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HRID 218作成日:2026年10月24日

Benzene, 1-bromo-3-methyl-2-nitro- → 4-(3-Methyl-2-nitrophenyl)-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/ja/reaction/218

反応式

関与物質

役割名称HCID仕込み量
反応物Benzene, 1-bromo-3-methyl-2-nitro-HCID 142929—
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
試薬Cesium carbonateHCID 10796—
触媒1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
触媒Palladium (II) acetateHCID 4144353—
溶媒1,4-DioxaneHCID 31275—
生成物4-(3-Methyl-2-nitrophenyl)-piperazine-1-carboxylic acid tert-butyl esterHCID 6010877516.81%

反応条件

温度80 °C

反応手順

tert-butyl piperazine-1-carboxylate (172 mg, 0.93 mmol) and 1-bromo-3-methyl-2-nitrobenzene (0.124 mL, 0.93 mmol), were added to a stirred solution of diacetoxypalladium (20.78 mg, 0.09 mmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (107 mg, 0.19 mmol) and cesium carbonate (664 mg, 2.04 mmol) dissolved in dioxane (3 mL). The resulting solution was stirred at 80 °C under nitrogen overnight. The reaction mixture was filtered, dried under vaccum. The crude product was purified by flash chromatography on silica gel eluting with 5 to 15% ethyl acetate in petroleum ether. The solvent was evaporated to dryness to afford tert-butyl 4-(3-methyl-2-nitrophenyl)piperazine-1-carboxylate (50.0 mg, 16.81 %) as a orange oil.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-100bcab4f1bd45d89d76662307487cf4
出典メモ750 AstraZeneca ELN dataset