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【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