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【结 构 式】

【分子编号】51235

【品名】4-chloro-6-[(E)-3-methyl-1-triazenyl]quinazoline

【CA登记号】

【 分 子 式 】C9H8ClN5

【 分 子 量 】221.64892

【元素组成】C 48.77% H 3.64% Cl 15.99% N 31.6%

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)

Arylamine (I) is converted into the corresponding methyltriazene (II) by formation of the corresponding diazonium salt with NaNO2 in HCl/H2O, followed by reaction with methylamine. Finally, the target compound is obtained by coupling of (II) with the corresponding amine in refluxing isopropanol.

1 Vaughan, K.; et al.; Studies of the model of action of antitumor triazenes and triazines. 6. 1-Ayl-3-(hydroxymethyl)-3-methyltriazenes: Synthesis, chemistry, and antitumor properties. J Med Chem 1984, 27, 3, 357.
2 Rewcastle, G.W.; et al.; Tyrosine kinase inhibitors. 5. Synthesis and structure-activity relationships for 4-[(phenylmethyl)amino]- and 4-(phenylamino)quinazolines as potent adenosine 5'-triphosphate binding site inhibitors of the tyrosine kinase domain of the epidermal growth f. J Med Chem 1995, 38, 18, 3482.
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) 51234 4-chloro-6-quinazolinylamine; 4-chloro-6-quinazolinamine C8H6ClN3 详情 详情
(II) 51235 4-chloro-6-[(E)-3-methyl-1-triazenyl]quinazoline C9H8ClN5 详情 详情
(III) 30687 3-methylphenylamine; m-toluidine 108-44-1 C7H9N 详情 详情
Extended Information