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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 606312생성일: 2026년 10월 25일

Dimethylformamide → 1-Chloro-6-methoxy-3-methyl-isoquinoline-4-carbaldehyde

https://huagongshe.com/reaction/606312

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물4-Bromo-1-chloro-6-methoxy-3-methylisoquinolineHCID 86615932—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1-Chloro-6-methoxy-3-methyl-isoquinoline-4-carbaldehydeHCID 8661593372.4%

반응 조건

온도0 °C

반응 단계

n-BuLi (12 ml of 1.6 M in hexane) is added dropwise to a solution of 4-bromo-1-chloro-6-methoxy-3-methyl-isoquinoline (4.8 g, 17 mmol) in THF (60 ml) at −78° C. After stirring for 40 min, DMF (4 ml, 51 mmol) is added slowly. The reaction is allowed to warm to 0° C. and the stirring is continued for 1 h. The mixture is then quenched with 1N—HCl (30 ml) and extracted with EtOAc. The combined extracts are dried over Na2SO4 and evaporated. The residue is chromatographed on silica gel eluting with EtOAc/hexane (1:4) to give 2.9 g of 1-chloro-6-methoxy-3-methyl-isoquinoline-4-carbaldehyde. 1H NMR (CDCl3) 10.8 (s, 1H), 8.61 (s, 1H), 8.24 (d, 1H), 7.29 (d, 1H), 4.01 (s, 3H), 2.99 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07915288B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-430a20bdee074d54a2da199c33df1690
출처 메모uspto-grants-2011_03