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HRID 1461439作成日:2026年10月25日

Sodium Bicarbonate → 1-(4-Chlorobenzoyl)-N-hydroxy-5-methoxy-2-methyl-1H-indole-3-methanamine

https://huagongshe.com/reaction/1461439

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium BicarbonateHCID 516892—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-carboxaldehydeHCID 10892787—
溶媒Acetic AcidHCID 176—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物1-(4-Chlorobenzoyl)-N-hydroxy-5-methoxy-2-methyl-1H-indole-3-methanamineHCID 15027390—

反応条件

温度0 °C

反応手順

To a suspension of 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-lH-indole-3-carboxaldehyde, oxime (1.0 g, 2.9 mmol) in 15 ml of acetic acid is added 0.9 g (14.6 mmol) of sodium cyanoborohydride (0.9 g, 14.6 mmol). The reaction mixture is stirred vigorously for three hours whereupon an additional 0.35 g (5.6 mmol) of the reducing agent is added. After an additional 45 minutes the reaction mixture is diluted with ethyl acetate and methylene chloride, cooled to 0° C., and 300 ml of a saturated solution of sodium bicarbonate is added dropwise while continuing to stir vigorously. This mixture is diluted further with 400 ml of ethyl acetate and separated from the aqueous phase (pH=9). The organic phase is washed again with a saturated solution of sodium bicarbonate, water, and finally a saturated solution of sodium chloride. It is dried over magnesium sulfate, filtered, and concentrated to a yellow oil which is crude 1-(4-chlorobenzoyl)-N-hydroxy-5-methoxy-2-methyl-lH-indole-3-methanamine and is used without further purification in the subsequent reaction. Mass balance is quantitative. A sample recrystallized from methylene chloride has a mp of 164°-165° C. (dec).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05075330
出典データセットuspto-grants-1991_12
ORD IDord-fa75919616d44d4e940f5943f0741d6c
出典メモuspto-grants-1991_12