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【结 构 式】 
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【分子编号】30241 【品名】3-[[1-(2-methylphenyl)-1H-imidazol-2-yl]sulfinyl]propyl methanesulfonate 【CA登记号】 |
【 分 子 式 】C14H18N2O4S2 【 分 子 量 】342.44 【元素组成】C 49.1% H 5.3% N 8.18% O 18.69% S 18.73% |
合成路线1
该中间体在本合成路线中的序号：(XX)Alternatively, the intermediate chiral hydroxy sulfoxide (XIX) was prepared by the following procedures. Alkylation of mercaptoimidazole (I) with 3-chloropropanol (XVII) gave thioether (XVIII). This was oxidized with cumene hydroperoxide and titanium tetraisopropoxide in the presence of either D-diethyl tartrate or (R)-mandelic acid as the chiral auxiliaries to provide, after recrystallization from methyl ethyl ketone, the optically pure sulfoxide (XIX). Subsequent treatment with methanesulfonyl chloride and triethylamine gave mesylate (XX), which was finally condensed with the sodium salt of 6-hydroxytetrahydroquinolinone (XXI) in DMSO at 60 C.
| 【1】 Matsugi, M.; et al.; Practical asymmetric oxidation of 3-[1-(2-methylphenyl)imidazol-2-ylthio]propan-1-ol based on a titanium-mandelic acid complex. Tetrahedron Lett 1998, 39, 31, 5591. |
| 【2】 Nishi, T.; Uno, T.; Shu, Y.; Tamura, K.; Okada, M. (Otsuka Pharmaceutical Co., Ltd.); Carbostyril derivs.. EP 0651747; JP 1995033765; US 5541198; WO 9426732 . |
| 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) | 30223 | 1-(2-methylphenyl)-1H-imidazol-2-ylhydrosulfide; 1-(2-methylphenyl)-1H-imidazole-2-thiol | C10H10N2S | 详情 | 详情 | |
| (XVII) | 19490 | 3-chloro-1-propanol | 627-30-5 | C3H7ClO | 详情 | 详情 |
| (XVIII) | 30239 | 3-[[1-(2-methylphenyl)-1H-imidazol-2-yl]sulfanyl]-1-propanol | C13H16N2OS | 详情 | 详情 | |
| (XIX) | 30240 | 3-[[1-(2-methylphenyl)-1H-imidazol-2-yl]sulfinyl]-1-propanol | C13H16N2O2S | 详情 | 详情 | |
| (XX) | 30241 | 3-[[1-(2-methylphenyl)-1H-imidazol-2-yl]sulfinyl]propyl methanesulfonate | C14H18N2O4S2 | 详情 | 详情 | |
| (XXI) | 30242 | sodium 2-oxo-1,2,3,4-tetrahydro-6-quinolinolate | C9H8NNaO2 | 详情 | 详情 |