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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1402832생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1402832

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참여 물질

역할이름HCID투입량
반응물5-chloro-2-(chloromethyl)-1H-1,3-benzodiazoleHCID 271286—
반응물Glycine, N-(4-chlorophenyl)-, ethyl esterHCID 302644—
반응물Sodium BicarbonateHCID 516892—
용매DimethylformamideHCID 6228—
생성물Ethyl n-[(5-chloro-2-benzimidazolyl)methyl]-n-(4-chlorophenyl)glycinateHCID 6675958222.6%

반응 조건

온도150 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08912186B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-9831c1577fc64d46b7bb4e74cd716567
출처 메모uspto-grants-2014_12