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HRID 13274作成日:2026年10月25日

Sodium Carbonate → t-Butyl 2-(2-fluoro-5-nitro-phenyl)-pyrrole-1-carboxylate

https://huagongshe.com/reaction/13274

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物2-Bromo-1-fluoro-4-nitrobenzeneHCID 69699—
反応物Sodium BicarbonateHCID 516892—
反応物1-(tert-Butoxycarbonyl)-2-pyrroleboronic AcidHCID 2734321—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物t-Butyl 2-(2-fluoro-5-nitro-phenyl)-pyrrole-1-carboxylateHCID 23145764—

反応手順

1.1 g of tetrakis-triphenylphosphine palladium and 4.2 g of sodium carbonate were added to a solution of 4.3 g of 3-bromo-4-fluoro-nitrobenzene and 5.0 g of 1-(t-butoxycarbonyl)pyrrole-2-boronic acid in a mixture of 130 ml of dimethoxyethane and 22 ml of water, and the reaction liquid was heated overnight under reflux. Aqueous saturated sodium bicarbonate was added to the reaction liquid, and this was extracted with ethyl acetate. The organic layer was washed with water and saturated saline in order, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=20/1) to obtain the entitled compound as a yellow oily substance.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728025B2
出典データセットuspto-grants-2010_06
ORD IDord-5b2c7caafde048c49c5bbc8275c188f1
出典メモuspto-grants-2010_06