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【结 构 式】

【分子编号】39690

【品名】4-(6-bromohexyl)-3,5-heptanedione

【CA登记号】

【 分 子 式 】C13H23BrO2

【 分 子 量 】291.22842

【元素组成】C 53.62% H 7.96% Br 27.44% O 10.99%

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:(VI)

Condensation of the lithium salt of 3,5-heptanedione (V) with 1,6-dibromohexane (II) in DMF giving 4-(6-bromohexyl)-3,5-heptanedione (VI), which is then condensed with 2-chloro-4-methoxyphenol (I) by means of NaH in DMF.

1 Diana, G.D.; et al.; Antiviral acticity of some beta-diketones. 2. Aryloxy alkyl diketones. In vitro activity aganist both RNA and DNA viruses. J Med Chem 1977, 20, 6, 757-761.
2 Hopkins, S.J.; Castaner, J.; Arildone. Drugs Fut 1978, 3, 1, 12.
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) 39686 2-chloro-4-methoxyphenol 18113-03-6 C7H7ClO2 详情 详情
(II) 24786 1,6-dibromohexane 629-03-8 C6H12Br2 详情 详情
(V) 39689 3,5-heptanedione 7424-54-6 C7H12O2 详情 详情
(VI) 39690 4-(6-bromohexyl)-3,5-heptanedione C13H23BrO2 详情 详情
Extended Information