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【结 构 式】

【药物名称】Bifemelane Hydrochloride, BFM-2703, E-0687, MCI-2016, Celeport, Alnert

【化学名称】N-Methyl-4-[2-(phenylmethyl)phenoxy]-1-butanamine hydrochloride
      2-(4-Methylaminobutoxy)diphenylmethane hydrochloride

【CA登记号】62232-46-6, 90293-01-9 (free base)

【 分 子 式 】C18H24ClNO

【 分 子 量 】305.85108

【开发单位】Eisai (Originator), Mitsubishi Chemical (Originator), Fujisawa (Licensee)

【药理作用】Cognition Disorders, Treatment of, NEUROLOGIC DRUGS

合成路线1

The reaction of 2-hydroxydiphenylmethane (I) with 1,4-dibromobutane (II) in a basic medium affords 2-(4-bromobutoxy)diphenylmethane (III), which is then condensed with methylamine in water - ethanol at room temperature.

1 Kikumoto, R.; et al.; Pharmaceutically active 2-omega-aminoalkoxydiphenylmethanes. US 4091114 .
2 Kikumoto, R.; et al.; 2-Substituted-1-(omega-aminoalkoxy)benzenes. DE 2627227; FR 2315913; NL 7606668 .
3 Kikumoto, R.; et al. (Mitsubishi Chemical Corp.); Process for preparation of 2-(omega-aminoalkyloxy)diphenylmethanes. JP 52033658 .
4 Serradell, M.N.; Blancafort, P.; Castaner, J.; MCI-2016. Drugs Fut 1980, 5, 12, 611.
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) 32707 2-benzylphenol 28994-41-4 C13H12O 详情 详情
(II) 11883 1,4-Dibromobutane; 1,4-Butylene bromide 110-52-1 C4H8Br2 详情 详情
(III) 32708 1-benzyl-2-(4-bromobutoxy)benzene; 2-benzylphenyl 4-bromobutyl ether C17H19BrO 详情 详情
Extended Information