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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 349269생성일: 2026년 10월 23일

3-(Tributylstannyl)pyridine → 1-(3,5-Bis-trifluoromethyl-benzyl)-5-pyridin-3-yl-1H-imidazole-4-carbonitrile

https://huagongshe.com/ko/reaction/349269

반응식

참여 물질

역할이름HCID투입량
반응물3-(Tributylstannyl)pyridineHCID 3483848—
반응물1-(3,5-Bis-trifluoromethyl-benzyl)-5-iodo-1H-imidazole-4-carbonitrileHCID 86601222—
촉매Bis(benzonitrile)palladium chlorideHCID 498840—
용매AcetonitrileHCID 6342—
생성물1-(3,5-Bis-trifluoromethyl-benzyl)-5-pyridin-3-yl-1H-imidazole-4-carbonitrileHCID 86601221—

반응 단계

In a pressure vessel dissolve 1-(3,5-Bis-trifluoromethyl-benzyl)-5-iodo-1H-imidazole-4-carbonitrile (0.52 g, 1.2 mmol) in acetonitrile. Add 3-tributylstannanyl-pyridine (0.64 g, 1.7 mmol) and bis(benzonitrile)dichloropalladium(II) (22 mg, 0.06 mmol), and stir at 100° C. After 72 h, quench with sat. aq. NaHCO3, and extract with ether. Wash the organic layer with brine, dry over MgSO4, filter, and concentrate. Purify by radial chromatography on silica gel to give the title compound: MS (ES) 397.2 (M+1); 1H NMR (300 MHz, CDCl3) δ 8.75 (d, J=4.6 Hz, 1H), 8.60 (ap d, 1H), 7.84 (s, 1H), 7.75 (s, 1H), 7.66 (m, 1H), 7.44 (m, 1H), 7.36 (s, 2H), 5.30 (s, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07179804B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-cc72bbe93a664215aa1a6308b75d81c9
출처 메모uspto-grants-2007_02