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HRID 1521700作成日:2026年10月25日

Ethanol → HCID 67236396、化合物

https://huagongshe.com/reaction/1521700

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Sodium AcetateHCID 517045—
反応物Ethyl 6-chloro-1H-pyrrolo[2,3-b]pyridine-2-carboxylateHCID 21868758—
反応物HCID 178418416HCID 178418416—
触媒palladium(II) acetateHCID 167845—
触媒Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
生成物HCID 67236396HCID 67236396—

反応条件

温度110 °C

反応手順

Reagents are charged into a 600 mL autoclave in the following order: ethanol (350 mL), sodium acetate (17.0 g, 200 mmol), 6-chloro-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid ethyl ester (24 g, 107 mmol), 1,1′-bis-(diphenylphosphino)ferrocene (2.5 g, 2.25 mmol [2.25 mol %]), and palladium acetate (180 mg, 0.75 mmol [0.75 mol %]). The air in the autoclave is replaced with carbon monoxide and the pressure is adjusted to 250 psi. The reaction is then heated to 110° C. for 15 h. The reaction mixture is cooled to room temperature and is filtered through Celite. The solvent is replaced with 500 mL EtOAc followed by 100 mL aqueous wash. The organic layer is concentrated to 50 mL EtOAc and is then heated to 60° C. After cooling to room temperature, the solids are filtered to afford 20 g of the title compound. The mother liquor is concentrated and is purified by flash column chromatography using gradient elution of 20-60% ethyl acetate in hexanes to afford an additional 3.5 g of title compound which affords total of 23.5 g in 84% isolated yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09073926B2
出典データセットuspto-grants-2015_07
ORD IDord-32c0f72e8d024636bd4aefb4ea9ec82e
出典メモuspto-grants-2015_07