参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | 草酰氯 | HCID 65578 | — |
| 反应物 | 1,2-乙烯基二膦酸 | HCID 80247 | — |
| 反应物 | (E)-2'-DEOXY-2'-(FLUOROMETHYLENE) CYTIDINE | HCID 6435808 | — |
| 溶剂 | N,N-二甲基甲酰胺 | HCID 6228 | — |
| 产物 | HCID 86591514 | HCID 86591514 | 2.7% |
反应步骤
Ethylenediphosphonic acid (100 mg, 0.53 mmol) was treated with oxalyl chloride (2 mL, as solvent) and anhydrous DMF (0.1 mL, cat.). After heating at reflux for 10 minutes under an argon atmosphere a solution was obtained and after a further 3 h the reaction mixture was cooled to room temperature and concentrated in vacuo. The residue was coevaporated with anhydrous acetonitrile (3×10 mL). The residue was dissolved in anhydrous trimethyl phosphate (2 mL), cooled to −15° C. under an argon and (E)-2′-deoxy-2′-(fluoromethylene)cytidine (64 mg, 0.25 mmol) was added. After stirring for 2 h the reaction mixture was quenched with ice-cold TEAB solution (1.0 M, 5 mL) and stirred for 30 minutes. Purification by HPLC gave 2.9 mg of the titled compound 80.
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US07807653B2 |
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| 来源数据集 | uspto-grants-2010_10 |
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| ORD ID | ord-1d773c1d2be2451486d5fe319b1e20ef |
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| 来源说明 | uspto-grants-2010_10 |
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