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【结 构 式】 
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【分子编号】49905 【品名】[4-methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methanol 【CA登记号】 |
【 分 子 式 】C12H10F3NOS 【 分 子 量 】273.2787496 【元素组成】C 52.74% H 3.69% F 20.86% N 5.13% O 5.85% S 11.73% |
合成路线1
该中间体在本合成路线中的序号：(XIV)4-Trifluoromethylbenzamide (X) was converted to the corresponding thioamide (XI) by treatment with P4S10. Condensation of (XI) with ethyl 2-chloroacetoacetate (XII) provided thiazole (XIII). Subsequent reduction of the ester group of (XIII) with LiAlH4 gave alcohol (XIV). Conversion of (XIV) to the corresponding chloride (XV) was carried out by reaction with methanesulfonyl chloride and triethylamine. Chloride (XV) was then condensed with thiophenol (VII) in the presence of Cs2CO3 to yield thioether (XVI). The methyl ester group was finally hydrolyzed to the title acid employing LiOH.
| 【1】 Maloney, P.R.; Gellibert, F.J.; Sierra, M.L.; Chao, E.Y.-H.; Haffner, C.D.; Willson, T.M.; Sznaidman, M.L.; Xu H.E.; Lambert, M.H. III; Sternbach, D.D. (Glaxo Group Ltd.); Thiazole and oxazole derivs. and their pharmaceutical use. WO 0100603 . |
| 中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
|---|---|---|---|---|---|---|
| (VII) | 49899 | methyl 2-(2-methyl-4-sulfanylphenoxy)acetate | C10H12O3S | 详情 | 详情 | |
| (X) | 49902 | alpha,alpha,alpha-Trifluoro-p-toluamide; 4-Trifluoromethylbenzamide | 1891-90-3 | C8H6F3NO | 详情 | 详情 |
| (XI) | 49903 | 4-(Trifluoromethyl)thiobenzamide | 72505-21-6 | C8H6F3NS | 详情 | 详情 |
| (XII) | 21337 | ethyl 2-chloro-3-oxobutanoate | 609-15-4 | C6H9ClO3 | 详情 | 详情 |
| (XIII) | 49904 | Ethyl 4-methyl-2-[4-(trifluoromethyl)phenyl]-thiazole-5-carboxylate | 175277-03-9 | C14H12F3NO2S | 详情 | 详情 |
| (XIV) | 49905 | [4-methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methanol | C12H10F3NOS | 详情 | 详情 | |
| (XV) | 49906 | 5-(chloromethyl)-4-methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazole | C12H9ClF3NS | 详情 | 详情 | |
| (XVI) | 49907 | methyl 2-[2-methyl-4-[([4-methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methyl)sulfanyl]phenoxy]acetate | C22H20F3NO3S2 | 详情 | 详情 |