Enzalutamide Impurity D is a structurally related degradation byproduct formed via hydrolytic cleavage of the parent compound's trifluoromethyl-substituted indazole core, yielding a fluorinated aromatic ring fused to a defluorinated carboxylic acid moiety. This impurity retains a secondary amine linkage but exhibits a truncated aliphatic side chain compared to Enzalutamide. Its distinct electron-withdrawing fluorine substitution and polar carboxylic acid group confer unique chromatographic properties, enabling its use as an HPLC reference standard for quantifying synthetic process impurities in Enzalutamide formulations.
On RequestCC(C)(C(=O)O)NC1=CC(=C(C=C1)C(=O)O)F
InChI=1S/C11H12FNO4/c1-11(2,10(16)17)13-6-3-4-7(9(14)15)8(12)5-6/h3-5,13H,1-2H3,(H,14,15)(H,16,17)
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