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HRID 390323作成日:2026年10月25日

3-Iodothiophene → Butyl 4-(3-thienyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/390323

反応式

関与物質

役割名称HCID仕込み量
反応物3-IodothiopheneHCID 66332—
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
反応物2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
反応物Sodium t-butoxideHCID 23676156—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物Butyl 4-(3-thienyl)piperazine-1-carboxylateHCID 86672487—

反応条件

温度100 °C

反応手順

To a solution of tert-butyl piperazine-1-carboxylate (0.300 g, 1.61 mmol) in 10 mL of toluene under an atmosphere of nitrogen was added 3-iodothiophene (0.390 g, 1.86 mmol), sodium tert-butoxide (0.310 g, 3.22 mmol), tris (dibenzylidenacetone)palladium (0) (0.295 g, 0.322 mmol), and 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (X-Phos, 0.307 g, 0.644 mmol). The mixture was heated to 100° C. for 18 h, cooled to rt, and treated with water. The solution was extracted 3× with ethyl acetate, and the combined organic solution was washed with brine, dried over sodium sulfate, filtered, and concentrated in vacuo. The resultant residue was purified via silica gel chromatography, eluting with 0-70% ethyl acetate, to provide text-butyl 4-(3-thienyl)piperazine-1-carboxylate that gave a proton NMR spectra consistent with theory.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08383638B2
出典データセットuspto-grants-2013_02
ORD IDord-614555e96b724d83b2a7fb7b81e7bf0b
出典メモuspto-grants-2013_02