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【结 构 式】

【分子编号】53949

【品名】methyl 8-anilino-8-oxooctanoate

【CA登记号】

【 分 子 式 】C15H21NO3

【 分 子 量 】263.33668

【元素组成】C 68.42% H 8.04% N 5.32% O 18.23%

与该中间体有关的原料药合成路线共 2 条

合成路线1

该中间体在本合成路线中的序号:(XIII)

5. The condensation of diacid (XII) with aniline (II) by heating at 190 C gives the monoamide (VII), which is esterified by means of Dowex 50W-X2 in refluxing methanol to yield the monoamide monoester (XIII). Finally, this compound is treated with hydroxylamine and NaOMe in methanol to afford the target hydroxamic acid with overall yields of around 37%.

1 Stowell, J.C.; et al.; The synthesis of N-hydroxy-N'-phenyloctanediamide and its inhibitory effect on proliferation of AXC rat prostate cancer cells. J Med Chem 1995, 38, 8, 1411.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(II) 12294 Aniline; Phenylamine 62-53-3 C6H7N 详情 详情
(VII) 53946 8-anilino-8-oxooctanoic acid C14H19NO3 详情 详情
(XII) 11820 Suberic acid; Cork acid; Octanedioic acid 505-48-6 C8H14O4 详情 详情
(XIII) 53949 methyl 8-anilino-8-oxooctanoate C15H21NO3 详情 详情

合成路线2

该中间体在本合成路线中的序号:(II)

 

1 Gediya LK, Chopra P, Purushottamachar P. et al. 2005. A new simple and high-yield synthesis of sub roykuiilide hydroxamic acid and its inhibitory effect alone or in combination with retinoids on proliferation of human prostate cancer cells. J Med Chem, 48 (15): 5047~5051
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) 66965 8-methoxy-8-oxooctanoic acid 3946-32-5 C9H16O4 详情 详情
(II) 53949 methyl 8-anilino-8-oxooctanoate C15H21NO3 详情 详情
Extended Information