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【结 构 式】 
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【分子编号】25762 【品名】3-(bromomethyl)pyrido[3,2-g]quinoline-5,10-dione 【CA登记号】 |
【 分 子 式 】C13H7BrN2O2 【 分 子 量 】303.11486 【元素组成】C 51.51% H 2.33% Br 26.36% N 9.24% O 10.56% |
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 hetero Diels-Alder condensation of quinolinedione (I) with the azabutadiene (II) in the presence of ZnBr2 produced regioselectively the pyridoquinoline (III). Benzylic bromination of (III) using N-bromosuccinimide then gave bromomethyl derivative (IV). Subsequent treatment of (IV) with NaOAc in DMF, followed by hydrolysis of the resulting acetate (V), afforded 3-(hydroxymethyl)pyridoquinoline (VI). This was finally treated with isopropyl isocyanate in the presence of Et3N and dibutyltin diacetate to yield the target carbamate.
| 【1】 Lee, H.; Lee, S.I.; Yang, S.I.; Synthesis and in vitro cytotoxicity of 3-substituted-1,8-diazaanthraquinones produced by Lewis-acid catalyzed hetero Diels-Alder reaction. Bioorg Med Chem Lett 1998, 8, 21, 2991. |
| 中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
|---|---|---|---|---|---|---|
| 30690 | isopropyl isocyanate; 2-isocyanatopropane | 1795-48-8 | C4H7NO | 详情 | 详情 | |
| (I) | 25759 | 5,8-quinolinedione | C9H5NO2 | 详情 | 详情 | |
| (II) | 25760 | 2-methylacrylaldehyde N,N-dimethylhydrazone | C6H12N2 | 详情 | 详情 | |
| (III) | 25761 | 3-methylpyrido[3,2-g]quinoline-5,10-dione | C13H8N2O2 | 详情 | 详情 | |
| (IV) | 25762 | 3-(bromomethyl)pyrido[3,2-g]quinoline-5,10-dione | C13H7BrN2O2 | 详情 | 详情 | |
| (V) | 25763 | (5,10-dioxo-5,10-dihydropyrido[3,2-g]quinolin-3-yl)methyl acetate | C15H10N2O4 | 详情 | 详情 | |
| (VI) | 25764 | 3-(hydroxymethyl)pyrido[3,2-g]quinoline-5,10-dione | C13H8N2O3 | 详情 | 详情 |
Extended Information