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HRID 1519258作成日:2026年10月25日

2'-Nitro-4-thiocarbamoyl-biphenyl-2-carboxylic acid methyl ester → 4-[4-(4-Fluoro-phenyl)-thiazol-2-yl]-2'-nitro-biphenyl-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1519258

反応式

関与物質

役割名称HCID仕込み量
反応物2'-Nitro-4-thiocarbamoyl-biphenyl-2-carboxylic acid methyl esterHCID 86679832—
反応物4-[4-(4-Fluoro-phenyl)-thiazol-2-yl]-2'-nitro-biphenyl-2-carboxylic acid methyl ester 4-Fluorophenacyl bromideHCID 86679838—
溶媒EthanolHCID 702—
生成物4-[4-(4-Fluoro-phenyl)-thiazol-2-yl]-2'-nitro-biphenyl-2-carboxylic acid methyl esterHCID 8667983757.5%

反応条件

温度45 °C

反応手順

4-[4-(4-Fluoro-phenyl)-thiazol-2-yl]-2′-nitro-biphenyl-2-carboxylic acid methyl ester 4-Fluorophenacyl bromide (available from Alfa Aesar; 35 mg, 0.16 mmol) was added to a suspension of 2′-nitro-4-thiocarbamoyl-biphenyl-2-carboxylic acid methyl ester (which may be prepared as described for Intermediate 4; 50 mg, 0.16 mmol) in ethanol (2 mL) and the resulting mixture was stirred at 45° C. for 20 h. The reaction mixture was concentrated to a small volume and cooled. The precipitate was collected by filtration to give 4-[4-(4-fluoro-phenyl)-thiazol-2-yl]-2′-nitro-biphenyl-2-carboxylic acid methyl ester (40 mg) which was used directly in the next step without purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09073881B2
出典データセットuspto-grants-2015_07
ORD IDord-94e822ac3930439782e9bac5ab1fb868
出典メモuspto-grants-2015_07