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【结 构 式】

【分子编号】34560

【品名】trimethyl(1-propynyl)silane

【CA登记号】6224-91-5

【 分 子 式 】C6H12Si

【 分 子 量 】112.24678

【元素组成】C 64.2% H 10.78% Si 25.02%

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:(IV)

The title compound was prepared by two related ways from 3-iodo-8-methoxy-4-(2-methylphenyl)aminoquinoline (I). Alkylationof (I) with allyl bromide (II) and NaH afforded the N-allyl amine (III). Subsequent intramolecular palladium-catalyzed Heck reaction in (III) produced the title pyrroloquinoline. In an alternative procedure, the intermolecular palladium-catalyzed heteroannulation of (I) with 1-trimethylsilylpropyne (IV) gave the silyl pyrroloquinoline (V), which was finally desilylated by means of trifluoroacetic acid.

1 Yum, E.K.; et al.; Synthesis and pharmacological profile of 1-aryl-3-substituted pyrrolo[3,2-c]quinolones. Bioorg Med Chem Lett 1999, 9, 19, 2819.
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) 34558 3-iodo-8-methoxy-N-(2-methylphenyl)-4-quinolinamine; N-(3-iodo-8-methoxy-4-quinolinyl)-N-(2-methylphenyl)amine C17H15IN2O 详情 详情
(II) 11463 3-Bromo-1-propene; 3-Bromopropene;allyl bromide 106-95-6 C3H5Br 详情 详情
(III) 34559 N-allyl-3-iodo-8-methoxy-N-(2-methylphenyl)-4-quinolinamine; N-allyl-N-(3-iodo-8-methoxy-4-quinolinyl)-N-(2-methylphenyl)amine C20H19IN2O 详情 详情
(IV) 34560 trimethyl(1-propynyl)silane 6224-91-5 C6H12Si 详情 详情
Extended Information