5-溴吡唑并[1,5-A]嘧啶置于三氯氧磷体系中,化学反应生成5-氯吡唑并[1,5-A]嘧啶 参考文献:Combination Of Kinase Inhibitors And Uses Thereof 标题:Combination Of Kinase Inhibitors And Uses Thereof 摘要:本发明提供了一种治疗与pi3-激酶a和/或受体酪氨酸激酶(rtk)有关的疾病状况的方法.另一方面,该发明提供了一种治疗与pi3-激酶α和/或受体酪氨酸激酶(rtk)有关的疾病状况的方法.另一方面,提出了一种抑制细胞中akt(s473)磷酸化的方法.
专利信息
专利号:US-9676783-B2 优先权日:2008-10-22 标 题:Method of treatment using substituted pyrazolo[1,5-A] pyrimidine compounds 发明人:HAAS JULIA; ANDREWS STEVEN W; JIANG YUTONG; ZHANG GAN 权利人:ARRAY BIOPHARMA INC 摘要:Compounds useful in the synthesis of compounds for treating pain, cancer, inflammation, neurodegenerative disease or Typanosoma cruzi infection in a mammal.
专利号:WO-2024108957-A1 优先权日:2022-11-23 标题 :5-cyanopyrazolo[1,5-a]pyrimidine compound and synthesis method therefor 发明人:MA SHITANG; Qu Hengtong; XU QILIN; SUN CHAOYUE; CHEN NAIDONG 权利人:UNIV WEST ANHUI 摘要:Disclosed is a 5-cyanopyrazolo[1,5-a]pyrimidine compound represented by formula III, wherein R1 is hydrogen, chlorine, bromine, a cyano, a carboxyethoxy, a methyl, an isopropyl, a tert-butyl, a cyclopropyl, an isopropoxy, a phenyl, a 4-fluorophenyl, a 4-chlorophenyl, a 4-methylphenyl, a 4-methoxyphenyl, or a 3-methoxyphenyl, and R2 is a phenyl, a 4-fluorophenyl, a 4-chlorophenyl, a 4-bromophenyl, a 4-methylphenyl, a 4-dimethylaminophenyl, or a furyl. Further disclosed is a method for synthesizing a 5-cyanopyrazolo[1,5-a]pyrimidine compound. The method comprises: mixing a 3-aminopyrazole compound, a cinnamaldehyde derivative, a trimethylsilyl cyanide, a catalyst, a ligand, and a reaction solvent, and reacting same in the presence of oxygen, so as to obtain a 5-cyanopyrazolo[1,5-a]pyrimidine compound.
专利号:DK-2725028-T3 优先权日:2008-10-22 标题:Substituted pyrazolo [1,5-a] pyrimidine compounds as intermediates in the synthesis of kinase inhibitors TRK
专利号:EP-2725028-A1 优先权日:2008-10-22 标题 :Substituted pyrazolo[1,5-]pyrimidine compounds as intermediates in the synthesis of TRK kinase inhibitors
专利号:EP-2725028-B1 优先权日:2008-10-22 标题 :Substituted pyrazolo[1,5-]pyrimidine compounds as intermediates in the synthesis of TRK kinase inhibitors
专利号:HU-E030413-T2 优先权日:2008-10-22 标 题:Substituted pyrazolo[1,5-]pyrimidine compounds as intermediates in the synthesis of TRK kinase inhibitors