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【结 构 式】

【分子编号】24182

【品名】1-[(2R)-2-amino-5,8-dimethoxy-1,2,3,4-tetrahydro-2-naphthalenyl]-1-ethanone

【CA登记号】

【 分 子 式 】C14H19NO3

【 分 子 量 】249.3098

【元素组成】C 67.45% H 7.68% N 5.62% O 19.25%

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:(V)

Synthesis of intermediate (VI): 1) The reaction of 5,8-dimethoxy-2-tetralone (I) with KCN and ammonium carbonate in refluxing ethanol gives 2-amino-5,8-dimethoxy-1,2,3,4-tetrahydro-2-naphthoic acid (II), which is esterified with methanol-HCl to the corresponding methyl ester (III). The optical resolution of (III) with D-(-)-mandelic acid affords the 2R isomer (IV), which by reaction first with NaH and DMSO and then with Zn and NaOH in water gives (R)-2-acetyl-2-amino-5,8-dimethoxy-1,2,3,4-tetrahydronaphthalene (V). The acetylation of (V) with acetic anhydride in pyridine yields (R)-2-acetyl-2-acetamido-5,8-dimethoxy-1,2,3,4-tetrahydronaphthalene (VI).

1 Ishizumi, K.; Ohashi, N.; Tanno, N.; Sato, H.; Fukui, M.; Morisada, S. (Sumitomo Pharmaceuticals Co., Ltd.); Aminonaphthacene derivs.. EP 0107486; US 4673668 .
2 Ishizumi, K.; et al.; Stereospecific total synthesis of 9-aminoanthracyclines: (+)-9-Amino-9-deoxydaunomycin and related compounds. J Org Chem 1987, 52, 20, 4477-85.
3 Hoshi, A.; Prous, J.; Castaner, J.; SM-5887. Drugs Fut 1988, 13, 11, 962.
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) 24172 5,8-dimethoxy-3,4-dihydro-2(1H)-naphthalenone C12H14O3 详情 详情
(II) 24173 2-amino-5,8-dimethoxy-1,2,3,4-tetrahydro-2-naphthalenecarboxylic acid C13H17NO4 详情 详情
(III) 24180 methyl 2-amino-5,8-dimethoxy-1,2,3,4-tetrahydro-2-naphthalenecarboxylate C14H19NO4 详情 详情
(IV) 24181 methyl (2R)-2-amino-5,8-dimethoxy-1,2,3,4-tetrahydro-2-naphthalenecarboxylate C14H19NO4 详情 详情
(V) 24182 1-[(2R)-2-amino-5,8-dimethoxy-1,2,3,4-tetrahydro-2-naphthalenyl]-1-ethanone C14H19NO3 详情 详情
(VI) 24175 N-[(2R)-2-acetyl-5,8-dimethoxy-1,2,3,4-tetrahydro-2-naphthalenyl]acetamide C16H21NO4 详情 详情
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