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【结 构 式】

【分子编号】62711

【品名】3-[4-(3-methyl-2-thienyl)phenyl]-2-oxobutanamide

【CA登记号】

【 分 子 式 】C15H15NO2S

【 分 子 量 】273.35564

【元素组成】C 65.91% H 5.53% N 5.12% O 11.71% S 11.73%

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:(XLI)

A different strategy was based on the Knoevenagel condensation of ketone (XIV) with methyl cyanoacetate (XXXVIII) to produce the alkylidene cyanoacetate (XXXIX). Double-bond epoxidation by means of H2O2 led to (XL), which was further rearranged to keto amide (XLI). Decarboxylation of (XLI) under Hofmann rearrangement conditions furnished the arylpropionic acid (IX)

2 Arai, H.; Tanaka, K.; Watanabe, I.; Kodama, T.; Hirano, H.; Abe, N.; Nakabayashi, M. (Toyama Chemical Co., Ltd.); Novel 2-[4-(3-methyl-2-thienyl)phenyl]propionic acid and pharmaceutically acceptable salt thereof and method for treating symptoms of inflammation and pain. US 4230719 .
1 Kodama, T.; Nakabayashi, M.; Watanabe, I.; Hirano, Y.; Abe, N.; Tanaka, K.; Arai, H. (Toyama Chemical Co., Ltd.); 2-[4-(3-Methyl-2-thienyl)phenyl]propionic acid derivs. and its non-toxic salts. DE 2850485; JP 1981049376 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(IX) 62687 2-[4-(3-methyl-2-thienyl)phenyl]propanoic acid C14H14O2S 详情 详情
(XIV) 62689 1-[4-(3-methyl-2-thienyl)phenyl]-1-ethanone C13H12OS 详情 详情
(XXXVIII) 34458 Cyanoacetic acid methyl ester; methyl 2-cyanoacetate 105-34-0 C4H5NO2 详情 详情
(XXXIX) 62709 methyl (E)-2-cyano-3-[4-(3-methyl-2-thienyl)phenyl]-2-butenoate C17H15NO2S 详情 详情
(XL) 62710 methyl 2-(aminocarbonyl)-3-methyl-3-[4-(3-methyl-2-thienyl)phenyl]-2-oxiranecarboxylate C17H17NO4S 详情 详情
(XLI) 62711 3-[4-(3-methyl-2-thienyl)phenyl]-2-oxobutanamide C15H15NO2S 详情 详情
Extended Information