Method for synthesizing 2/6-iodo-purine derivative through visible light induced hydrazine removal-iodination reaction
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- XINXIANG UNIV
- Publication Date
- 2022-07-22
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Abstract
Description
technical field
[0001] The invention belongs to the technical field of drug synthesis, in particular to a method for synthesizing 2 / 6-iodopurine derivatives by visible light-induced dehydration-iodination reaction. Background technique
[0002] Iodopurine is an important intermediate in the synthesis of nucleoside drugs, which is divided into 6-iodo, 8-iodo and 2-iodopurine and purine nucleosides. Through metal coupling reactions such as Suzuki and Sonogashira, alkenyl Hydrophobic groups such as alkynyl groups, alkynyl groups, and fused-ring aryl groups are easily connected to purines to obtain drugs with higher physiological activity and better curative effect, or further convert them into fluorescent molecules that can be used as DNA probes. It has a wide range of applications in therapy, biochemistry and chemical synthesis. At present, the synthesis of iodopurine derivatives is usually divided into four types of reaction systems:
[0003] 1. Utilize amino group to repla...