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HRID 1886355作成日:2026年10月24日

Imidazole → 5-(1H-imidazol-1-ylmethyl)quinoxaline

https://huagongshe.com/ja/reaction/1886355

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物5-(Bromomethyl)quinoxalineHCID 10149129—
溶媒AcetonitrileHCID 6342—
生成物5-(1H-imidazol-1-ylmethyl)quinoxalineHCID 1987586020.5%

反応手順

A mixture of 15.5 parts of 5-(bromomethyl)quinoxaline, 23.5 parts of 1H-imidazole and 160 parts of acetonitrile was stirred for 1.5 hours at reflux temperature. The reaction mixture was evaporated and the residue was taken up in water. The product was extracted three times with 65 parts of dichloromethane. The combined extracts were dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of dichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from a mixture of 2-propanone and 2,2'-oxybispropane. The product was filtered off and dried, yielding 3 parts (20.5%) of 5-(1H-imidazol-1-ylmethyl)quinoxaline; mp. 121.2° C. (comp. 41).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05151421
出典データセットuspto-grants-1992_09
ORD IDord-fba037ed511e477f91becade0f42eff6
出典メモuspto-grants-1992_09