【结 构 式】 |
【分子编号】43891 【品名】2-quinolinylmethyl 4-methylbenzenesulfonate 【CA登记号】 |
【 分 子 式 】C17H15NO3S 【 分 子 量 】313.37704 【元素组成】C 65.16% H 4.82% N 4.47% O 15.32% S 10.23% |
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)Synthesis of intermediate 4-(2-quinolinylmethoxy)phenol (V): The oxidation of 2-methylquinoline with urea and H2O2 in dichloromethane gives the N-oxide (II), which is treated with TsCl and K2CO3 in acetonitrile to yield the tosylate (III). Finally this compound is condensed with an excess of hydroquinone by means of NaOH in methanol/acetonitrile to afford the target intermediate (V).
【1】 Sledeski, A.W.; et al.; A convergent synthesis of an LTD4 antagonist, RG12525. Tetrahedron Lett 1997, 38, 7, 1129. |
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) | 13161 | Quinaldine; 2-Methylquinoline | 91-63-4 | C10H9N | 详情 | 详情 |
(II) | 43890 | 2-methyl-1-quinoliniumolate | C10H9NO | 详情 | 详情 | |
(III) | 43891 | 2-quinolinylmethyl 4-methylbenzenesulfonate | C17H15NO3S | 详情 | 详情 | |
(IV) | 13163 | p-Dihydrobenzene; Hydroquinone | 123-31-9 | C6H6O2 | 详情 | 详情 |
(V) | 13164 | 4-(2-Quinolinylmethoxy)phenol | C16H13NO2 | 详情 | 详情 |
Extended Information