy-N-methylbenzamideHCID 53407572—
반응물HCID 178418918HCID 178418918—
반응물HCID 178426302HCID 178426302—
용매TetrahydrofuranHCID 8028—
생성물3-Methylpyridine-2-carboxaldehydeHCID 1501874—

반응 단계

To a solution of 2-amino-5-fluoro-N-methoxy-N-methylbenzamide (1.0 g, 5.05 mmol) in THF (4.2 mL) was added isopropylmagnesium chloride (2.0M in THF, 5.0 mL, 10.1 mmol) at −40° C. The temperature was allowed to rise to −10° C. over 40 min then was lowered to −40° C. in an acetonitrile/dry ice bath. 3-Methyl-2-pyridinylmagnesium bromide (0.25M in THF, 20.2 mL, 5.0 mmol) was added dropwise and the solution was allowed to rise to rt over one hour. The solution was partitioned between satd ammonium chloride solution and DCM; organic extracts were concentrated then purified by silica gel column chromatography eluting with a gradient of 10-70% EtOAc in hexane to afford 2-amino-5-fluorophenyl)(3-methylpyridin-2-yl)methanone as a yellow oil: LC-MS (ESI) m/z 231.2 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08765768B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-093185e68e544071a1aec297b85ac95c
출처 메모uspto-grants-2014_07