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HRID 37862作成日:2026年10月24日

Cesium carbonate → 1-(4,6-Dimethyl-pyridin-2-yl)-4-(2-methyl-4-nitro-phenyl)-piperazine

https://huagongshe.com/ja/reaction/37862

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物Benzene, 1-chloro-2-methyl-4-nitro-HCID 83315—
反応物1-(4,6-Dimethylpyridin-2-YL)piperazineHCID 23368063—
触媒palladium(II) acetateHCID 167845—
溶媒TolueneHCID 1140—
生成物1-(4,6-Dimethyl-pyridin-2-yl)-4-(2-methyl-4-nitro-phenyl)-piperazineHCID 6685152427.1%

反応手順

Caesium carbonate (10.19 g, 31.38 mmol), 1-chloro-2-methyl-4-nitro-benzene (0.98 g, 5.75 mmol) and 1-(4,6-dimethyl-pyridin-2-yl)-piperazine (1.0 g, 5.23 mmol) were taken in toluene (35 mL) and degassed with argon for 15 min. A slurry of 2-dicyclophosphino-2′-(N,N-dimethylamino)-biphenyl (0.2 g, 0.52 mmol) and palladium acetate (0.116 g, 0.52 mmol) in toluene (5 mL) was added, the mixture degassed for another 10 min and then heated at reflux for 16 h. The mixture was cooled to room temperature and filtered, washing with ethyl acetate. The filtrate was washed with 2N hydrochloric acid, water, and brine, dried over anhydrous sodium sulfate, filtered and concentrated under vacuum to obtain the crude compound. Purification by column chromatography over silica gel (100-200 mesh) using 0-12% ethyl acetate in petroleum ether as eluent gave 1-(4,6-dimethyl-pyridin-2-yl)-4-(2-methyl-4-nitro-phenyl)-piperazine (0.463 g, 27%) as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524705B2
出典データセットuspto-grants-2013_09
ORD IDord-1dcc0993a9df45538c543723262d88fe
出典メモuspto-grants-2013_09