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【结 构 式】 
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【分子编号】66598 【品名】methyl 3-(4-(2-(5-ethylpyridin-2-yl)ethoxy)phenyl)propanoate 【CA登记号】 |
【 分 子 式 】C19H23NO3 【 分 子 量 】313.39656 【元素组成】C 72.82% H 7.4% N 4.47% O 15.32% |
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：(VII)
| 【1】 R4jendra GL, Pang NG, Maya JS, et al. 2004. Improved process for preparation of thiazolidinedione derivatives. W0 2004024059 |
| 【2】 Sohda T, Momose Y, Meguro K, et al. 1990. Studies on antidiabetic agents Synthesis and hypoglycemic activity of 5-[4-(pyridylaIkoxy) benzyl]-2,4-thiazolidinediones. Arzneim-Forsch, 40: 37～42 |
| 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) | 62866 | 2-(5-ethyl-2-pyridinyl)ethyl methanesulfonate | C10H15NO3S | 详情 | 详情 | |
| (II) | 11236 | 4-Nitrophenol; p-Nitrophenol | 100-02-7 | C6H5NO3 | 详情 | 详情 |
| (III) | 62867 | 5-ethyl-2-[2-(4-nitrophenoxy)ethyl]pyridine; 2-(5-ethyl-2-pyridinyl)ethyl 4-nitrophenyl ether | C15H16N2O3 | 详情 | 详情 | |
| (IV) | 62868 | 4-[2-(5-ethyl-2-pyridinyl)ethoxy]aniline; 4-[2-(5-ethyl-2-pyridinyl)ethoxy]phenylamine | C15H18N2O | 详情 | 详情 | |
| (V) | 66597 | 4-(2-(5-ethylpyridin-2-yl)ethoxy)benzenediazonium | C15H16N3O | 详情 | 详情 | |
| (VI) | 14156 | methyl acrylate | 96-33-3 | C4H6O2 | 详情 | 详情 |
| (VII) | 66598 | methyl 3-(4-(2-(5-ethylpyridin-2-yl)ethoxy)phenyl)propanoate | C19H23NO3 | 详情 | 详情 |
Extended Information