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【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.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 18879 3,4-dihydro-1H-1-benzazepine-2,5-dione C10H9NO2 详情 详情
(II) 18880 (E)-1-(3-chlorophenyl)-3-phenyl-2-propen-1-one 20426-48-6 C15H11ClO 详情 详情
(III) 18881 4-[3-(3-chlorophenyl)-3-oxo-1-phenylpropyl]-3,4-dihydro-1H-1-benzazepine-2,5-dione C25H20ClNO3 详情 详情
Extended Information