Facile synthesis of N-α-boc-1,2-dialkyl-l-histidines: Utility in the synthesis of thyrotropin-releasing hormone (trh) analogs and evaluation of the cns activity

✍ Scribed by Vikramdeep Monga; Chhuttan Lal Meena; Navneet Kaur; Satyendra Kumar; Chandrashekhar Pawar; Shyam Sunder Sharma; Rahul Jain

• Publisher: Journal of Heterocyclic Chemistry
• Year: 2008
• Tongue: English
• Weight: 271 KB
• Volume: 45
• Category: Article
• ISSN: 0022-152X
• DOI: 10.1002/jhet.5570450608

✦ Synopsis

Abstract

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A facile synthesis of N‐α‐Boc‐1,2‐dialkyl‐L‐histidines starting from N‐α‐trifluoroacetyl‐L‐histidine methyl ester is reported. The key steps involve direct and regiospecific N‐1(τ) ring‐alkylation of the N‐α‐trifluoroacetyl‐L‐histidine‐methyl ester by suitable alkyl iodide in the presence of NaH in DMF at −15 °C followed by homolytic free radical C‐2 alkylation via a silver catalyzed oxidative decarboxylation of alkylcarboxylic acid in the presence of ammonium persulfate under acidic conditions. The application of newly synthesized bioimidazoles was illustrated by their incorporation into thyrotropin‐releasing hormone (TRH). The synthesized TRH analogs were evaluated in vivo for analeptic activity. We report discovery of a TRH analog, which was found to potentiate the pentobarbital‐induced sleep in vivo.