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【结 构 式】 
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【分子编号】66788 【品名】3,5-bis(benzyloxy)-2-((benzyloxy)methyl)tetrahydrofuran 【CA登记号】 |
【 分 子 式 】C26H28O4 【 分 子 量 】404.506 【元素组成】C 77.20% H 6.98% O 15.82% |
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：(XI)
| 【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） | 62916 | {(2S,3R)-5-hydroxy-3-[(4-methylbenzoyl)oxy]tetrahydro-2-furanyl}methyl 4-methylbenzoate | C21H22O6 | 详情 | 详情 | |
| (I) | 66781 | 5-(1,2-dihydroxyethyl)-3,4-dihydroxydihydrofuran-2(3H)-one | C6H10O6 | 详情 | 详情 | |
| (II) | 66782 | 3-bromo-5-(2-bromo-1-hydroxyethyl)-4-hydroxydihydrofuran-2(3H)-one | C6H8Br2O4 | 详情 | 详情 | |
| (III) | 66783 | 2,6-dibromo-3,4,5-trihydroxyhexanehydrazide | C6H12Br2N2O4 | 详情 | 详情 | |
| (IV) | 66784 | 5-(2-bromo-1-hydroxyethyl)-4-hydroxydihydrofuran-2(3H)-one | C6H9BrO4 | 详情 | 详情 | |
| (V) | 66785 | potassium 3,4-dihydroxy-4-(oxiran-2-yl)butanoate | C6H9KO5 | 详情 | 详情 | |
| (VI) | 66786 | potassium 3-hydroxy-3-(3-(hydroxymethyl)oxiran-2-yl)propanoate | C6H9KO5 | 详情 | 详情 | |
| (VII) | 66787 | 5-(1,2-dihydroxyethyl)-4-hydroxydihydrofuran-2(3H)-one | C6H10O5 | 详情 | 详情 | |
| (VIII) | 66772 | 4-hydroxy-5-(hydroxymethyl)dihydrofuran-2(3H)-one | C5H8O4 | 详情 | 详情 | |
| (IX) | 66773 | C21H21O6 | 详情 | 详情 | ||
| (XI) | 66788 | 3,5-bis(benzyloxy)-2-((benzyloxy)methyl)tetrahydrofuran | C26H28O4 | 详情 | 详情 |
Extended Information