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HRID 1507310作成日:2026年10月27日

5-Bromo-1-methyl-1H-imidazole → (1-Methyl-1H-imidazol-5-yl)(3-methyl-4-nitrophenyl)methanone

https://huagongshe.com/reaction/1507310

反応式

関与物質

役割名称HCID仕込み量
反応物5-Bromo-1-methyl-1H-imidazoleHCID 1515258—
反応物N-methoxy-N,3-dimethyl-4-nitrobenzamideHCID 46318653—
反応物HCID 178461630HCID 178461630—
溶媒DichloromethaneHCID 6344—
生成物(1-Methyl-1H-imidazol-5-yl)(3-methyl-4-nitrophenyl)methanoneHCID 86715615—

反応手順

A solution of EtMgBr (3.0 M in diethylether, 8.5 mL, 25.69 mmol) was added dropwise, over a 25 minute period to a solution of 5-bromo-1-methyl-1H-imidazole (4.1 g, 25.69 mmol) in dry DCM (25 mL). The mixture was stirred at room temperature for 15 minutes, cooled in an ice-brine bath and N-methoxy-N,3-dimethyl-4-nitrobenzamide (4.8 g, 21.41 mmol. Intermediate 13: step a) dissolved in 10 mL of DCM was added dropwise. A dark brown solid mass formed. The ice bath was removed and the mixture stirred at room temperature for 48 hours. Water was added to the suspension followed by 6 M aqueous HCl slowly to neutralize the mixture (pH=6-7). More DCM was added and the layers were separated. The organic layer was dried over Na2SO4, filtered and concentrated. Et2O was added, the slurry sonicated, and the precipitates filtered to provide the title compound as a tan solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09221804B2
出典データセットuspto-grants-2015_12
ORD IDord-841b15bbce4941b98c52ed10e7237997
出典メモuspto-grants-2015_12