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HRID 29507생성일: 2026년 10월 25일

Hydrochloric Acid → (2-Amino-4,5-difluoro-phenyl)-pyridin-4-yl-methanone

https://huagongshe.com/reaction/29507

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-CyanopyridineHCID 7506—
반응물Sodium HydroxideHCID 14798—
반응물Boron TrichlorideHCID 25135—
반응물3,4-DifluoroanilineHCID 77469—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매TrichloroethyleneHCID 6575—
생성물(2-Amino-4,5-difluoro-phenyl)-pyridin-4-yl-methanoneHCID 22327317—

반응 단계

BCl3 (6.2 ml, 1M in DCM) was added drop wise to 1,2-difluoro-4aminobenzene (0.5 g, 0.004 mol) in trichloroethylene (6.5 ml) at 0° C. and this mixture stirred for 15 min. 4-Cyanopyridine (0.48 g, 0.005 mol) was added and the solution was warmed to RT and stirred for 30 min. The solution was then heated at 80-90° C. for 1 h. The resulting solution was refluxed at 160° C. for 4 hr and stirred at RT over night. 3N HCl was added to the reaction mixture and refluxed at 110° C. for 1.5 h. The reaction mixture was cooled to RT and made basic (pH=12) with 6N NaOH. The reaction mixture was diluted with water and DCM. The resulting two layers were separated and the aqueous layer was extracted with DCM, dried over sodium sulphate and concentrated. The compound was purified by column chromatography using silica gel to yield title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420055B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-590fb90e5aed4c9387b4cf70831341c8
출처 메모uspto-grants-2008_09