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HRID 29507作成日:2026年10月26日

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

https://huagongshe.com/reaction/29507

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物4-CyanopyridineHCID 7506—
反応物Sodium HydroxideHCID 14798—
反応物Boron TrichlorideHCID 25135—
反応物3,4-DifluoroanilineHCID 77469—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒TrichloroethyleneHCID 6575—
生成物(2-Amino-4,5-difluoro-phenyl)-pyridin-4-yl-methanoneHCID 22327317—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07420055B2
出典データセットuspto-grants-2008_09
ORD IDord-590fb90e5aed4c9387b4cf70831341c8
出典メモuspto-grants-2008_09