Synthesis and antimicrobial evaluation of some new oxadiazoles derived from phenylpropionohydrazides.

In this study a series ofnew1-(2-aryl-5-phenethyl-1,3,4-oxadiazol-3(2H)-yl)ethanones 2a-e was synthesized by the cyclization of imines 1a-e using acetic anhydride. The products were evaluated for anti-bacterial and anti-fungal activity. Among the newly synthesized compounds, 1-(2-(4-(dimethylamino)phenyl)-5-phenethyl-1,3,4-oxadiazol-3(2H)-yl)ethanone (2a)and1-(2-(4-chlorophenyl)-5-phenethyl-1,3,4-oxadiazol-3(2H)-yl)ethanone (2b)were found to possess maximum activity against the tested strains of S. aureus and P. aeruginosa. It was concluded that para-substitution enhances the activity of synthesized oxadiazoles.

1. Introduction

It is an established fact that oxadiazoles, pan class="Chemical">imines and propanoates exhibits antimitotic [1], antikinetoplastid [2], antitussive [3], hybrid COX-2 inhibitor/nitric oxide donor [4], antimycotic [5], anti-inflammatory [6], analgesic [7], antimicrobial and anticonvulsant [8,9,10,11,12] activities. Moreover esters and hydrazides can be converted into imines, which are precursor for oxadiazoles [8,9,10,11,12]. The literature has reported different biological activities and method of synthesis for oxadiazoles [1,2,3,4,5,6,7,8,9,10,11,12]. Hence an attempt was made to convert some N-(substituted benzylidene)-3-phenylpropionohydrazides into novel 1-(2-aryl-5-phenethyl-1,3,4-oxadiazol-3(2H)-yl)ethanones. The novel compounds were characterized and further investigated for anti-bacterial and anti-fungal activities.

2. Results and Discussion

2.1. Chemistry

The treatment of N-(substituted benzylidene)-3-phenylpropionohydrazides 1a-e, with pan class="Chemical">acetic anhydride yielded 1-(2-aryl-5-phenethyl-1,3,4-oxadiazol-3(2H)-yl)ethanones 2a-e (Scheme 1).

Scheme 1

Synthesis of Oxadiazoles 2a-e.

The carbonylamino and imino groups in compounds 1a-e, were found to cyclize to form pan class="Chemical">oxadiazole rings when reacted with acetic anhydride. The assigned structures, molecular formulae and the anomeric configuration of the newly synthesized oxadiazoles 2a-e were further confirmed and supported by mass, 1H-NMR and IR spectrometry. The fragmentation pattern of compound 2a due to absence of C8H9, C12H13N2O2, C16H19N, C12H14N3O2, C13H16N3O2, C15H18N3O2 groups given in Figure 1, as an example further supported in identification of molecular structures of compounds 2a-e.

Figure 1

fragmentation pattern of oxadiazole 2a.

The absence of specific group fragments in the mass spectra of compounds 2b-e (C8H9, C12pan class="Species">H13N2O2, C14H13Cl, C10H8ClN2O2, C11H10ClN2O2, C13H12ClN2O2 in the case of 2b; C8H9, C12H13N2O2, -C14H14O2, C10H9N2O4, C11H11N2O4, C13H13N2O4 in 2c; C8H9, C12H13N2O2, C14H14, C10H9N2O2, C11H11N2O2, C13H13N2O2 2d; and C8H9, C12H13N2O2, C14H14O, C10H9N2O3, C11H11N2O3, C13H13N2O3 in 2e) was a key to establish their molecular structures. The purity of the compounds was checked by melting point, TLC and elemental analysis results, which were within ± 0.4% of the theoretical values.

2.2. Biological activity

The newly synthesized compounds 2a-e were screened for antibacterial activity against freshly cultured strains of S. aureus (SA) and pan class="Species">P. aeruginosa (PA) using sterile nutrient agar media and for antifungal activity against freshly cultured strains of C. albicans (CA) and A. flavus (AF) using sterile sabouraud’s agar medium by the disk diffusion method at a concentration of 2 mg per mL. using DMF as solvent. The results were recorded in duplicate using ampicillin and fluconazole at a concentration of 1 mg per mL as standards.

Among newly synthesized derivatives, compounds 2a and 2b were found to be equipotent to ampicillin when tested against the strains of pan class="Species">S. aureus, and P. aeruginosa, whereas some of the newly synthesized compounds like 2a, 2d and 2e were found to possess good antibacterial and antifungal activity when tested against S. aureus, P. aeruginosa, C. albicans and A. flavus (Table 1).

Table 1

Antimicrobial activity-sensitivity testing of 2a-e.

CompoundNo.	Zone of inhibition in mm
	Antibacterial Activity		Antifungal Activity
	SA	PA	CA	AF
2a	24	24	16	15
2b	25	24	15	13
2c	23	20	13	12
2d	22	23	16	13
2e	19	20	16	15
Ampicillin	25	24	-	-
Fluconazole	-	-	17	16

3. Experimental Section

3.1. General

Melting points of newly synthesized compounds were determined using Thomas Hoover apparatus. IR spectra were recorded (in KBr) on a Bruker PCIR, 1H-NMR on Bruker, DPX 300 and mass spectra on MASPEC (MSW/9629). Purity of synthesized compounds was checked by TLC pan class="Chemical">aluminium sheets – silica gel 60 F254 (0.2 mm).

3.2. General procedure for the synthesis of 1-(2-aryl-5-phenethyl-1,3,4-oxadiazol-3(2H)-yl)ethanones (

A mixture of compound 1a-e (0.01 mol) derived from 3-phenyl propane hydrazide was refluxed with pan class="Chemical">acetic anhydride (0.01 mol) for 12 hours in the presence of zinc chloride. The product formed was isolated by filtration and recrystallized from methanol to yield compounds 2a-e.

1-(2-(4-(Dimethylamino)phenyl)-5-phenethyl-1,3,4-oxadiazol-3(2H)-yl)ethanone (2a): pan class="Species">Pale yellow crystals; Yield 65.8%; mp 225-226ºC; 1H-NMR δ (ppm): 2.04 (3H, s, -CO-CH3), 2.32 (2H, t, 6.9Hz, -CH2-C-O-), 2.65 (2H, t, 6.9Hz, Ar-CH2), 2.89 (6H, s, -N(CH3)2), 6.52 (2H, d, 8.1Hz, Ar-H3′ & 5′), 6.65 (1H, s, -N-CH-Ar′), 7.01 (2H, d, 8.2Hz, Ar′-H2′ & 6′), 7.18-7.31 (5H, m, Ar-H2, 3, 4, 5 & 6); FT-IR: 2924 (C-H of CH2), 1688 (C=O), 1611 (C=N), 1259 (C-O-C) cm-1; Anal. Calcd. for C20H23N3O2 (337.42): C: 71.19, H: 6.87, N: 12.45. found: C: 71.16, H: 6.85, N: 12.43; MS: m/z: 337 (M+), 232 (base peak), 120, 112, 105, 91, 65.

1-(2-(4-Chlorophenyl)-5-phenethyl-1,3,4-oxadiazol-3(2H)-yl)ethanone (2b): White crystals; Yield 64.9%; mp 212-213 °C; pan class="Chemical">1H-NMR δ (ppm): 2.11 (3H, s, -CO-CH3), 2.38 (2H, t, 6.5Hz, -CH2-C-O-), 2.72 (2H, t, 6.6Hz, Ar-CH2), 6.64 (1H, s, -N-CH-Ar′), 7.14 (2H, d, 8.3Hz, Ar′-H2′ & 6′), 7.20 (2H, d, 8.1Hz, Ar′-H3′ & 5′), 7.24-7.37 (5H, m, Ar-H2, 3, 4, 5 & 6); FT-IR: 1608 (C=N), 2928 (C-H of CH2), 1681 (C=O), 1256 (C-O-C) cm-1; Anal. Calcd. for C18H17N2O2Cl (328.79): C: 65.75, H: 5.21, N: 8.52. Found: C: 65.72, H: 5.20, N: 8.50; MS: m/z 328 (M+), 223 (base peak), 112, 111, 105, 91, 65.

1-(2-(2,4-Dihydroxyphenyl)-5-phenethyl-1,3,4-oxadiazol-3(2H)-yl) ethanone (2c): Yellow brown crystals; Yield 59.2%; mp 219-220 °C; 1H-NMR δ (ppm): 2.07 (3H, s, -CO-CH3), 2.32 (2H, t, 6.8Hz, -CH2-C-O-), 2.62 (2H, t, 6.8Hz, Ar-CH2), 5.22 (pan class="Chemical">1H, s, 4-OH), 5.28 (1H, s, 2-OH), 6.14 (1H, d, 2.6 Hz, Ar′-H3′), 6.28 (1H, dd, 2.8, 7.6Hz, Ar′-H5′), 6.60 (1H, s, -N-CH-Ar′), 6.88 (1H, d, 7.9 Hz, Ar′-H6′), 7.19-7.32 (5H, m, Ar-H2, 3, 4, 5 & 6 ); FT-IR: 3516 (OH), 2926 (C-H of CH2), 1683 (C=O), 1617 (C=N), 1253 (C-O-C) cm-1; Anal. Calcd. for C18H18N2O4 (326.34): C: 66.25, H: 5.56, N: 8.58. Found: C : 66.22, H : 5.52, N : 5.54; MS: m/z 326 (M+), 221 (base peak), 112, 109, 105, 91, 65.

1-(5-Phenethyl-2-phenyl-1,3,4-oxadiazol-3(2H)-yl)ethanone (2d): White crystals; Yield 60.3%; mp 203-204 °C; 1H-NMR δ (ppm): 2.02 (3H, s, -CO-CH3), 2.30 (2H, t, 6.4Hz, -CH2-C-O-), 2.61 (2H, t, 6.5Hz, Ar-CH2), 6.61 (pan class="Chemical">1H, s, -N-CH-Ar′), 7.15-7.29 (10H, m, Ar′ -H2′, 3′, 4′, 5′ & 6′ & Ar -H2, 3, 4, 5 & 6); FT-IR: 1610 (C=N), 2925 (C-H of CH2), 1686 (C=O), 1249 (C-O-C) cm-1; Anal. Calcd. for C18H18N2O2 (294.35): C: 73.45, H: 6.16, N: 9.52. Found: C: 73.42, H: 6.14, N: 9.50; MS: m/z 294 (M+), 189 (base peak), 105, 91, 77, 65.

1-(2-(4-Hydroxyphenyl)-5-phenethyl-1,3,4-oxadiazol-3(2H)-yl)ethanone (2e): Orange crystals; Yield 62.4%; mp 213-214 °C; 1H-NMR δ (ppm): 2.05 (3H, s, -CO-CH3), 2.35 (2H, t, 6.6Hz, -CH2-C-O-), 2.67 (2H, t, 6.5Hz, Ar-CH2), 5.26 (pan class="Chemical">1H, s, 4-OH), 6.61 (1H, s, -N-CH-Ar′), 6.68 (2H, d, 7.8Hz, Ar′-H3′ & 5′), 7.03 (2H, d, 7.5Hz, Ar′-H2′ & 6′), 7.16-7.29 (5H, m, Ar-H2, 3, 4, 5 & 6); FT-IR: 3512 (OH), 2920 (C-H of CH2), 1680 (C=O), 1613 (C=N), 1249 (C-O-C) cm-1; Anal. Calcd. for C18H18N2O3 (310.34): C: 69.66, H: 5.85, N: 9.03. Found: C: 69.64, H: 5.82, N: 9.01; MS: m/z 310 (M+), 205 (base peak), 112, 105, 93, 91, 65.

4. Conclusions

Both analytical and spectral data (IR, pan class="Chemical">1H-NMR, MS) of all the synthesized compounds were in full agreement with the proposed structure. After comparing the antimicrobial results of compounds 2a-e, it was concluded that the incorporation of an oxadiazole moiety in phenylpropionyl derivatives enhances their antimicrobial activity and also para-substitution in the Ar′ group of the oxadiazoles was found to enhance their potency, especially in compound 2a and 2b. Further studies to acquire more information about structure activity relationship are in progress in our laboratory.