関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 5-Bromo-1-methyl-1H-imidazole | HCID 1515258 | — |
| 反応物 | N-methoxy-N-methyl-4-nitrobenzamide | HCID 2991007 | — |
| 反応物 | HCID 178418443 | HCID 178418443 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (1-Methyl-1H-imidazol-5-yl)(4-nitrophenyl)methanone | HCID 86715600 | — |
反応手順
To a solution of 5-bromo-1-methyl-1H-imidazole (3.22 g, 19.98 mmol) in DCM (15 mL) was added ethyl magnesium bromide (6.66 mL, 19.98 mmol, 3.0 M in diethyl ether) dropwise over a 10 minute period. The resulting orange-red solution was stirred at room temperature for 15 minutes, cooled in an ice bath to 0° C. and N-methoxy-N-methyl-4-nitrobenzamide (3.5 g, 16.65 mmol, Intermediate 7: step a) dissolved in DCM (10 mL) was added dropwise. The ice bath was removed and the solid suspension stirred at room temperature for 48 hours. Water was added followed by 6 M aqueous HCl to a neutral pH (pH=6-7). The aqueous mixture was extracted with DCM, dried over Na2SO4, filtered and concentrated. Et2O was added and the mixture sonicated. The precipitate was collected by filtration and dried to provide the title compound as a tan solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09346782B2 |
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| 出典データセット | uspto-grants-2016_05 |
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| ORD ID | ord-b41eba38d3cc48979088abf09e668c45 |
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| 出典メモ | uspto-grants-2016_05 |
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