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【结 构 式】

【药物名称】ADAM-II

【化学名称】6,6-Bis[3-chloro-4-methoxy-5-(methoxycarbonyl)phenyl]-5-hexenoic acid methyl ester

【CA登记号】

【 分 子 式 】C25H26Cl2O8

【 分 子 量 】525.38717

【开发单位】National Cancer Institute (Originator), Purdue University (Originator)

【药理作用】AIDS Medicines, Anti-HIV Agents, ANTIINFECTIVE THERAPY, Reverse Transcriptase Inhibitors

合成路线1

Title compound was prepared by Wittig condensation of benzophenone (I) with the phosphorane derived from (4-methoxycarbonylbutyl)triphenyl phosphonium bromide (II) and sodium hexamethyldisilazide at -78 C.

1 Hejchman, E.; Casimiro-Garcia, A.; Cushman, M.; et al.; New alkenyldiarylmethanes with enhanced potencies as anti-HIV agents which act as non-nucleoside reverse transcriptase inhibitors. J Med Chem 1998, 41, 12, 2076.
2 Rice, W.G.; Casimiro-Garcia, A.; Cushman, M.S. (Purdue Research Foundation; US Department of Health & Human Services); Alkenyldiarylmethane non-nucleoside HIV-1 reverse transcriptase inhibitors. WO 9936384 .
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) 26176 methyl 3-chloro-5-[3-chloro-4-methoxy-5-(methoxycarbonyl)benzoyl]-2-methoxybenzoate C19H16Cl2O7 详情 详情
(II) 26177 (5-methoxy-5-oxopentyl)(triphenyl)phosphonium bromide C24H26BrO2P 详情 详情
Extended Information