Novel isatin-indole derivatives as potential inhibitors of chorismate mutase (CM): their synthesis along with unexpected formation of 2-indolylmethylamino benzoate ester under Pd-Cu catalysis

• Published in: RSC advances Vol. 1; no. 1; pp. 289 - 297
• Main Authors: Reddy, Gangireddy Sujeevan, Hossain, Kazi Amirul, Kumar, Jetta Sandeep, Thirupataiah, B, Edwin, Rebecca Kristina, Giliyaru, Varadaraj Bhat, Chandrashekhar Hariharapura, Raghu, Shenoy, G. Gautham, Misra, Parimal, Pal, Manojit
• Format: Journal Article
• Language: English
• Published: England Royal Society of Chemistry 02.01.2020; The Royal Society of Chemistry
• Subjects: Alkynes; Benzoates; Catalysis; Chemistry; Coupling (molecular); Derivatives; Inhibitors; Ring opening
• ISSN: 2046-2069; 2046-2069
• DOI: 10.1039/c9ra09236f

A series of novel isatin-indole derivatives has been designed as potential inhibitors of chorismate mutase (CM) that is known to be present in bacteria, fungi and higher plants but not in human. The design was supported by in silico docking studies that predicted strong interactions of these molecules with CM. The target compounds were synthesized via the one-pot coupling/cyclization method involving the reaction of an isatin based terminal alkyne with 2-iodosulfanilides under Pd-Cu catalysis. A number of isatin-indole derivatives were prepared using this method. A side product e.g. 2-indolylmethylamino benzoate ester derivative was obtained as a result of isatin ring opening (ethanolysis) of products in certain cases. Additionally, regioselective reduction of selected compounds afforded the corresponding C-3 hydroxy derivatives. All isatin-indole derivatives showed good to high inhibition of CM in vitro among which two compounds ( 3e and 3f ) showed inhibition at nanomolar concentration. Design, synthesis and evaluation of isatin-indole derivatives were undertaken to identify potent inhibitors of chorismate mutase.