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HRID 1436520作成日:2026年10月26日

1,2-Diaminocyclohexane, trans- → 4-[2-(3-Methyl-butyl)-phenyl]-3-oxo-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1436520

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-Diaminocyclohexane, trans-HCID 43806—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物Tert-butyl 3-oxopiperazine-1-carboxylateHCID 3157178—
反応物1-Iodo-2-(3-methyl-butyl)-benzeneHCID 54130445—
触媒Copper iodideHCID 83717—
生成物4-[2-(3-Methyl-butyl)-phenyl]-3-oxo-piperazine-1-carboxylic acid tert-butyl esterHCID 6901761529.2%

反応条件

温度120 °C

反応手順

Charge in a pressure tube copper iodide (16 mg, 0.08 mmol), potassium phosphate (717 g, 3.4 mmol), trans-1,2-diaminocyclohexane (0.020 ml, 0.17 mmol), 1-Iodo-2-(3-methyl-butyl)-benzene (462 mg, 1.7 mmol) and 3-oxo-piperazine-1-carboxylic acid tert-butyl ester (405 g, 2.02 mmol). Purge with nitrogen and add 2 ml of dry 1,4-dioxane. Cap the tube and stir at 120° C. overnight. Filter through celite eluting with EtOAc and concentrate. Purify in a silica gel cartridge (10 g) eluting with hexane followed by EtOAc/hexane 1:1 to give the title compound as a yellow solid (172 mg, 29%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07618978B2
出典データセットuspto-grants-2009_11
ORD IDord-41629d7925de4b56abd75f6a17d7ae1d
出典メモuspto-grants-2009_11