Total Synthesis of Chalaniline B: An Antibiotic Aminoxanthone from Vorinostat-Treated Fungus Chalara sp. 6661

Chalaniline B [1-anilino-2,8-dihydroxy-3-(hydroxymethyl)­xanthone], an antibiotic previously isolated from vorinostat-treated Chalara sp., was prepared in 7 steps from 2-hydroxyxanthone by a route incorporating regioselective oxidative transformations (bromination at C1/C3, ketone directed Pd­(II)-catalyzed hydroxylation at C8), installation of the C1-anilino moiety by a regioselective Buchwald-Hartwig amination reaction from 1,3-dibromo-2,8-dimethoxyxanthone, and late-stage hydroxymethylation at C3 using a Stille cross-coupling. Biological evaluation of deshydroxy­methyl­chalaniline B (1-anilino-2,8-dihydroxyxanthone) revealed MIC values of 8 μg mL–1 (25 μM) against both methicillin resistant S. aureus and B. subtilis.