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HRID 227060作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物3-Iodo-2,6-dimethylpyridineHCID 12999944—
反応物1-(6-Bromo-pyridin-2-ylmethyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid methoxy-methyl-amideHCID 57754532—
反応物HCID 178418918HCID 178418918—
溶媒TetrahydrofuranHCID 8028—
生成物1-(6-Bromo-pyridin-2-ylmethyl)-3-(2,6-dimethyl-pyridine-3-carbonyl)-1H-quinolin-4-oneHCID 57754656—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07557213B2
出典データセットuspto-grants-2009_07
ORD IDord-8deebccf7b9943799fa99c0200df4d17
出典メモuspto-grants-2009_07