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HRID 338422作成日:2026年10月25日

2-Methyl-2-butene → 6-chloro-5-[4-[2-(methylamino)-2-oxoethoxy]phenyl]-1H-indole-3-carboxylic acid

https://huagongshe.com/reaction/338422

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methyl-2-buteneHCID 10553—
反応物Trisodium PhosphateHCID 24243—
反応物Sodium ChloriteHCID 23668197—
反応物2-[4-(6-chloro-3-formyl-1H-indol-5-yl)phenoxy]-N-methylacetamideHCID 86698756—
溶媒WaterHCID 962—
溶媒Acetonitrile tert-butanolHCID 22050040—
生成物6-chloro-5-[4-[2-(methylamino)-2-oxoethoxy]phenyl]-1H-indole-3-carboxylic acidHCID 8669875747.8%

反応条件

温度0 °C

反応手順

To a mixture of 2-[4-(6-chloro-3-formyl-1H-indol-5-yl)phenoxy]-N-methylacetamide (120 mg, 0.35 mmol) in acetonitrile/t-butanol (4 mL/4 mL) was added 2-methyl-2-butene (4 mL). The reaction mixture was cooled to 0° C. followed by the addition of an aqueous solution of sodium chlorite (630 mg, 7.00 mmol) and sodium phosphate (monobasic and monohydrate, 930 mg, 7.00 mmol) in water (5 mL) dropwise via additional funnel. The ice bath was removed and the reaction was stirred at room temperature overnight. The reaction was quenched with sodium sulfite. The reaction mixture was concentrated under reduced pressure and the resulting residue was purified by pre-HPLC to give the title compound (60 mg, 47% yield) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889730B2
出典データセットuspto-grants-2014_11
ORD IDord-fd1e3ee2efa049398d61fe6aa8126c07
出典メモuspto-grants-2014_11