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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 859914생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/859914

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물EthynylpyridineHCID 137268—
반응물tert-Butyl 4-(5-iodopyridin-2-yl)piperazine-1-carboxylateHCID 7164639—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418397HCID 178418397—
용매DimethylacetamideHCID 31374—
생성물Tert-butyl 4-[5-(pyridin-2-ylethynyl)pyridin-2-yl)piperazine-1-carboxylateHCID 69606771100%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07153857B2
출처 데이터셋uspto-grants-2006_12
ORD IDord-8c23f6c6d6864917aa051df21d3ae555
출처 메모uspto-grants-2006_12