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)quinoline | HCID 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-ol | HCID 59341800 | 99.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 专利号 | US07732604B2 |
|---|
| 来源数据集 | uspto-grants-2010_06 |
|---|
| ORD ID | ord-f089dea19870496996dd805e2acbbcdb |
|---|
| 来源说明 | uspto-grants-2010_06 |
|---|