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HRID 1070852作成日:2026年10月26日

Benzyl Bromide → 6-[[2-Benzylmercapto-1-(4-methylphenyl)-1H-benzimidazol-6-yl]oxy]Hexanoic Acid Methyl Ester

https://huagongshe.com/reaction/1070852

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Dicyclohexano-18-crown-6HCID 85955—
反応物Potassium BicarbonateHCID 516893—
反応物HCID 178500330HCID 178500330—
溶媒DimethylformamideHCID 6228—
生成物6-[[2-Benzylmercapto-1-(4-methylphenyl)-1H-benzimidazol-6-yl]oxy]Hexanoic Acid Methyl EsterHCID 10162512—

反応条件

温度20 °C

反応手順

800 mg of 6-[[2-mercapto-1-(4-methylphenyl)-1H-benzimidazol-6-yl]oxy]hexanoic acid methyl ester was dissolved in 8 ml of N,N-dimethylformamide, mixed with 0.3 ml of benzylbromide, 438 mg of potassium hydrogen carbonate and 75 mg of dicyclohexano-18-crown-6, and the mixture was stirred for 15 hours at 20° C. It was filtered, and the filtrate was concentrated by evaporation in a vacuum. The residue was purified by column chromatography on silica gel. 976 mg was obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06903126B2
出典データセットuspto-grants-2005_06
ORD IDord-2118528183b0490796652adc28040645
出典メモuspto-grants-2005_06