【结 构 式】 |
【分子编号】36178 【品名】ethyl (2R,4R)-5-chloro-2,4-dimethyl-5-oxopentanoate 【CA登记号】 |
【 分 子 式 】C9H15ClO3 【 分 子 量 】206.669 【元素组成】C 52.31% H 7.32% Cl 17.15% O 23.22% |
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)The ethanolysis of 2,4-dimethylglutaric anhydride (I) gives the monoethyl ester of 2,4-dimethylglutaric acid (II), which by reaction with oxalyl chloride is converted into the monoacyl chloride (III). Finally, this compound is condensed with indoline-2-carboxylic acid (IV) hy means of K2CO3 in pyridine.
【1】 Gruenfeld, N (Novartis AG); 1-Carboxyalkanoylindolin-2-carboxylic acids and derivs. thereof, processes for their preparation, and pharmaceutical compsns. containing these cpds. as well as their use. EP 0050850 . |
【2】 Serradell, M.N.; Castaner, J.; Blancafort, P.; CGS-13945. Drugs Fut 1983, 8, 12, 1010. |
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) | 36176 | 3,5-dimethyldihydro-2H-pyran-2,6(3H)-dione | C7H10O3 | 详情 | 详情 | |
(II) | 36177 | (2R,4R)-5-ethoxy-2,4-dimethyl-5-oxopentanoic acid | C9H16O4 | 详情 | 详情 | |
(III) | 36178 | ethyl (2R,4R)-5-chloro-2,4-dimethyl-5-oxopentanoate | C9H15ClO3 | 详情 | 详情 | |
(IV) | 34307 | (2S)-2,3-dihydro-1H-indole-2-carboxylic acid | C9H9NO2 | 详情 | 详情 |
Extended Information