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【结 构 式】 
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【分子编号】66797 【品名】 【CA登记号】 |
【 分 子 式 】C15H20O3 【 分 子 量 】248.322 【元素组成】C 72.55% H 8.12% O 19.33% |
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：(IV)
| 【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) | 11471 | 1,4-Pentadien-3-ol | 922-65-6 | C5H8O | 详情 | 详情 |
| (II) | 66795 | (S)-1-((S)-oxiran-2-yl)prop-2-en-1-ol | C5H8O2 | 详情 | 详情 | |
| (III) | 66796 | (2R,3S)-1-(benzyloxy)pent-4-ene-2,3-diol | C12H16O3 | 详情 | 详情 | |
| (IV) | 66797 | C15H20O3 | 详情 | 详情 | ||
| (V) | 66798 | 2-((4R,5R)-5-((benzyloxy)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)acetaldehyde | C15H20O4 | 详情 | 详情 | |
| (VI) | 66799 | (5R)-5-((benzyloxy)methyl)tetrahydrofuran-2,4-diol | C12H16O4 | 详情 | 详情 | |
| (VII) | 66800 | (2R)-2-((benzyloxy)methyl)-5-methoxytetrahydrofuran-3-ol | C13H18O4 | 详情 | 详情 | |
| (VIII) | 12241 | (2R,3S)-2-(Hydroxymethyl)-5-methoxytetrahydro-3-furanol | C6H12O4 | 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 |
| (XIV) | 62918 | {(2S,3R,5S)-3-[(4-methylbenzoyl)oxy]-5-[5-methyl-2,4-dioxo-3,4-dihydro-1(2H)-pyrimidinyl]tetrahydro-2-furanyl}methyl 4-methylbenzoate | C26H26N2O7 | 详情 | 详情 |
Extended Information