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HRID 1005503作成日:2026年10月26日

Toluene → 5-(3,5-Dimethylphenylthio)-4-isopropyl-1-[2-(1-methoxycyclopentyloxy)ethoxymethyl]-2-methyl-1H-imidazole

https://huagongshe.com/reaction/1005503

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物2-[5-(3,5-Dimethyl-phenylsulfanyl)-4-isopropyl-2-methyl-imidazol-1-ylmethoxy]-ethanolHCID 478180—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
反応物1,1-Dimethoxy-cyclopentaneHCID 523052—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物5-(3,5-Dimethylphenylthio)-4-isopropyl-1-[2-(1-methoxycyclopentyloxy)ethoxymethyl]-2-methyl-1H-imidazoleHCID 1588718473.2%

反応手順

A solution of 5-(3,5-dimethylphenylthio)-4-isopropyl-1-(2-hydroxyethoxymethyl)-2-methyl-1H-imidazole (1) (301 mg, 0.9 mmol) prepared in accordance with the method as described in WO 96/10019 and p-toluenesulfonic acid hydrate (180 mg, 0.945 mmol) in a mixture of methylene chloride (5 mL) - toluene (1 mL) was concentrated under reduced pressure. The obtained residue was dissolved in methylene chloride (9 mL), to which was added 1,1-dimethoxycyclopentane (1.17 g, 9.00 mmol), and the mixture was stirred for 3 hours. Triethylamine (0.19 mL) was added to the reaction mixture, and the mixture was concentrated under reduced pressure. The residue was purified by chromatography on an alumina column (eluate: hexane - ethyl acetate (2:1)) to give the compound 2 (285 mg, 73 %) as oil. Rf 0.45 (Al2O3 60, Type E, 2:1 hexane -EtOAc).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06054591
出典データセットuspto-grants-2000_04
ORD IDord-1f6688f008bf4fcc9f79d4cef457f625
出典メモuspto-grants-2000_04