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【结 构 式】 
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【分子编号】66776 【品名】(7R)-6,7-dimethoxy-2,2-dimethyltetrahydro-3aH-[1,3]dioxolo[4,5-c]pyran 【CA登记号】 |
【 分 子 式 】C10H18O5 【 分 子 量 】218.24992 【元素组成】C 55.03% H 8.31% O 36.65% |
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 |
|---|---|---|---|---|---|---|
| (IX) | 37194 | (2R,3S)-5-Chloro-2-[[(4-methylbenzoyl)oxy]methyl]tetrahydro-3-furanyl 4-methylbenzoate | 4330-21-6 | C21H21ClO5 | 详情 | 详情 |
| （X） | 12204 | 5-Methyl-2,4(1H,3H)-pyrimidinedione; Thymine | 65-71-4 | C5H6N2O2 | 详情 | 详情 |
| (I) | 17520 | (3R,4S,5S)tetrahydro-2H-pyran-2,3,4,5-tetrol; L-(+)-Arabinose | 7296-56-2 | C5H10O5 | 详情 | 详情 |
| (II) | 66774 | 2-methoxytetrahydro-2H-pyran-3,4,5-triol | C6H12O5 | 详情 | 详情 | |
| (III) | 66775 | (7R)-6-methoxy-2,2-dimethyltetrahydro-3aH-[1,3]dioxolo[4,5-c]pyran-7-ol | C9H16O5 | 详情 | 详情 | |
| (IV) | 66776 | (7R)-6,7-dimethoxy-2,2-dimethyltetrahydro-3aH-[1,3]dioxolo[4,5-c]pyran | C10H18O5 | 详情 | 详情 | |
| (V) | 66777 | 6-methoxy-2,2-dimethyltetrahydro-3aH-[1,3]dioxolo[4,5-c]pyran | C9H16O4 | 详情 | 详情 | |
| (VI) | 66778 | tetrahydro-2H-pyran-2,4,5-triol | C5H10O4 | 详情 | 详情 | |
| (VII) | 12241 | (2R,3S)-2-(Hydroxymethyl)-5-methoxytetrahydro-3-furanol | C6H12O4 | 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 | |
| (XI) | 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