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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 886060생성일: 2026년 10월 26일

Potassium Iodide → N,N-diethyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)ethanamine

https://huagongshe.com/reaction/886060

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Sodium hydrideHCID 24758—
반응물2-Bromo-N,N-diethylethanamineHCID 70608—
반응물4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2774010—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물N,N-diethyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)ethanamineHCID 5820467090%

반응 단계

To a solution of 4,4,5,5-tetramethyl-2-(1H-pyrazol-4-yl)-1,3,2-dioxaborolane (250 mg, 1.29 mmol) and sodium hydride (61.8 mg, 2.58 mmol) in tetrahydrofuran at 0° C. was added 2-bromo-N,N-diethylethanamine (558 mg, 2.58 mmol). The reaction was allowed to warm up to room temperature and was monitored by LCMS. After 90 minutes there was still no reaction and potassium iodide (1.71 g, 10.3 mmol) was added and the reaction was heated at 50° C. overnight. The reaction mixture was diluted with a large volume of ethyl acetate and water and partitioned. The organic layer containing the product was washed with brine and concentrated in vacuo to give clear thick oil confirmed by LCMS to be 100% pure N,N-diethyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)ethanamine (340 mg, yield 90%, M+1 294.2)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08242104B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-105e0c6c958e4c40b771dbb9d34b5218
출처 메모uspto-grants-2012_08