29274-28-0

基本信息
4-氯吡唑并[3,4-B]吡啶
4-氯-1H-吡唑并[3,4-B]吡啶
4-氯-1H-吡唑并[3,4-B]吡啶,98%
4-氯-7-氮杂吲唑,4-氯吡唑并[3,4-B]吡啶
7-tetraene
4-CHLORO-7-AZA-1H-INDAZOLE
4-Chloro-1H-pyrazolo[3,4-...
9-triazabicyclo[4.3.0]nona-1
4-Chloro-1H-pyrazolo[3,4-b]pyridine
1H-Pyrazolo[3,4-B]pyridine, 4-chloro-
4-Chloro-1H-pyrazolo[3,4-b]pyridine,98%
3-Chloro-5-hydrazono-penta-1,3-dienylamine
4-CHLORO-1H-PYRAZOLO[3,4-B]PYRIDINE(WXC07940)
物理化学性质
制备方法
![4-氯-1-(4-甲氧基苄基)-1H-吡唑并[3,4-B]吡啶](/CAS/20150408/GIF/924909-17-1.gif)
924909-17-1
![4-氯-1H-吡唑并[3,4-b]吡啶](/CAS/GIF/29274-28-0.gif)
29274-28-0
步骤B:4-氯-1H-吡唑并[3,4-b]吡啶的合成:将4-氯-1-(4-甲氧基苄基)-1H-吡唑并[3,4-b]吡啶(1.506 g,5.502 mmol)溶解于纯三氟乙酸(TFA,8.478 mL,110.0 mmol)中。反应混合物于75℃搅拌2小时。反应完成后,将混合物浓缩至深黄色油状物,加入甲醇(MeOH)诱导白色沉淀形成。过滤收集沉淀,并用甲醇洗涤。滤液中含有目标产物,将其浓缩为黄色油状物,并于真空下干燥过夜,得到黄色蜡状固体。粗产物在乙酸乙酯(EtOAc)和饱和碳酸氢钠(NaHCO3)溶液之间分配。分离有机相和水相,水相用乙酸乙酯(1×)再萃取。合并有机相,用无水硫酸钠(Na2SO4)干燥,过滤后浓缩,得到目标产物4-氯-1H-吡唑并[3,4-b]吡啶(0.845 g,100%收率),为黄色固体。低分辨率质谱(APCI正离子模式)m/e 154, 156(M+,氯同位素模式)。
参考文献:
[1] Patent: US2007/238726, 2007, A1. Location in patent: Page/Page column 99
[2] Patent: WO2009/33084, 2009, A1. Location in patent: Page/Page column 104
[3] Patent: WO2016/4272, 2016, A1. Location in patent: Paragraph 00562
[4] Patent: WO2018/92047, 2018, A1. Location in patent: Page/Page column 112
[5] Patent: WO2014/93383, 2014, A1. Location in patent: Paragraph 00129; 00132