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HRID 883952作成日:2026年10月26日

Sodium Acetate → 5-[4-(4-Bromo-phenylcarbamoyl)-2-nitro-phenylsulfanyl]-indole-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/883952

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium AcetateHCID 517045—
反応物N-(4-bromophenyl)-4-chloro-3-nitrobenzamideHCID 1068537—
反応物5-Mercapto-indole-1-carboxylic acid tert-butyl esterHCID 67040248—
溶媒EthanolHCID 702—
生成物5-[4-(4-Bromo-phenylcarbamoyl)-2-nitro-phenylsulfanyl]-indole-1-carboxylic acid tert-butyl esterHCID 6704099685%

反応手順

A solution of the product of Example 59C (39.9 mg, 0.160 mmol) in anhydrous ethanol (2 mL) under a nitrogen atmosphere was treated with the product of Example 49A (56.8 mg, 0.160 mmol) and anhydrous sodium acetate (66 mg, 0.800 mmol) at room temperature, then heated at reflux for 2 hours. The reaction was cooled to room temperature and the solvent removed by rotary evaporation under vacuum. The residue was taken up in ethyl acetate (50 mL) and washed with water (2×25 mL) and brine (25 mL). The organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum. Purification by silica gel flash chromatography using methylene chloride as eluent afforded the title compound as a yellow solid (77 mg, 85%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08236950B2
出典データセットuspto-grants-2012_08
ORD IDord-d69c1fb25acb42a79c1b358340983ce4
出典メモuspto-grants-2012_08