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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1108104생성일: 2026년 10월 26일

1-(4-iodophenyl)-2-methyl-1H-imidazole → (2SR,4RS)-4-cyano-2-methyl-4-[3-[4-(2-methylimidazol-1-yl) phenylthio]phenyl]-3,4,5,6-tetrahydro-2H-pyran

https://huagongshe.com/reaction/1108104

반응식

참여 물질

역할이름HCID투입량
반응물1-(4-iodophenyl)-2-methyl-1H-imidazoleHCID 11289090—
반응물(2SR,4RS)-4-cyano-2-methyl-4-(3-triisopropylsilylthiophenyl)-3,4,5,6-tetrahydro-2H-pyranHCID 18786333—
반응물Potassium tert-butoxideHCID 23665647—
촉매HCID 178418397HCID 178418397—
용매EthanolHCID 702—
생성물(2SR,4RS)-4-cyano-2-methyl-4-[3-[4-(2-methylimidazol-1-yl) phenylthio]phenyl]-3,4,5,6-tetrahydro-2H-pyranHCID 1878634793%

반응 단계

To a stirred solution of 4-(2-methylimidazol-1-yl)phenyl iodide (1.21 g, 3.1 mmol) and (2SR, 4RS)-4-cyano-2-methyl-4-(3-triisopropylsilylthiophenyl)-3,4,5,6-tetrahydro-2H-pyran (795 mg, 2.8 mmol) in ethanol (20 ml) was added tetrakis(triphenylphosphine)palladium(0) (215 mg, 0.2 mmol) and potassium tert-butoxide (383 mg, 3.4 mmol) under a nitrogen atmosphere. The resulting mixture was heated at reflux temperature for 15.5 h, then cooled and concentrated in vacuo. The residue was diluted in ethyl acetate (100 ml), and washed with water (2×100 ml), brine (100 ml) and dried (MgSO4) and concentrated. Purification by silica-gel column chromatography, eluting with dichloromethane-methanol (25:1), gave 1.01 g (93%) of the titled compound as a yellow gum.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06063928
출처 데이터셋uspto-grants-2000_05
ORD IDord-62c4e6a5333c4a5284ecabf7faca1a04
출처 메모uspto-grants-2000_05