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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 5-chloro-2-(chloromethyl)-1H-1,3-benzodiazole | HCID 271286 | — |
| 반응물 | Glycine, N-(4-chlorophenyl)-, ethyl ester | HCID 302644 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Ethyl n-[(5-chloro-2-benzimidazolyl)methyl]-n-(4-chlorophenyl)glycinate | HCID 66759582 | 22.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08912186B2 |
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| 출처 데이터셋 | uspto-grants-2014_12 |
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| ORD ID | ord-9831c1577fc64d46b7bb4e74cd716567 |
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| 출처 메모 | uspto-grants-2014_12 |
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