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HRID 16007生成日期:2026年10月23日

三乙胺 → 1-[1-(quinolin-6-ylmethyl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-6-yl]pyrrolidin-3-ol

https://huagongshe.com/zh-CN/reaction/16007

反应方程式

参与物

角色名称HCID投料
反应物三乙胺HCID 8471—
反应物3-羟基吡咯烷HCID 98210—
反应物6-((6-bromo-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinolineHCID 54775608—
溶剂异丙醇HCID 3776—
产物1-[1-(quinolin-6-ylmethyl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-6-yl]pyrrolidin-3-olHCID 5934180099.5%

反应条件

温度70 °C

反应步骤

A mixture of 6-((6-bromo-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinoline (5.00 g, 14.7 mmol), pyrrolidin-3-ol (2.55 g, 29.3 mmol), and triethylamine (4.09 mL, 29.3 mmol) in 2-propanol (32 mL) was heated in the microwave for 30 minutes at 70° C. in two vials. The reaction mixtures were combined and concentrated. The crude product was purified by flash chromatography using a Horizon purification system in three batches (2×40M and 1×40S columns) eluting with chloroform/methanol (0.1-8%). The resulting solid was dissolved in chloroform containing 0.1% methanol (810 mL) and washed with water and 1:1 water:brine, dried (MgSO4), filtered and concentrated to afford 1-[1-(quinolin-6-ylmethyl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-6-yl]pyrrolidin-3-ol (5.08 g, 99%).

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US07732604B2
来源数据集uspto-grants-2010_06
ORD IDord-f089dea19870496996dd805e2acbbcdb
来源说明uspto-grants-2010_06