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HRID 859914作成日:2026年10月26日

Triethylamine → Tert-butyl 4-[5-(pyridin-2-ylethynyl)pyridin-2-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/859914

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物EthynylpyridineHCID 137268—
反応物tert-Butyl 4-(5-iodopyridin-2-yl)piperazine-1-carboxylateHCID 7164639—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178418397HCID 178418397—
溶媒DimethylacetamideHCID 31374—
生成物Tert-butyl 4-[5-(pyridin-2-ylethynyl)pyridin-2-yl)piperazine-1-carboxylateHCID 69606771100%

反応手順

To a stirred solution of tert-butyl 4-(5-iodopyridin-2-yl)piperazine-1-carboxylate (4.087 g, 10.5 mmol) in DMA (75 mL) at RT was added 2-ethynylpyridine, (CAS number 1945-84-2, 1.17 mL, 11.5 mmol), triethylamine (4.4 mL, 31.5 mmol), CuI (800 mg, 4.2 mmol) and Pd(PPh3)4 (1.21 g, 1.05 mmol). After stirring for 30 minutes, the DMA was removed in vacuo, and the residue diluted with EtOAc (100 mL). The dark solution was then washed with water (100 mL). The layers were separated and the aqueous phase extracted with EtOAc (3×50 mL). The combined organic extracts were then dried, (MgSO4), filtered and concentrated in vacuo. The residue was then purified by flash chromatography (silica gel, 50% EtOAc in hexanes) to give tert-butyl 4-[5-(pyridin-2-ylethynyl)pyridin-2-yl]piperazine-1-carboxylate as a brown oil (3.8 g, 10.5 mmol, 99%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07153857B2
出典データセットuspto-grants-2006_12
ORD IDord-8c23f6c6d6864917aa051df21d3ae555
出典メモuspto-grants-2006_12