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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 5-chloro-2-(chloromethyl)-1H-1,3-benzodiazole | HCID 271286 | — |
| 反応物 | Glycine, N-(4-chlorophenyl)-, ethyl ester | HCID 302644 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Ethyl n-[(5-chloro-2-benzimidazolyl)methyl]-n-(4-chlorophenyl)glycinate | HCID 66759582 | 22.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08912186B2 |
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| 出典データセット | uspto-grants-2014_12 |
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| ORD ID | ord-9831c1577fc64d46b7bb4e74cd716567 |
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| 出典メモ | uspto-grants-2014_12 |
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