【结 构 式】 |
【药物名称】ABT-702 【化学名称】5-(3-Bromophenyl)-7-[6-(4-morpholinyl)pyridin-3-yl]pyrido[2,3-d]pyrimidin-4-amine 【CA登记号】214697-26-4 【 分 子 式 】C22H19BrN6O 【 分 子 量 】463.34033 |
【开发单位】Abbott (Originator) 【药理作用】ANALGESIC AND ANESTHETIC DRUGS, Analgesic Drugs, Antiarthritic Drugs, Non-Opioid Analgesics, TREATMENT OF MUSCULOSKELETAL & CONNECTIVE TISSUE DISEASES, Adenosine Kinase Inhibitors |
合成路线1
The condensation between 3-bromobenzaldehyde (I), 1-(6-morpholinyl-3-pyridinyl)ethanone (II) and malononitrile in the presence of ammonium acetate in refluxing benzene produced the bipyridyl derivative (III). Then treatment of (III) with refluxing formamide gave the title pyridopyrimidine.
【1】 Lee, C.-H.; et al.; Discovery of 4-amino-5-(3-bromophenyl)-7-(6-morpholino-pyridin-3-yl) pyrido[2,3-d]pyrimidine, an orally active, non-nucleoside adenosine kinase inhibitor. J Med Chem 2001, 44, 13, 2133. |
【2】 Cowart, M.D.; Lee, C.-H.; Grillot, A.L.; Bhagwat, S.S.; McKie, J. (Abbott Laboratories Inc.); 5,7-Disubstd.-4-aminopyrido[2,3-d]pyrimidine cpds. and their use as adenosine kinase inhibitors. EP 0989986; WO 9846605 . |
【3】 Stewart, A.O.; Perner, R.J.; McKie, J.A.; Zheng, G.Z.; Grillot, A.L.; Cowart, M.D.; Bhagwat, S.S.; Lee, C.-H. (Abbott Laboratories Inc.); 5,7-Disubstd.-4-aminopyrido[2,3-d]pyrimidine cpds.. WO 0023444 . |