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Synthesis of N6-alkyl-2-alkoxyadenosine compounds. In 1991, it was reported that guanosine 1 was used as a raw material and reacted with phos phorus oxy chloride to obtain 2-amino-6-chloro-9-(2', 3', 5'-tri-O-acetyl after being protected by a hydroxyl group. -β-D-ribofuranose)purine(3),3 A series of N6-alkyl-2-hydroxyadenosine compounds were synthesized through diazotization, hydrolysis and amination reactions. In 2007, it was reported that a series of 2-alkoxyadenosine compounds were synthesized by hydroxyl protection, diazotization, hydrolysis, 2-alkylation and amination reactions using 6-chloroguanosine as raw material. A2B receptor anti-inflammatory activity test research.