【结 构 式】 |
【药物名称】 【化学名称】2-(3-Chlorophenyl)-4-phenyl-6,7-dihydro-5H-pyrido-[3,2-d][1]benzazepin-6-one 【CA登记号】 【 分 子 式 】C25H17ClN2O 【 分 子 量 】396.88004 |
【开发单位】Univ. Hamburg, Hamburg (DE) 【药理作用】ONCOLYTIC DRUGS, MISCELLANEOUS ANTINEOPLASTIC AGENTS |
合成路线1
Benzazepinedione (I) was condensed with propenone (II) in the presence of a catalytic amount of KOH in ethanol to furnish a diasteromeric mixture of the Michael adducts (III). This mixture was then cyclized and oxidized by means of ammonium ferric sulfate and ammonium acetate in refluxing acetic acid to provide the desired pyridobenzazepinone.
【1】 Link, A.; Kunick, C.; d-Fused[1]benzazepines with selective in vitro antitumor activity: Synthesis and structure-activity relationships. J Med Chem 1998, 41, 8, 1299. |
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