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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19906생성일: 2026년 10월 24일

Potassium Carbonate → 4-{[4-(4-Hydroxy-phenylsulfanyl)-butyl]-[1,2,4]triazol-4-yl-amino}-benzonitrile

https://huagongshe.com/ko/reaction/19906

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물4-MercaptophenolHCID 240147—
반응물4-[(2-Bromo-butyl)-[1,2,4]triazol-4-yl-amino]-benzonitrileHCID 21976851—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물4-{[4-(4-Hydroxy-phenylsulfanyl)-butyl]-[1,2,4]triazol-4-yl-amino}-benzonitrileHCID 21976857—

반응 단계

Potassium carbonate (500 mg) was added to a solution of 4-[(2-bromo-butyl)-[1,2,4]triazol-4-yl-amino]-benzonitrile (CAB03001, 384 mg, 1.2 mmol) and 4-hydroxythiophenol (227 mg, 1.8 mmol) in DMF (20 mL). The mixture was stiffed for 18 hours at r.t., diluted with ethyl acetate (100 mL) and extracted with water (two times 30 mL) and brine (30 mL). The organic layer was dried over sodium sulphate and concentrated under reduced pressure. The residue was purified by column chromatography (eluent: ethyl acetate, Rf: 0.30). The resulting oil was dissolved in a small amount of ethyl acetate and the product was precipitated by addition of hexane. Yield: 289 mg (66%). 1H-NMR (400 MHz, d6-DMSO) δ=1.48-1.64 (m, 4H) 2.81 (t, J=6.6 Hz, 2H), 3.81 (t, J=6.8 Hz, 2H), 6.62 (d, J=9.0 Hz, 2H), 6.72 (d, J=8.6 Hz, 2H), 7.19 (d, J=9.0 Hz, 2H), 7.72 (d, J=9.0, 2H), 8.94 (s, 2H), 9.56 (s, 1H, —OH). LRMS (FAB+): 366.1 (100, [M+H]+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745472B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-4bebb1482b4e44bf8af570d5cc5190fb
출처 메모uspto-grants-2010_06