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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1685664생성일: 2026년 10월 27일

Ethyl Acetate → 4-{[2-(3-Hydroxy-phenylsulfanyl)-ethyl]-[1,2,4]triazol-4-yl-amino}-benzonitrile

https://huagongshe.com/reaction/1685664

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참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Potassium CarbonateHCID 11430—
반응물4-[(2-Bromo-ethyl)-[1,2,4]triazol-4-yl-amino]-benzonitrileHCID 21976844—
반응물3-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]benzenethiolHCID 21976868—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물4-{[2-(3-Hydroxy-phenylsulfanyl)-ethyl]-[1,2,4]triazol-4-yl-amino}-benzonitrileHCID 21976910—

반응 단계

A mixture of 4-[(2-Bromo-ethyl)-[1,2,4]triazol-4-yl-amino]-benzonitrile (CAB02148=CAB03031, 146 mg, 0.50 mmol), 3-(tert-butyl-dimethylsiloxy)-thiophenol (240 mg, 1.0 mmol) and potassium carbonate (276 mg, 2.0 mmol) in DMF (10 ml) was stirred for 48 hours at room temperature. The mixture was transferred into a separation funnel and ethyl acetate (50 ml) and water (50 ml) were added. The organic layer was separated, washed with brine (30 ml), dried over sodium sulphate and concentrated under reduced pressure. The residue was crystallised from methanol. Yield: 93 mg (55%) colourless crystals (STX512). 1H-NMR (400 MHz, d6-DMSO) δ=3.14 (t, J=7.0 Hz, 2H), 4.02 (t, J=7.0 Hz, 2H), 6.53 (d, J=9.0 Hz, 2H), 6.62 (ddd, J=7.8, 2.0, 0.8 Hz, 1H), 6.70-6.72 (m, 2H), 7.10 (dd, J=7.8, 7.8, 1H), 7.70 (d, J=9.0 Hz, 2H), 8.94 (s, 2H), 9.60 (s, 1H, —OH). 13C-NMR (100 MHz, d6-DMSO) δ=29.53 52.46, 102.38, 112.86, 113.57, 115.36, 119.00, 130.11, 133.94, 135.82, 143.50, 150.71, 157.90, 169.59. LRMS (FAB+): 338.2 (100, [M+H]+). C17H15N5OS (337.4) Calculated: C, 60.52% H, 4.48% N, 20.76%, Found: C, 60.6% H, 4.53% N, 20.8%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08148415B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-5276d23471da4115844b9054ec50d83e
출처 메모uspto-grants-2012_04