首页> 外国专利> METHOD FOR SYNTHESIZING 2-CHLORO-9-(2-DEOXY-2-FLUORO-beta-D-ARABINOFURANOSYL)-9H-PURINE-6-AMINE

METHOD FOR SYNTHESIZING 2-CHLORO-9-(2-DEOXY-2-FLUORO-beta-D-ARABINOFURANOSYL)-9H-PURINE-6-AMINE

机译:合成2-氯-9-(2-脱氧-2-氟-β-D-阿拉伯呋喃糖基)-9H-嘌呤-6-胺的方法

摘要

PPROBLEM TO BE SOLVED: To provide a method for synthesizing a 2-chloro-9-(2-deoxy-2-fluoro--D-arabinofuranosyl)-9H-purine-6-amine in a comparatively high yield. PSOLUTION: In the method for synthesizing a 2-chloro-9-(2-deoxy-2-fluoro--D-arabinofuranosyl)-9H-purine-6-amine, (a) an anion of 2-chloro-6-substituted purine (here, the substituent of the 6-position of the 2-chloro-6-substituted purine is selected from the group consisting of an amino group and a protected amino group) is reacted with protected and activated 2-deoxy-2-fluoro-D-arabinofuranose and then with (b) ammonia to obtain 2-chloro-9-(2-deoxy-2-fluoro--D-arabinofuranosyl)-9H-purine-6-amine. PCOPYRIGHT: (C)2010,JPO&INPIT
机译:

要解决的问题:提供一种以相对较高的产率合成2-氯-9-(2-脱氧-2-氟-D-阿拉伯呋喃糖基)-9H-嘌呤-6-胺的方法。

解决方案:在合成2-氯-9-(2-脱氧-2-氟-D-阿拉伯呋喃糖基)-9H-嘌呤-6-胺的方法中,(a)2-氯-阴离子使6-取代的嘌呤(此处,2-氯-6-取代的嘌呤的6-位的取代基选自氨基和受保护的氨基)与受保护和活化的2-脱氧- 2-氟-D-阿拉伯呋喃糖,然后与(b)氨水制得2-氯-9-(2-脱氧-2-氟-D-阿拉伯呋喃糖基)-9H-嘌呤-6-胺。

版权:(C)2010,日本特许厅&INPIT

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