Facile synthesis of 9-(N-amino-4-fluoromethyl-3-pyrrolidinyl)-2-fluoro-6-aminopurine from trans-4-hydroxy-L-proline

Ye Qing Li Ming Lu Chun Xu Lu Sai Jian Zhu Qi Fa Liu

引用本文: Ye Qing Li,  Ming Lu,  Chun Xu Lu,  Sai Jian Zhu,  Qi Fa Liu. Facile synthesis of 9-(N-amino-4-fluoromethyl-3-pyrrolidinyl)-2-fluoro-6-aminopurine from trans-4-hydroxy-L-proline[J]. Chinese Chemical Letters, 2007, 18(11): 1313-1315. doi: 10.1016/j.cclet.2007.09.020 shu
Citation:  Ye Qing Li,  Ming Lu,  Chun Xu Lu,  Sai Jian Zhu,  Qi Fa Liu. Facile synthesis of 9-(N-amino-4-fluoromethyl-3-pyrrolidinyl)-2-fluoro-6-aminopurine from trans-4-hydroxy-L-proline[J]. Chinese Chemical Letters, 2007, 18(11): 1313-1315. doi: 10.1016/j.cclet.2007.09.020 shu

Facile synthesis of 9-(N-amino-4-fluoromethyl-3-pyrrolidinyl)-2-fluoro-6-aminopurine from trans-4-hydroxy-L-proline

摘要: A novel and simple procedure for synthesis of azanucleoside by Mitsunobu reaction between N-(p-nitrobenzyloxycarbonyl)-trans-4-hydroxy-D-proline methyl ester obtained from trans-4-hydroxy-L-proline after six-step reaction and 2-fluoro-6-azidopurine is described, and azanucleoside is fluorinated by new fluridizer 2, 2-difluoro-1, 3-dimethylimidazolidine (DFI). All reactions could be carried out under mild condition.

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  • 收稿日期:  2007-04-29
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    沈阳化工大学材料科学与工程学院 沈阳 110142

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