【结 构 式】 |
【分子编号】60863 【品名】1-methyl-2-(tripropylsilyl)-1H-imidazole 【CA登记号】 |
【 分 子 式 】C13H26N2Si 【 分 子 量 】238.44842 【元素组成】C 65.48% H 10.99% N 11.75% Si 11.78% |
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:(VIII)Lithiation of 1-methylimidazole (VII), followed by quenching with triethylchlorosilane provides the 2-silyl imidazole (VIII). After metalation of (VIII) with tert-butyllithium, condensation with 4-cyanobenzaldehyde (IX) gives rise to the carbinol (X). Finally, coupling between alcohols (VI) and (X) in the presence of p-toluenesulfonic acid in refluxing toluene leads to the desired ether adduct.
【1】 Hasvold, L.A.; et al.; Design and synthesis of pyridone farnesyltransferase inhibitors. 224th ACS Natl Meet (Aug 18 2002, Boston) 2002, Abst MEDI 126. |
中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
---|---|---|---|---|---|---|
(VI) | 60862 | 5-(3-chlorophenyl)-6-(hydroxymethyl)-2-oxo-1,2-dihydro-3-pyridinecarbonitrile | C13H9ClN2O2 | 详情 | 详情 | |
(VII) | 38630 | 1-methyl-1H-imidazole | 616-47-7 | C4H6N2 | 详情 | 详情 |
(VIII) | 60863 | 1-methyl-2-(tripropylsilyl)-1H-imidazole | C13H26N2Si | 详情 | 详情 | |
(IX) | 17552 | 4-formylbenzonitrile; 4-Cyanobenzaldehyde | 105-07-7 | C8H5NO | 详情 | 详情 |
(X) | 60864 | 4-[hydroxy(1-methyl-1H-imidazol-2-yl)methyl]benzonitrile | C12H11N3O | 详情 | 详情 |
Extended Information