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【结 构 式】

【分子编号】64845

【品名】4-(6-methoxy-1,3-benzothiazol-2-yl)-N-methylaniline; N-[4-(6-methoxy-1,3-benzothiazol-2-yl)phenyl]-N-methylamine

【CA登记号】

【 分 子 式 】C15H14N2OS

【 分 子 量 】270.35504

【元素组成】C 66.64% H 5.22% N 10.36% O 5.92% S 11.86%

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:(III)

Condensation of 2-amino-5-methoxythiophenol (I) with 4-(methylamino)benzoic acid (II) in hot polyphosphoric acid produces the benzothiazole derivative (III), which is finally submitted to methyl ether cleavage by means of BBr3 to give the target hydroxy compound.

1 Mathis, C.A.; Wang, Y.; Holt, D.P.; Huang, G.-F.; Debnath, M.L.; Klunk, W.E.; Synthesis and evaluation of 11C-labeled 6-substituted 2-arylbenzothiazoles as amyloid imaging agents. J Med Chem 2003, 46, 13, 2740.
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) 25876 2-amino-5-methoxyphenylhydrosulfide; 5-Methoxy-2-aminothiophenol;2-Mercapto-4-methoxyaniline;2-amino-5-methoxybenzenethiol;2-Amino-5-methoxy-1-benzenethiol 6274-29-9 C7H9NOS 详情 详情
(II) 64844 4-(methylamino)benzoic acid C8H9NO2 详情 详情
(III) 64845 4-(6-methoxy-1,3-benzothiazol-2-yl)-N-methylaniline; N-[4-(6-methoxy-1,3-benzothiazol-2-yl)phenyl]-N-methylamine C15H14N2OS 详情 详情
Extended Information