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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1861048생성일: 2026년 10월 26일

Triethylamine → 6-(3-methoxy-4-methoxymethoxy-phenyl)-1-(2,4,6-trimethyl-benzenesulfonyl)-1H-indazole

https://huagongshe.com/reaction/1861048

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Potassium CarbonateHCID 11430—
반응물6-iodo-1-(2,4,6-trimethyl-benzenesulfonyl)-1H-indazoleHCID 21877396—
반응물HCID 21877521HCID 21877521—
촉매HCID 178418476HCID 178418476—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물6-(3-methoxy-4-methoxymethoxy-phenyl)-1-(2,4,6-trimethyl-benzenesulfonyl)-1H-indazoleHCID 21877354—

반응 조건

온도90 °C

반응 단계

A mixture of 6-iodo-1-(2,4,6-trimethyl-benzenesulfonyl)-1H-indazole (5.78 g, 13.56 mmol, 1.00 equiv) and 3-methoxy-4-(methoxymethoxy)benzene-boronic acid (3.45 g, 16.27 mmol, 1.20 equiv) under argon was dissolved in dioxane (15 mL) and water (2.0 mL). To this solution was added triethylamine (2.83 mL, 20.3 mmol, 1.5 equiv), potassium carbonate (2.8 g, 20.3 mmol, 1.5 equiv) and dichlorobis(triphenylphosphine)palladium (476 mg, 0.678 mmol, 0.05 equiv). The reaction mixture was heated to 90° C. for 2 h and then was cooled to 23° C. The mixture was separated between ethyl acetate (250 mL) and saturated sodium bicarbonate (150 mL). The organic material was dried over sodium sulfate, decanted and concentrated under reduced pressure to give crude 6-(3-methoxy-4-methoxymethoxy-phenyl)-1-(2,4,6-trimethyl-benzenesulfonyl)-1H-indazole that was dried under high vacuum for 15 h and was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06531491B1
출처 데이터셋uspto-grants-2003_03
ORD IDord-2cfaeafbc4ce4e6dbe5a928592b2a42b
출처 메모uspto-grants-2003_03