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【结 构 式】

【分子编号】51846

【品名】 

【CA登记号】

【 分 子 式 】C14H20FeN2

【 分 子 量 】272.17128

【元素组成】C 61.78% H 7.41% Fe 20.52% N 10.29%

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)

The (dimethylaminomethyl)ferrocene (I) was metalated with butyllithium and the organolithium intermediate (II) was condensed with dimethylformamide to furnish, after aqueous quenching, the ferrocenecarboxaldehyde (III). Aldehyde (III) was converted to oxime (IV) by treatment with hydroxylamine in aqueous ethanol. Reduction of oxime (IV) using LiAlH4 produced the primary amine (V). This was then condensed with 4,7-dichloroquinoline (VI) in hot NMP, and the resulting adduct was finally isolated as the L-tartrate salt.

1 Domarle, O.; et al.; In vitro antimalarial activity of a new organometallic analog, ferrocene-chloroquine. Antimicrob Agents Chemother 1998, 42, 3, 540.
2 Biot, C.; et al.; Synthesis an antimalarial activity in vitro and in vivo of a new ferrocene-chloroquine analogue. J Med Chem 1997, 40, 23, 3715.
3 Lebibi, J.; Brocard, J.; Maciejewski, L. (Université des Sciences et Technologies de Lille - Lille 1); Antimalarial organometallic iron complexes. WO 9635698 .
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) 51842   C13H17FeN 详情 详情
(II) 51843   C13H16FeLiN 详情 详情
(III) 51844   C14H17FeNO 详情 详情
(IV) 51845   C14H18FeN2O 详情 详情
(V) 51846   C14H20FeN2 详情 详情
(VI) 38277 4,7-dichloroquinoline 86-98-6 C9H5Cl2N 详情 详情
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