Methyl 2-Benzamido-2-( 1 H-benzimidazol-1-ylmethoxy ) acetate

The heterocyclic carboxylic α-aminoester methyl 2-benzamido-2-(1Hbenzimidazol-1-ylmethoxy)acetate is obtained by O-alkylation of methyl α-azido glycinate N-benzoylated with 1H-benzimidazol-1-ylmethanol.


Introduction
It is interesting to note that amino acids are components of living organisms and are precursors for protein formation.Several researchers have investigated the inhibitory potential of some amino acids and the results obtained from such studies have given some hope for the use of amino acids as green corrosion inhibitors [1][2][3][4].
Recently, benzimidazole derivatives are a key part of many drugs [5] for their potency and activation [6][7][8].Both telmisartan (TST) and candesartan (CST) are potent angiotensin II type 1 (AT1) receptor blockers (ARBs), which have been widely used in the treatment of hypertension and also found to display some other pharmacologic effects in treating diabetes [9] and heart disease [10], while DB921 with diamidine in terminal can strongly bind to the DNA groove and cause rapid destruction of the mitochondrial kinetoplast [11].
For this reason, we considered it interesting to synthesize new compounds containing 1H-benzimidazol-1-ylmethanol fused with a derivative of amino acid, in order to study their biological activities.
Following the research done on the synthesis of new α-carboxylic aminoesters [12] and in the synthesis of heterocyclic systems of benzimidazole derivatives, we reported in this paper another part
Methyl α-azido glycinate N-benzoylated 1 was obtained by the reaction [14] of sodium azide with the methyl α-bromo glycinate.The title compound is stable and can be stored for an unlimited time without any signs of decomposition.The methyl α-bromo glycinate also can be used and gives satisfactory results; the azide 1 is used especially for its stability.
As a first step and to optimize the different reaction conditions (choice of base, solvent ...), we conducted several test reactions.For all these tests, the reactions were followed by TLC and 1 H-NMR.Yields are given as pure product after column chromatography on silica gel.
After several attempts of reactions without base or in the presence of bases such as triethylamine, reaction with diisopropylethylamine (DIPEA) gave the best results.The reaction was carried out in dry acetone at room temperature for 48 h.Results are summarized in Table 1.The product 2 was obtained in 30% overall yield from 1 and was characterized by MS, 1 H-NMR and 13 C-NMR spectroscopy.

Table 1. Synthesis of
Comparing these results with the work done by our team [12,15,16], we see that we have obtained almost the same results.

Experimental
To a stirred solution of 2.86 mmol of alcohol (oxygen compound) and 3.12 mmol of diisopropylethylamine in 10 mL of dry acetone, 2.6 mmol of α-azido glycinate were added.The mixture was stirred at room temperature and the reaction was followed by TLC (Kiesegel Merck 60F254).The solvent was evaporated under reduced pressure.The residue was quenched with saturated aqueous solution of ammonium chloride (20 mL) and extracted with dichloromethane (20 mL × 3).The organic phase was dried in sodium sulfate (Na 2 SO 4 ) and the solvent was removed under reduced pressure.The product was purified by column chromatography on silica gel using ether/hexane as eluant to afford pure O-alkylated product.