【结 构 式】 |
【分子编号】34027 【品名】(4-ethylphenyl)(2-thienyl)methanone 【CA登记号】 |
【 分 子 式 】C13H12OS 【 分 子 量 】216.30368 【元素组成】C 72.19% H 5.59% O 7.4% S 14.82% |
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:(X)The condensation of thiophene (E) and 4-ethylbenzoyl chloride (IX) by means of SnCl4 in CH2Cl2 gives (4-ethylphenyl)(2-thienyl)ketone (X), which is brominated with N-bromosuccidine and benzoyl peroxide in CCl4 to [4-(1-bromoethyl)phenyl](2-thienyl)ketone (XI); then this product is treated with NaCN in DMSO to obtain the acetonitrile (VIII), which, without purification, is hydrolyzed with H2SO4 and acetic acid.
【1】 Van Daele, P.G.H.; et al.; Synthesis of alpha-methyl-4-(2-thienylcarbonyl)benzene acetic acid, suprofen and derivatives. Arzneim-Forsch Drug Res 1975, 25, 10, 1495-1501. |
【2】 Castaner, J.; Chatterjee, S.S.; Suprofen. Drugs Fut 1976, 1, 3, 148. |
中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
---|---|---|---|---|---|---|
(E) | 13297 | Thiophene | 110-02-1 | C4H4S | 详情 | 详情 |
(VIII) | 34024 | 2-[4-(2-thienylcarbonyl)phenyl]propanenitrile | C14H11NOS | 详情 | 详情 | |
(IX) | 34026 | 4-ethylbenzoyl chloride | 16331-45-6 | C9H9ClO | 详情 | 详情 |
(X) | 34027 | (4-ethylphenyl)(2-thienyl)methanone | C13H12OS | 详情 | 详情 | |
(XI) | 34028 | [4-(1-bromoethyl)phenyl](2-thienyl)methanone | C13H11BrOS | 详情 | 详情 |
Extended Information