【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% |
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 |