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HRID 1861048作成日:2026年10月25日

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

https://huagongshe.com/reaction/1861048

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Potassium CarbonateHCID 11430—
反応物6-iodo-1-(2,4,6-trimethyl-benzenesulfonyl)-1H-indazoleHCID 21877396—
反応物HCID 21877521HCID 21877521—
触媒HCID 178418476HCID 178418476—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物6-(3-methoxy-4-methoxymethoxy-phenyl)-1-(2,4,6-trimethyl-benzenesulfonyl)-1H-indazoleHCID 21877354—

反応条件

温度90 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06531491B1
出典データセットuspto-grants-2003_03
ORD IDord-2cfaeafbc4ce4e6dbe5a928592b2a42b
出典メモuspto-grants-2003_03