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【结 构 式】

【分子编号】63327

【品名】4-chloro-6-nitroquinazoline

【CA登记号】

【 分 子 式 】C8H4ClN3O2

【 分 子 量 】209.59148

【元素组成】C 45.85% H 1.92% Cl 16.92% N 20.05% O 15.27%

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:(II)

Chlorination of 6-nitro-4-quinazolone (I) in refluxing SOCl2 affords 4-chloro-6-nitroquinazoline (II), which is then condensed with 4-phenoxyphenethylamine (III) to furnish the 4-aminoquinazoline (IV). Finally, nitro group reduction employing iron powder and acetic acid gives rise to the title compound.

1 Tobe, M.; Isobe, Y.; Tomizawa, H.; Nagasaki, T.; Takahashi, H.; Fukazawa, T.; Hayashi, H.; Discovery of quinazolines as a novel structural class of potent inhibitors of NF-kappaB activation. Bioorg Med Chem 2003, 11, 3, 383.
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) 34444 6-nitro-4(3H)-quinazolinone C8H5N3O3 详情 详情
(II) 63327 4-chloro-6-nitroquinazoline C8H4ClN3O2 详情 详情
(III) 63328 2-(4-phenoxyphenyl)-1-ethanamine; 4-phenoxyphenethylamine C14H15NO 详情 详情
(IV) 63329 6-nitro-N-(4-phenoxyphenethyl)-4-quinazolinamine; N-(6-nitro-4-quinazolinyl)-N-(4-phenoxyphenethyl)amine C22H18N4O3 详情 详情
Extended Information