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HRID 2116421作成日:2026年10月24日

Hydrochloric Acid → 2-(2-Methyl-5-nitroimidazolyl)ethyl-z,z-octadeca-9,12-dienoate

https://huagongshe.com/ja/reaction/2116421

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物MetronidazoleHCID 4173—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物Linoleic AcidHCID 5280450—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物2-(2-Methyl-5-nitroimidazolyl)ethyl-z,z-octadeca-9,12-dienoateHCID 136388346—

反応手順

To a suspension of metronidazole (1.9 g) in dry dichloromethane (20 ml) was added successively 4-(N,N-dimethylamino)pyridine (1.22 g), 1,3-dicyclohexylcarbodiimide (2.2 g) and linoleic acid (2.8 g). The mixture was stirred at room temperature overnight. To the reaction was added 2M hydrochloric acid (20 ml) and stirring was continued. After filtration the organic layer was separated, washed with 50% saturated brine and finally with saturated aqueous sodium bicarbonate. The dichloromethane solution was dried (sodium sulfate) and evaporated in vacuo (30° C./20 mm Hg). To the resulting residue was added petrol (bp 30-60° C., 20 ml) and the mixture allowed to stand at room temperature for 2 hours, causing the precipitation of the remaining urea. This was removed by filtration and the filtrate was applied to a dry column giving 2-(2-methyl-5-nitroimidazolyl)ethyl-z,z-octadeca-9,12-dienoate as a pale yellow, non distillable oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号USRE040546E1
出典データセットuspto-grants-2008_10
ORD IDord-a6db6d5344c242798568dd614a829e3e
出典メモuspto-grants-2008_10