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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1591822생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1591822

반응식

참여 물질

역할이름HCID투입량
반응물Potassium FluorideHCID 522689—
반응물4-Bromo-3-fluoroanilineHCID 821848—
반응물(5-cyano-1-methyl-1H-pyrrol-2-yl)boronic acidHCID 11708078—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
생성물5-(4-amino-2-fluorophenyl)-1-methyl-1H-pyrrole-2-carbonitrileHCID 1605043298%

반응 조건

온도25 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07291643B2
출처 데이터셋uspto-grants-2007_11
ORD IDord-f2219bb2c98e4fb2b4debed68b0be904
출처 메모uspto-grants-2007_11