Synthesis of Pyrrolopyrimidine Derivatives
Structure-based design of novel Chk1 inhibitors Insights into hydrogen bonding and protein-ligand affinity
Scheme 2
The pyrrolopyrimidines were prepared from the commercially available analogue 21 (Scheme 2). This was debenzylated with aluminum chloride in refluxing toluene to give the derivative 22 in 54% yield, based on the recovered starting material. The anilino derivatives were prepared by microwave irradiation of precursor 22 with 6 equiv of the corresponding amine in ethanol at 100 °C. Purification of the crude material using column chromatography gave the pure pyrrolopyrimidines in 10-20% yield.
Copyright © 2008-2026 LookChem.com All rights reserved.