돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1271564생성일: 2026년 10월 26일

1,3-Difluoro-5-iodobenzene → (2-(3,5-Difluoro-phenylethynyl)-6-methyl-pyridin-3-yl)amine

https://huagongshe.com/reaction/1271564

반응식

참여 물질

역할이름HCID투입량
반응물1,3-Difluoro-5-iodobenzeneHCID 2778221—
반응물2-Ethynyl-6-methylpyridin-3-amineHCID 18454776—
촉매HCID 178418476HCID 178418476—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물(2-(3,5-Difluoro-phenylethynyl)-6-methyl-pyridin-3-yl)amineHCID 1033205858%

반응 단계

To a solution of Cul (4.3 mg, 23 μmol) in triethylamine (5 ml) were added (2-ethynyl-6-methyl-pyridin-3-yl)amine (60 mg, 0.45 mmol), (PPh3)2PdCl2 (16 mg, 23 μmol), and 1,3-difluoro-5-iodobenzene (109 mg, 0.45 mmol). The reaction mixture was stirred at room temperature for 20 h. The solvent was evaporated to afford a brown oil which was taken up in DCM and the solution was washed with water. The aqueous phase was extracted twice with DCM. The organic phases were dried over Na2SO4, filtered and concentrated. The crude residue was purified by flash chromatography (hexane/ethyl acetate 7:3) to yield 64 mg (0.26 mmol, 58%) of (2-(3,5-difluoro-phenylethynyl)-6-methyl-pyridin-3-yl)amine as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07205411B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-99b7ae33a07f4627bf712d9e7b4b48c1
출처 메모uspto-grants-2007_04