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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 400665생성일: 2026년 10월 24일

6-(5-Chloro-2,3-dihydrobenzofuran-7-yl)-6-methyl-4-trifluoromethylhept-1-yn-4-ol → 2-(1-Benzenesulfonyl-5-bromo-1H-indol-2-ylmethyl)-4-(5-chloro-2,3-dihydrobenzofuran-7-yl)-1,1,1-trifluoro-4-methylpentan-2-ol

https://huagongshe.com/ko/reaction/400665

반응식

참여 물질

역할이름HCID투입량
반응물6-(5-Chloro-2,3-dihydrobenzofuran-7-yl)-6-methyl-4-trifluoromethylhept-1-yn-4-olHCID 46939216—
반응물N-(4-Bromo-2-iodophenyl)benzenesulfonamideHCID 60026307—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매DimethylformamideHCID 6228—
용매TriethylamineHCID 8471—
용매Ammonium ChlorideHCID 25517—
생성물2-(1-Benzenesulfonyl-5-bromo-1H-indol-2-ylmethyl)-4-(5-chloro-2,3-dihydrobenzofuran-7-yl)-1,1,1-trifluoro-4-methylpentan-2-olHCID 6002645839.1%

반응 조건

온도70 °C

반응 단계

A mixture of 6-(5-chloro-2,3-dihydrobenzofuran-7-yl)-6-methyl-4-trifluoromethylhept-1-yn-4-ol (170 mg, 0.49 mmol), N-(4-bromo-2-iodophenyl)benzenesulfonamide (220 mg, 0.50 mmol), dichlorobis(triphenylphosphine)palladium (II) (20 mg, 0.03 mmol), and copper (I) iodide (10 mg, 0.05 mmol) in 1 nL of DMF and 0.7 mL of triethylamine was warmed at 70° C. After 45 minutes, the mixture was cooled and diluted with 7 mL of saturated aqueous ammonium chloride solution and extracted with three 7 mL portions of ethyl acetate. The combined organic layers were washed with two 7 mL portions of saturated aqueous ammonium chloride solution, four 7 mL portions of brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The crude residue was purified on silica gel eluting with ethyl acetate-hexanes (0-30% gradient) to afford 126 mg (39% yield) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08741897B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-a35cf86c4af3414da1993fce281260b4
출처 메모uspto-grants-2014_06