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【结 构 式】 
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【分子编号】66794 【品名】2-(((tert-butyldiphenylsilyl)oxy)methyl)-5-methoxytetrahydrofuran-3-ol 【CA登记号】 |
【 分 子 式 】C22H30O4Si 【 分 子 量 】386.5633 【元素组成】C 68.36% H 7.82% O 16.56% Si 7.27% |
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：(VII)
| 【1】 Storer R. Moussa A. Wang JY. et al. 2005. Synthesis of β-L-2-deoxy-nucleosides from furanoses and pyranoses via a chloro-sugar and anhydro-l-furanosyl-nucleobase intennediatcs as potential antiviral and antineoplastic agents. W0 2005003374 |
| 中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
|---|---|---|---|---|---|---|
| （X） | 12204 | 5-Methyl-2,4(1H,3H)-pyrimidinedione; Thymine | 65-71-4 | C5H6N2O2 | 详情 | 详情 |
| (I) | 17901 | Ethyl 3,3-diethoxypropanoate | 10601-80-6 | C9H18O4 | 详情 | 详情 |
| (II) | 66789 | 3,3-diethoxypropanal | C7H14O3 | 详情 | 详情 | |
| (III) | 66790 | (E)-5,5-diethoxypent-2-en-1-ol | C9H18O3 | 详情 | 详情 | |
| (IV) | 66791 | (3-(2,2-diethoxyethyl)oxiran-2-yl)methanol | C9H18O4 | 详情 | 详情 | |
| (V) | 66792 | tert-butyl((3-(2,2-diethoxyethyl)oxiran-2-yl)methoxy)diphenylsilane | C25H36O4Si | 详情 | 详情 | |
| (VI) | 66793 | 5-((tert-butyldiphenylsilyl)oxy)-3,4-dihydroxypentanal | C21H28O4Si | 详情 | 详情 | |
| (VII) | 66794 | 2-(((tert-butyldiphenylsilyl)oxy)methyl)-5-methoxytetrahydrofuran-3-ol | C22H30O4Si | 详情 | 详情 | |
| (VIII) | 62915 | {(2S,3R)-5-methoxy-3-[(4-methylbenzoyl)oxy]tetrahydro-2-furanyl}methyl 4-methylbenzoate | C22H24O6 | 详情 | 详情 | |
| (IX) | 37194 | (2R,3S)-5-Chloro-2-[[(4-methylbenzoyl)oxy]methyl]tetrahydro-3-furanyl 4-methylbenzoate | 4330-21-6 | C21H21ClO5 | 详情 | 详情 |
Extended Information