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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 406444생성일: 2026년 10월 25일

1-Ethynyl-4-(trifluoromethyl)benzene → 3-(1,1-Difluoro-2-methoxyethyl)-6-((4-(trifluoromethyl)phenyl)ethynyl)-[1,2,4]triazolo[4,3-a]pyridine

https://huagongshe.com/reaction/406444

반응식

참여 물질

역할이름HCID투입량
반응물1-Ethynyl-4-(trifluoromethyl)benzeneHCID 4348295—
반응물6-Bromo-3-(1,1-difluoro-2-methoxyethyl)-[1,2,4]triazolo[4,3-a]pyridineHCID 58118956—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매TetrahydrofuranHCID 8028—
생성물3-(1,1-Difluoro-2-methoxyethyl)-6-((4-(trifluoromethyl)phenyl)ethynyl)-[1,2,4]triazolo[4,3-a]pyridineHCID 50908330—

반응 조건

온도70 °C

반응 단계

To a stirred solution of 6-bromo-3-(1,1-difluoro-2-methoxyethyl)-[1,2,4]triazolo[4,3-a]pyridine (46 mg, 0.16 mmol) in THF (5 mL) was added catalytic amount of dichlorobis(triphenylphosphine) palladium(II) (11 mg) and copper(I) iodide (3 mg), followed by 1-ethynyl-4-(trifluoromethyl)benzene (41 mg, 0.24 mmol). The resulting mixture was flushed with N2 and Et3N (2 mL) was added. The reaction mixture was stirred at 70° C. overnight and purified by prep-TLC (EtOAc: hexanes=2:3) followed by HPLC to give 3-(1,1-difluoro-2-methoxyethyl)-6-((4-(trifluoromethyl)phenyl)ethynyl)-[1,2,4]triazolo[4,3-a]pyridine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754103B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-b90f0c8d8a514419babce827e758a1e5
출처 메모uspto-grants-2014_06