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HRID 550891作成日:2026年10月26日

Methane → ethyl 3-(4-aminophenyl)-1H-pyrrolo[2,3-c]pyridine-2-carboxylate

https://huagongshe.com/reaction/550891

反応式

関与物質

役割名称HCID仕込み量
反応物MethaneHCID 297—
反応物Potassium FluorideHCID 522689—
反応物(4-Aminophenyl)boronic acid hydrochlorideHCID 2734614—
反応物ethyl 3-bromo-1H-pyrrolo[2,3-c]pyridine-2-carboxylateHCID 57445353—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒TriethylamineHCID 8471—
溶媒1,4-DioxaneHCID 31275—
生成物ethyl 3-(4-aminophenyl)-1H-pyrrolo[2,3-c]pyridine-2-carboxylateHCID 5744535257.4%

反応手順

To a solution of 1 g of ethyl 3-bromo-1H-pyrrolo[2,3-c]pyridine-2-carboxylate in 100 mL of dioxane are added 773 mg of 4-aminophenylboronic acid hydrochloride and 1.1 g of potassium fluoride in 9 mL of water. The reaction mixture is stirred under an argon atmosphere for 15 minutes. 425 mg of tetrakis(triphenylphosphine)palladium(0) and 630 μL of triethylamine are added. The reaction mixture is stirred for 17 hours at reflux. After treating with carbon black and then filtering through Celite®, the filtrate is concentrated under reduced pressure. The residue is purified by flash chromatography on a column of silica (60; 35-70 μM), eluting with a mixture of dichloromethane, methanol and acetonitrile (90/5/5 by volume). 600 mg of ethyl 3-(4-aminophenyl)-1H-pyrrolo[2,3-c]pyridine-2-carboxylate are obtained, the characteristics of which are as follows:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07947706B2
出典データセットuspto-grants-2011_05
ORD IDord-cb85bc5963f54265acc359ec33f26a0a
出典メモuspto-grants-2011_05