2423-65-6
基本信息
吡嗪-1-氧化物
吡嗪-N-氧化物
PYRAZINE N-OXIDE
RARECHEM BG FB 0041
1-oxidopyrazin-1-ium
Pyrazine N-oxide 97%
物理化学性质
| 熔点 | 112-116 °C |
| 沸点 | 126-127 °C(Press: 14 Torr) |
| 密度 | 1.19±0.1 g/cm3(Predicted) |
| 储存条件 | under inert gas (nitrogen or Argon) at 2-8°C |
| 酸度系数(pKa) | 0.45±0.39(Predicted) |
| 形态 | solid |
| 外观 | Light yellow to yellow Solid |
| InChI | 1S/C4H4N2O/c7-6-3-1-5-2-4-6/h1-4H |
| InChIKey | RUIZBQQGWNBRFH-UHFFFAOYSA-N |
| SMILES | [O-][n+]1ccncc1 |
安全数据
| 危险性符号(GHS) | ![]() ![]() ![]() GHS02,GHS05,GHS07 |
| 警示词 | 危险 |
| 危险性描述 | H228-H302-H315-H318-H335 |
| 防范说明 | P210-P240-P280-P301+P312-P302+P352-P305+P351+P338 |
| 危险品标志 | F,Xn |
| 危险类别码 | 11-22-37/38-41 |
| 安全说明 | 26-39 |
| 危险品运输编号 | UN 1325 4.1/PG 2 |
| WGK Germany | 3 |
| 存储类别 | 4.1B - Flammable solid hazardous materials |
| 危险性类别 | Acute Tox. 4 Oral Eye Dam. 1 Flam. Sol. 1 Skin Irrit. 2 STOT SE 3 |
制备方法
290-37-9
2423-65-6
一般程序1:二嗪氧化;将吡嗪(1当量)和mCPBA(1当量)溶解在DCM(0.2M)中。将反应混合物在室温下搅拌16小时。随后加入PPh3(0.5当量)以淬灭未反应的过酸,继续搅拌4小时。反应完成后,减压浓缩去除溶剂,残余物通过硅胶柱色谱纯化。吡嗪-N-氧化物的合成按照一般程序1进行,使用100% EtOAc作为初始洗脱剂,随后改用20% MeOH/EtOAc混合溶剂进行梯度洗脱,得到白色固体产物,收率88%。产物表征数据如下:1H NMR (300 MHz, CDCl3, 293 K, TMS): δ 8.50 (2H, d, J = 3.9 Hz), 8.14 (2H, d, J = 4.8 Hz); 13C NMR (75 MHz, CDCl3, 293 K, TMS): 147.8, 134.0; HRMS (ESI) m/z calculated for C4H4N2O [M]+: 96.0324, found: 96.0295; 熔点: 103.2-104.5 °C; IR (νmax/cm-1): 3120, 3088, 1595, 861, 847, 838; Rf (20% MeOH/EtOAc): 0.3。
参考文献:
[1] Organic Letters, 2017, vol. 19, # 18, p. 4707 - 4709
[2] Organic Letters, 2018, vol. 20, # 8, p. 2346 - 2350
[3] Angewandte Chemie - International Edition, 2006, vol. 45, # 46, p. 7781 - 7786
[4] Patent: US2008/132698, 2008, A1. Location in patent: Page/Page column 17-18
[5] Chemical Communications, 2015, vol. 51, # 12, p. 2425 - 2428


