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【结 构 式】

【分子编号】31694

【品名】(2R)-2-amino-2-[4-(benzyloxy)phenyl]-N-(3,4-dimethoxyphenethyl)ethanamide

【CA登记号】

【 分 子 式 】C25H28N2O4

【 分 子 量 】420.5084

【元素组成】C 71.41% H 6.71% N 6.66% O 15.22%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(XIII)

The formylation of 2-(4-hydroxyphenyl)glycine (IX) as usual gives N-formyl-2-(4-hydroxyphenyl)glycine (X), which by treatment with benzyl alcohol as before yields N-formyl-2-(4-benzyloxyphenyl)glycine (XI). The condensation of (XI) with the amine (IV) by means of butyl chloroformate affords the corresponding amide (XII), which is deformylated by treatment with HCl in methanol to give the glycinamide (XIII). The diazotation of (XIII) with NaNO2 in acetic acid affords N-(3,4-dimethoxyphenylethyl)-O-acetyl-4-benzyloxymandel-amide (XIV), which is finally reduced and deacetylated with LiAlH4 in THF yielding the protected product (VI).

1 Noguchi, K.; Irie, K.; Preparation of optically active benzyl alcohol derivative. JP 54070232 .
2 Noguchi, K.; Irie, K.; Preparation of optically active benzyl alcohol derivative. JP 54070233 .
3 Blancafort, P.; Castaner, J.; Serradell, M.N.; TA-064. Drugs Fut 1982, 7, 6, 407.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(IV) 10098 2-(3,4-Dimethoxyphenyl)-1-ethanamine; 3,4-Dimethoxyphenethylamine; 2-(3,4-Dimethoxyphenyl)ethylamine 120-20-7 C10H15NO2 详情 详情
(VI) 31687 (1R)-1-[4-(benzyloxy)phenyl]-2-[(3,4-dimethoxyphenethyl)amino]-1-ethanol C25H29NO4 详情 详情
(IX) 31690 (2R)-2-amino-2-(4-hydroxyphenyl)ethanoic acid; (2R)-2-(4-hydroxyphenyl)glycine; D-(-)-p-Hydroxyphenylglycine; (R)-2-amino-2-(4-hydroxyphenyl)acetic acid 22818-40-2 C8H9NO3 详情 详情
(X) 31691 (2R)-2-(formylamino)-2-(4-hydroxyphenyl)ethanoic acid C9H9NO4 详情 详情
(XI) 31692 N-formyl-2-(4-benzyloxyphenyl)glycine; (2R)-2-[4-(benzyloxy)phenyl]-2-(formylamino)ethanoic acid C16H15NO4 详情 详情
(XII) 31693 (2R)-2-[4-(benzyloxy)phenyl]-N-(3,4-dimethoxyphenethyl)-2-(formylamino)ethanamide C26H28N2O5 详情 详情
(XIII) 31694 (2R)-2-amino-2-[4-(benzyloxy)phenyl]-N-(3,4-dimethoxyphenethyl)ethanamide C25H28N2O4 详情 详情
(XIV) 31695 (1R)-1-[4-(Benzyloxy)phenyl]-2-[(3,4-dimethoxyphenethyl)amino]-2-oxoethyl acetate; N-(3,4-Dimethoxyphenylethyl)-O-acetyl-4-benzyloxymandel-amide C27H29NO6 详情 详情
Extended Information