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【结 构 式】

【药物名称】Methoctramine

【化学名称】N,N'-Bis[6-[(2-methoxybenzyl)amino]hexyl]-1,8-octanediamine tetrahydrochloride

【CA登记号】104807-46-7

【 分 子 式 】C36H66Cl4N4O2

【 分 子 量 】728.76502

【开发单位】Università degli Studi di Bologna (Originator), Università degli Studi di Camerino (Originator)

【药理作用】Antiarrhythmic Drugs, CARDIOVASCULAR DRUGS, PHARMACOLOGICAL TOOLS

合成路线1

N-(Benzyloxycarbonyl)-6-aminocaproic acid (I) is reacted with 1,8-octanediamine (II) to give amide (III). The protecting group can be removed either by hydrogenolysis or by gaseous HBr affording (IV), which is reduced with borane-methyl sulfide complex to yield N,N'-bis(6-aminohexyl)-1,8-octanediamine (V). Condensation of (V) with 2-methoxybenzaldehyde and subsequent reduction of the intermediate Schiff base gives methoctramine. However, methoctramine can be prepared more conveniently by transforming (IV) to (VI) followed by reduction of amide groups with borane.

1 Melchiorre, C.; Minarini, A.; Quaglia, W.; Tumiatti, V.; METHOCTRAMINE. Drugs Fut 1989, 14, 7, 628.
2 Quaglia, W.; Melchiorre, C.; Cassinelli, A.; Differential blockade of muscarinic receptor subtypes by polymethylene tetraamines. Novel class of selective antagonists of cardiac M2 muscarinic receptors. J Med Chem 1987, 30, 1, 201.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
12568 2-Methoxybenzaldehyde; o-Methoxybenzaldehyde 135-02-4 C8H8O2 详情 详情
(I) 20964 6-[[(benzyloxy)carbonyl]amino]hexanoic acid 1947-00-8 C14H19NO4 详情 详情
(II) 20965 1,8-octanediamine; 8-aminooctylamine 373-44-4 C8H20N2 详情 详情
(III) 20966 benzyl 6,17,24-trioxo-26-phenyl-25-oxa-7,16,23-triazahexacos-1-ylcarbamate C36H54N4O6 详情 详情
(IV) 20967 6-amino-N-[8-[(6-aminohexanoyl)amino]octyl]hexanamide C20H42N4O2 详情 详情
(V) 20968 N(1),N(8)-bis(6-aminohexyl)-1,8-octanediamine; N-(6-aminohexyl)-N-[8-[(6-aminohexyl)amino]octyl]amine C20H46N4 详情 详情
(VI) 20969 6-[(2-methoxybenzyl)amino]-N-[8-([6-[(2-methoxybenzyl)amino]hexanoyl]amino)octyl]hexanamide C36H58N4O4 详情 详情
Extended Information