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HRID 1402832作成日:2026年10月26日

5-chloro-2-(chloromethyl)-1H-1,3-benzodiazole → Ethyl n-[(5-chloro-2-benzimidazolyl)methyl]-n-(4-chlorophenyl)glycinate

https://huagongshe.com/reaction/1402832

反応式

関与物質

役割名称HCID仕込み量
反応物5-chloro-2-(chloromethyl)-1H-1,3-benzodiazoleHCID 271286—
反応物Glycine, N-(4-chlorophenyl)-, ethyl esterHCID 302644—
反応物Sodium BicarbonateHCID 516892—
溶媒DimethylformamideHCID 6228—
生成物Ethyl n-[(5-chloro-2-benzimidazolyl)methyl]-n-(4-chlorophenyl)glycinateHCID 6675958222.6%

反応条件

温度150 °C

反応手順

The mixture of ethyl N-(4-chlorophenyl)glycinate (0.43 g), 5-chloro-2-chloromethylbenzimidazole (0.4 g), and sodium bicarbonate (0.17 g) in N,N-dimethylformamide (2 ml) was stirred at 150° C. for 0.5 h. After cooling to rt the mixture was poured into saturated sodium bicarbonate solution (50 ml) and extracted twice with EtOAc (40 ml). The combined organic layers were washed with 10% sodium carbonate solution (40 ml) and water (40 ml) and dried (sodium sulfate). After concentration the crude (0.66 g) was purified by flash chromatography (dichloromethane/1% methanol) on silica gel to provide an orange solid. The solid was further purified by trituration with diethyl ether to give ethyl N-[(5-chloro-2-benzimidazolyl)methyl]-N-(4-chlorophenyl)glycinate (0.17 g) as a light orange crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08912186B2
出典データセットuspto-grants-2014_12
ORD IDord-9831c1577fc64d46b7bb4e74cd716567
出典メモuspto-grants-2014_12