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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 227060생성일: 2026년 10월 26일

3-Iodo-2,6-dimethylpyridine → 1-(6-Bromo-pyridin-2-ylmethyl)-3-(2,6-dimethyl-pyridine-3-carbonyl)-1H-quinolin-4-one

https://huagongshe.com/reaction/227060

반응식

참여 물질

역할이름HCID투입량
반응물3-Iodo-2,6-dimethylpyridineHCID 12999944—
반응물1-(6-Bromo-pyridin-2-ylmethyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid methoxy-methyl-amideHCID 57754532—
반응물HCID 178418918HCID 178418918—
용매TetrahydrofuranHCID 8028—
생성물1-(6-Bromo-pyridin-2-ylmethyl)-3-(2,6-dimethyl-pyridine-3-carbonyl)-1H-quinolin-4-oneHCID 57754656—

반응 단계

Experimental conditions analogous to those described for Step 6 of Example 60 from 105 mg (0.26 mmol) of 1-(6-bromo-pyridin-2-ylmethyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid methoxy-methyl-amide in 1 mL THF and 134 mg (0.58 mmol) of 2,6-dimethyl-5-iodo-pyridine in 1 mL THF with 0.30 mL 2M isopropylmagnesium chloride. Yield: 19 mg of a white powder. LC-MSD, m/z for C23H18BrN3O2 [M+H]+=448.0, 450.0; HPLC retention time: 1.2 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557213B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-8deebccf7b9943799fa99c0200df4d17
출처 메모uspto-grants-2009_07