90213-69-7

Upstream product

• 70613-79-5 2,3,5-tri-O-benzyl-D-arabinofuranosyl bromide 
• 90213-66-4 2,4-dichloro-7H-pyrrolo[2,3-d]pyrimidine 
• 84955-31-7 4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-amine 
• 52522-49-3 2,3,5-tri-O-benzyl-1-(4-nitrobenzoyloxy)-D-arabinofuranose 

Downstream Products

• 90213-71-1 2-Chlor-4-amino-7-(2,3,5-tri-O-benzyl-β-D-arabinofuranosyl)-7H-pyrrolo<2,3-d>pyrimidin 
• 90213-72-2 2,4-Diamino-7-(2,3,5-tri-O-benzyl-β-D-arabinofuranosyl)-7H-pyrrolo<2,3-d>pyrimidin 

Relevant academic research and scientific papers

7-(β-D-Arabinofuranosyl)-2,4-dichloro-7H-pyrrolopyrimidine - Synthesis, Selective Displacement of Halogen, and Influence of Glyconic Protecting Groups on the Reactivity of the Aglycone

Selective N-7 glycosylation of 2,4-dichloro-7H-pyrrolopyrimidine (1a) with the arabinohalogenose 5 has been achieved yielding the β-anomer 7a in 67percent yield.Debenzylation with boron trichloride results in the formation of the 2,4-dichloronucleo