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HRID 12448作成日:2026年10月24日

1-Isopropylpiperazine → (2-chloro-3-methyl-3H-imidazol-4-yl)-(4-isopropyl-piperazin-1-yl)-methanone

https://huagongshe.com/ja/reaction/12448

反応式

関与物質

役割名称HCID仕込み量
反応物1-IsopropylpiperazineHCID 78013—
反応物1H-Imidazolium, 2-chloro-4,5-dihydro-1,3-dimethyl-, chlorideHCID 10986715—
反応物2-Chloro-1-methyl-1H-imidazole-5-carboxylic acidHCID 53424429—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
溶媒DiisopropylethylamineHCID 81531—
生成物(2-chloro-3-methyl-3H-imidazol-4-yl)-(4-isopropyl-piperazin-1-yl)-methanoneHCID 59338485—

反応手順

Under nitrogen, 2-chloro-3-methyl-3H-imidazole-4-carboxylic acid (0.161 g, 1.0 mmol) is dissolved in toluene (5 mL, anhydrous) and DIEA (0.26 mL). N-isopropylpiperazine (0.2 M in toluene; 5.5 mL; 1.1 mmol) is added followed by the slow addition of 2-chloro-1,3-dimethylimidazolinium chloride (0.3 M in acetonitrile; 4.0 mL; 1.2 mmol). The reaction mixture is stirred at rt for 2 hr and is then diluted with EtOAc and washed with NaOH (1 N). The aqueous layer is drained and reextracted with EtOAc and the combined organic extracts are extracted twice with HCl (1 N). The combined acidic aqueous extracts are washed with EtOAc then basified with NaOH (2.5 M). The resulting basic aqueous solution is extracted three times with EtOAc and the combined organic extracts are washed with brine, then dried over Na2SO4, filtered and concentrated in vacuo.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728009B1
出典データセットuspto-grants-2010_06
ORD IDord-1c2f61fb48db41e3902576a0f542c4cc
出典メモuspto-grants-2010_06