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HRID 1591822作成日:2026年10月25日

Potassium Fluoride → 5-(4-amino-2-fluorophenyl)-1-methyl-1H-pyrrole-2-carbonitrile

https://huagongshe.com/reaction/1591822

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium FluorideHCID 522689—
反応物4-Bromo-3-fluoroanilineHCID 821848—
反応物(5-cyano-1-methyl-1H-pyrrol-2-yl)boronic acidHCID 11708078—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
生成物5-(4-amino-2-fluorophenyl)-1-methyl-1H-pyrrole-2-carbonitrileHCID 1605043298%

反応条件

温度25 °C

反応手順

4-Bromo-3-fluoroaniline (0.95 g, 5.0 mmol), 1-methyl-5-cyano-2-pyrroleboronic acid (1.35 g, 9.0 mmol), KF (0.96 g, 16.5 mmol), and Pd2(dba)3 (120 mg, 0.125 mmol) were added to a 50 mL round bottom flask under nitrogen. The flask was sealed and purged with nitrogen for 5 minutes. THF (12.5 mL) was added and the mixture was purged with nitrogen for an additional 5 minutes. A solution of tri-t-butylphosphine (10% wt in hexanes) (0.74 mL, 0.25 mmol) was added via syringe and the mixture was stirred vigorously at 25° C. for 16 hours. The mixture was diluted with 250 mL of EtOAc, filtered through a plug of silica gel, washed with 200 mL of EtOAc and concentrated to give a crude brown/black semi-solid. Purification via Isco chromatography (the Redisep® column, silica, gradient 5%-100% ethyl acetate in hexane) afforded 5-(4-amino-2-fluorophenyl)-1-methyl-1H-pyrrole-2-carbonitrile as a white solid (1.05 g, 98%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07291643B2
出典データセットuspto-grants-2007_11
ORD IDord-f2219bb2c98e4fb2b4debed68b0be904
出典メモuspto-grants-2007_11