【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