Heteroatom Chemistry

Heteroatom Chemistry / 2019 / Article

Research Article | Open Access

Volume 2019 |Article ID 2326514 | https://doi.org/10.1155/2019/2326514

Heba E. Hashem, Ahmed M. Abo-Bakr, "Synthesis of Some New 1,2,4-Triazine and 1,2,5-Oxadiazine Derivatives with Antimicrobial Activity", Heteroatom Chemistry, vol. 2019, Article ID 2326514, 7 pages, 2019. https://doi.org/10.1155/2019/2326514

Synthesis of Some New 1,2,4-Triazine and 1,2,5-Oxadiazine Derivatives with Antimicrobial Activity

Academic Editor: Xing-Hai Liu
Received19 Jun 2019
Accepted21 Aug 2019
Published25 Sep 2019


1,2,4-Triazine and 1,2,5-oxadiazine derivatives 2–12 were obtained from treated 1,3-oxazolone (1) with phenyl hydrazine or hydroxylamine hydrochloride. Chlorotriazine derivative 3 undergoing condensation reactions with different reagents produced new fused tetrazolo-triazine and triazino-quinazolinone derivatives. 1,2,5-Oxadiazine has been used as a synthon for the fused pyrazolo-oxadiazine derivative. The constitution of the prepared compounds was built up based on microanalytical and spectral data. Some of the new compounds were assessed for their antimicrobial activity.

1. Introduction

The importance of studying the azlactones’ chemistry remains unabated because of their uses as intermediates for synthesis of new heterocyclic and fused heterocyclic compounds. 1,2,4-Triazine derivatives exhibit antifungal [1, 2], anti-HIV [3], anticancer [4], anti-inflammatory [5], analgesic [6], and antihypertensive [7] activities, besides their uses as herbicides, pesticides, and dyes [8, 9]. The pharmacological efficacy of oxadiazine is also known; derivatives of 1,3,4-oxadiazine exhibit antibacterial, cardiovascular plant growth-regulating, miticidal, nematocidal, insecticidal, and anticonvulsive activities [10, 11]. In addition, oxadiazines are valuable intermediates in the synthesis of tenidap prodrugs or lactam anti-infection agents, specifically in the synthesis of carbapenems and penems [1214]. On the contrary, 1,2,5-oxadiazines are not very common heterocyclic systems.

A comprehensive review of the synthesis and reactivity of these systems has been reported by Smalley [15]. In view of these observations, the present work tends to utilize “(Z)-4-(4-methoxybenzylidene)-2-phenyloxazol-5(4H)-one” [16] for the synthesis of new 1,2,5-oxadiazine and 1,2,4-triazine derivatives.

2. Results and Discussion

“(Z)-4-(4-Methoxybenzylidene)-2-phenyloxazol-5(4H)-one” (1) is synthesized via reaction of hippuric acid with p-anisaldehyde under Perkin–Erlenmeyer reaction conditions as reported in the literature [16].

Reaction of oxazolone 1 with phenyl hydrazine in acetic acid (glacial) and fused sodium acetate afforded the 1,2,4-triazine-6(5H)-one derivative (2). Compound 2 could be present in lactam-lactim tautomers (2A and 2B), but the lactam form is thermodynamically more stable because the oxo form is more stabilized by 54.4 kJ mol−1 than the enol form [17]. The structure of 2 can be deduced from its spectroscopic properties. The IR spectrum showed a band correlated with C=O lactam at 1690 cm−1. Furthermore, 1HNMR spectrum showed one broad singlet signal in the downfield region correlated with the NH proton.

Refluxing of compound 2 with phosphorus oxychloride and phosphorus pentachloride produces the chlorotriazine derivative 3 which is used as a synthon for new triazine derivatives (Scheme 1). Reaction of chlorotriazine 3 with hydrazine hydrate gave the hydrazine derivative 4. Spectral data of compound 4 established its suggested structure. Its IR spectrum exhibited absorption bands belonging to NH, NH2, and C=N groups. The 1HNMR spectrum exhibited exchangeable broad singlet signals corresponding to the two protons of NH2 and other in the downfield region for the NH proton.

The structure of compound 4 established chemically by refluxing in acetic anhydride yielded the N,N′-diacetyl derivative 5 (Scheme 2). The structure of compound 5, also deduced from the IR spectrum, showed two strong absorption bands at 1726, 1701 cm−1 for the C=O group (due to symmetric and antisymmetric stretching of the N-diacetyl group).

1HNMR spectra exhibited a strong singlet signal (δ 2.28 ppm) for the two magnetically equivalent CH3 protons, besides one broad singlet signal for the NH proton. The mass spectrum confirmed the assigned structure of 5 (shown in Experimental).

Also, treatment of chlorotriazine 3 with sodium azide in acetic acid gave 8-(4-methoxybenzylidene)-5,8-dihydro-5,6-diphenyltetrazolo[1,5-f][1,2,4]triazine (6) (Scheme 3).

It is interesting to note that refluxing chlorotriazine (3) with anthranilic acid in “acetic acid” gave the triazino-quinazolinone derivative 7. The structure of compound 7 is elucidated from the spectral data. Infrared spectrum showed absorption bands characteristic of υ C=O at 1678 cm−1.

In addition, the 1HNMR spectrum of compound 7 showed the different protons from low- to high-field signals for aromatic and aliphatic protons in harmony with the proposed structure. The mass spectrum of compound 7 gave us a good indication about stability of that structure, where the molecular ion peak together with some important peaks was displayed (base peak).

Treatment of oxazolone 1 with NH2OH·HCl in pyridine afforded the Z-configurated isomer adduct which could have one of the two possible structures, oxadiazone Z-8 or imidazolone Z-9 (Scheme 4). The infrared spectrum exhibited two bands at 3240 cm−1 for NH and 1700 cm−1 for the CO group. The lower frequency of the carbonyl group supported the six-membered oxadiazine structure Z-8. The 1HNMR spectrum of compound Z-8 showed a mixture of lactam-lactim tautomers Z-8a and Z-8b in a 1 : 4 ratio such that two absorption singlet signals for the two methoxy protons are given besides extra exchangeable broad signals due to the OH proton for Z-8b.

The configuration assignment as the Z-isomer may be due to the downfield value of vinyl proton at δ 7.17 ppm that is more deshielded by the anisotropic effect of the carbonyl group.

The structure of oxadiazine Z-8 gets further support by its acetylation with acetic anhydride, giving the N-acetyl derivative 10 (Scheme 5).

The infrared spectrum of compound 10 does not show any absorption bands corresponding to the NH proton; instead, it exhibits broad bands at 1775 cm−1 for the two C=O groups. 1HNMR of compound 10 shows a good agreement with the proposed structure (shown in Experimental). Further support for the suggested structure gained from its mass spectra revealed the correct molecular ion peak as well as some of the important peaks (base peak).

Alkylation of compound 8 via treatment of a solution of compound 8 in acetone with ethyl chloroacetate in the presence of potassium carbonate yielded the carboxylic acid derivative 11. IR of compound 11 showed absorption bands at 3432 cm−1 for υ OH as well as the strong absorption band at 1696 cm−1 for the C=O group. Moreover, the 1HNMR spectrum displayed a singlet signal of the two methylene protons at 3.83 ppm and a broad singlet signal correlated with the COOH proton.

Also, refluxing 11 with N2H4·H2O in ethanol furnished the unexpected fused pyrazolo-oxadiazine derivative 12. The structure of compound 12 can be deduced from spectral data. The infrared spectrum was devoid of any absorption corresponding to NH and CO groups, while the 1HNMR spectrum proposed the structure of compound 12 (shown in Experimental).

The proposed pathway for the formation of compound 12 is illustrated in Scheme 6.

3. Biological Activity

The antimicrobial screening of some synthesized compounds was done using the Kirby–Bauer disc diffusion method. The possible antimicrobial activities of compounds 2, 3, 6, and 7 were investigated on four standard organisms including the Gram-positive bacteria, Staphylococcus aureus and Bacillus subtilis, and the Gram-negative bacteria, Escherichia coli, in addition to the fungus Aspergillus niger. The obtained results are presented in Table 1. Standard solutions of ciprofloxacin (Cip) and erythromycin (CN) as the antibacterial agent and amphotericin (Am) as the antifungal agent served as positive controls.

Sample no.Inhibition zone diameter (cm/gm sample)
Staphylococcus aureus G+Bacillus subtilis G+Escherichia coli G−Aspergillus niger (fungus)


Cip = ciprofloxacin (antibacterial agent); CN = erythromycin (antibacterial agent); Am = amphotericin (antifungal agent). The concentration of all synthesized compounds and the reference was 5 mg/1 ml of DMSO. Zone of inhibition: 0–16 mm = low; 14–16 mm = moderate; <16 mm = high; 0 = no inhibition.

The obtained results emphasized the fact that “chemical agent symbolized” 2 exhibited medium activity only against “Aspergillus niger (fungus)” and that compound 7 revealed low activity only against Staphylococcus aureus (Gram-positive bacterium). The compounds 6 and 3 showed medium activity against both “Staphylococcus aureus” and “Bacillus subtilis” (Gram-positive bacterium).

4. Experimental

All the melting points are uncorrected and were measured on a Gallenkamp electric melting point apparatus. The infrared spectra were recorded using potassium bromide disks on a Thermo Fisher Scientific Nicolet FTIR 7600 (USA) infrared spectrometer at the Central Laboratory of Faculty of Science, Ain Shams University. 1HNMR spectra were recorded at 300 MHz on a Gemini 300 BB NMR spectrometer using tetramethylsilane (TMS) as the internal standard in deuterated dimethylsulphoxide (DMSO-d6) at the main defense chemical laboratory. The mass spectra were recorded on a Shimadzu GCMS-QP-1000EX mass spectrometer operating at 70 eV at the Regional Center for Mycology and Biotechnology of Al-Azhar University. The elemental analyses were performed on a PerkinElmer 2400 CHN elemental analyzer at the Micro Analytical Center of Cairo University. The reactions were monitored by the thin layer chromatography on Merck Kiesel gel 60 F254 aluminum backed plates. The spots were detected by UV irradiation at 254–365 nm [18].

4.1. (Z)-4-(4-Methoxybenzylidene)-2-phenyloxazol-5(4H)-one (1)

This compound is synthesized according to the method described in [16].

4.2. 5-(4-Methoxybenzylidene)-1,2-dihydro-2,3-diphenyl-1,2,4-triazin-6(5H)-one (2)

To a solution of oxazolone 1 (0.01 mol) in acetic acid (30 ml), phenyl hydrazine (0.01 mol) and fused anhydrous sodium acetate (0.2 gm) were added. The reaction mixture refluxed for 3 hrs. The solvent was distilled under reduced pressure, and the residue was poured onto crushed ice. The solid obtained was filtered off and recrystallized from ethanol to give compound 2. Yield 60%; yellow crystals; m.p. 224–226°C (EtOH); IR (KBr) (υ, cm−1): 3248 (NH), 3066 (CHarom), 2955 (CHalkyl), 1708 (C=O), and 1638 (C=N); 1HNMR (DMSO-d6) δ: 3.98 (s, 3H, OCH3), 6.61 (s, 1H, =CH), 6.76–7.56 (m, 10H, Ar-H), 8.06 (t, 2H, Ar-H), 8.27 (d, 2H, Ar-H, J = 6.6 Hz), and 8.96 (br.s, H, NH, exchangeable); MS (70 eV) m/z (%): 369 (M+, 34), 327 (4), 262 (5), 103 (18), 91 (88), 77 (37), 65 (100), 52 (5), and 44 (10). Anal. calcd for C23H19O2N3 (396.42): C (74.78); H (5.18); and N (11.37). Found: C (74.65); H (5.07); and N (11.12).

4.3. 5-(4-Methoxybenzylidene)-6-chloro-2,5-dihydro-2,3-diphenyl-1,2,4-triazine (3)

The mixture of 2 (0.01 mol) and phosphorus pentachloride (0.01 mol) in phosphorus oxychloride (30 ml) refluxed on the water bath for 6 hrs. The reaction mixture was then poured gradually onto crashed ice. The solid obtained was filtered off and recrystallized from benzene to give compound 3. Yield 90%; pale brown crystals; m.p. 160–162°C (benzene); IR (KBr) (υ, cm−1): 3068 (CHarom), 2935 (CHalkyl), and 1600 (C=N); 1HNMR (DMSO-d6) δ: 3.72 (s, OCH3), 6.86 (s, 1H, =CH), and 7.20–7.93 (m, 14H, Ar-H); MS (70 eV) m/z (%): 387.75 (M+, 7), 356 (14), 328 (5), 235 (3), 194 (8), 104 (5), 93 (13), 77 (100), and 62 (30). Anal. calcd for C23H18ON3Cl (387.86): C (71.22); H (4.68); and N (10.83). Found: C (70.94); H (4.77); and N (10.51).

4.4. 1-(5-(4-Methoxybenzylidene)-2,5-dihydro-2,3-diphenyl-1,2,4-triazin-6-yl)hydrazine (4)

Compound 3 (0.01 mol) and hydrazine hydrate (0.01 mol) refluxed in ethyl alcohol (20 ml) for 12 hrs. A solid product obtained after cooling to room temperature was filtered off and recrystallized from ethanol to give compound 4. Yield 88%; colorless crystals; m.p. 170–172°C (EtOH); IR (KBr) (υ, cm−1): 3300, 3220 (NH, NH2), 3065 (CHarom), 2957 (CHalkyl), and 1604 (C=N); 1HNMR (DMSO-d6) δ: 3.72 (s, OCH3), 4.00 (br.s, 2H, NH2), 6.43 (s, 1H, =CH), 7.85–7.95 (m, 14H, ArH), and 8.97 (br.s, 1H, NH, exchangeable); MS (70 eV) m/z (%): 383 (M+, 2), 352 (1), 277 (5), 189 (8), 107 (8), 70 (100), 58 (2), and 44 (17). Anal. calcd for C23H21N5O (383.45): C (72.04); H (5.52); and N (18.26). Found: C (71.66); H (5.21); and N (17.95).

4.5. N′-(5-(4-Methoxybenzylidene)-2,5-dihydro-2,3-diphenyl-1,2,4-triazin-6-yl)-N-acetylacetohydrazide (5)

Solution of 4 (0.5 gm) in acetic anhydride (15 ml) was heated under reflux for 6 hrs. The solvent was distilled off under reduced pressure, and the residue was poured onto crushed ice. The solid obtained was filtered off and recrystallized to give compound 5. Yield 90%; white crystals; m.p. 108–110°C (EtOH); IR (KBr) (υ, cm−1): 3445 (NH), 3066 (CHarom), 2956, 2923, 2852 (CHalkyl), 1726, 1701 (C=O), and 1640 (C=N); 1HNMR (DMSO-d6) δ: 2.28 (s, 6H, 2CH3), 3.83 (s, 3H, OCH3), 7.00 (s, 1H, =CH), 7.07–7.92 (m, 14H, ArH), and 8.32 (br.s, 1H, NH, exchangeable); MS (70 eV) m/z (%): 467 (M+, 8), 424 (1), 368 (13), 360 (7), 352 (24), 327 (25), 273 (8), 235 (7), 194 (2), 141 (3), 91 (66), and 42 (100). Anal. calcd for C27H25N5O3 (467.52): C (69.36); H (5.39); and N (14.98). Found: C (69.12); H (5.50); and N (15.18).

4.6. Reaction of Chlorotriazine Derivative (3) with Some Nucleophilic Reagents
4.6.1. General Procedure

Compound 3 (0.01 mol) and sodium azide or anthranilic acid (0.01 mol) refluxed in acetic acid “glacial” (20 ml) for about 10–12 hrs. The solid product formed was filtered off and then recrystallized from ethanol to give compounds 6 and 7, respectively.

4.7. 8-(4-Methoxybenzylidene)-5,8-dihydro-5,6-diphenyltetrazolo[1,5-f][1,2,4]triazine (6)

Yield 75%; red crystals; m.p. 150–152°C; IR (KBr) (υ, cm−1): 3065 (CHarom), 2976, 2837 (CHalkyl), 1600 (C=N), and 1573 (N=N); 1HNMR (DMSO-d6) δ: 3.78 (s, 3H, OCH3) and 6.76–7.94 (m, 15H, ArH + CH=); MS (70 eV) m/z (%): 394 (M+, 4.5), 354 (37), 325 (2), 250 (11), 133 (5), 107 (18), 67 (4), and 48 (100). Anal. calcd for C23H18N6O (394.43): C (70.04); H (4.60); and N (21.31). Found: C (70.31); H (4.73); and N (20.90).

4.8. 4-(4-Methoxybenzylidene)-1,2-diphenyl-1H-[1,2,4]triazino[6,1-b]quinazolin-10(4H)-one (7)

Yield 80%; off-white crystals; m.p. 128–130°C; IR (KBr) (υ, cm−1): 3049 (CHarom), 2944, 2844 (CHalkyl), 1678 (C=O), and 1597 (C=N); 1HNMR (DMSO-d6) δ: 3.70 (s, OCH3), 6.42 (s, 1H, =CH), and 6.87–8.44 (m, 18H, ArH); MS (70 eV) m/z (%): 470 (M+, 7), 443 (3), 369 (6), 352 (6), 294 (15), 194 (1), 185 (3), 162 (4), 134 (3), 107 (7), 91 (64), and 43 (100). Anal. calcd for C30H22N4O2 (470.52): C (76.58); H (4.71); and N (11.91). Found: C (76.17); H (4.33); and N (11.54).

4.9. (4Z)-4-(4-Methoxybenzylidene)-6-phenyl-2H-1,2,5-oxadiazin-3(4H)-one (8)

To a solution of oxazolone 1 (0.01 mol) in pyridine (30 ml), hydroxylamine hydrochloride (0.01 mol) was added. The reaction mixture refluxed for 3 hrs. The solvent was distilled under reduced pressure, and the residue was poured onto crushed ice. The solid obtained was filtered off and recrystallized to give compound 8. Yield 53%; yellowish brown needles; m.p. 195–197°C (EtOH); IR (KBr) (υ, cm−1): 3202 (NH), 3068 (CHarom), 2962 (CHalkyl), 1700 (C=O), and 1675 (C=N); 1HNMR (DMSO-d6) δ: 7.17 (s, 1H, =CH), 6.92–8.31 (m, 18H, ArH + =CH), for Z-8a: 3.82 (s, 3H, OCH3), 9.81 (br.s, 1H, NH, exchangeable), for Z-8b: 3.75 (s, OCH3), and 11.23 (br.s, 1H, OH, exchangeable); MS (70 eV) m/z (%): 294 (M+, 37), 278 (40), 267 (1.5), 263 (1), 91 (88), 234 (1.1), 186 (6), 146 (12), 119 (16), 107 (1.3), 77 (97), 59 (15), and 40 (100). Anal. calcd for C17H14O3N2 (294.31): C (69.38); H (4.79); and N (9.52). Found: C (68.98); H (4.52); and N (9.36).

4.10. 4-(4-Methoxybenzylidene)-2-acetyl-6-phenyl-2H-1,2,5-oxadiazin-3(4H)-one (10)

A solution of 8 (0.5 gm) in acetic anhydride (20 ml) was heated under reflux for 3 hrs. The solvent was distilled off under reduced pressure, and the residue was poured onto crushed ice. The solid obtained was filtered off and recrystallized from ethanol to give compound 10. Yield 87%; yellow crystals; m.p. 124–126°C (EtOH); IR (KBr) (υ, cm−1): 3087 (CHarom), 2940, 2840 (CHalkyl), 1775, 1700 (C=O), and 1651 (C=N); 1HNMR (DMSO-d6) δ: 3.82 (s, 3H, CH3), 3.84 (s, 3H, OCH3), 7.32 (s, 1H, =CH), and 7.04–8.30 (m, 9H, ArH); MS (70 eV) m/z (%): 336 (M+, 25), 294 (1.5), 251 (21), 234 (17), 186 (47), 159 (6), 143 (100), 107 (12), and 77 (29). Anal. calcd for C19H16N2O4 (336.34): C (67.85); H (4.79); and N (8.33). Found: C (67.74); H (4.67); and N (7.95).

4.11. 2-(4-(4-Methoxybenzylidene)-6-phenyl-4H-1,2,5-oxadiazin-3-yloxy)acetic Acid (11)

A mixture of compound 8 (0.01 mol) and ethyl chloroacetate (0.01 mol) refluxed in acetone (25 ml) and potassium carbonate (0.9 gm) for 10 hrs. The solvent was distilled off under reduced pressure, and the residue was poured onto ice water. The solid product was filtered off and recrystallized from diluted ethanol to give compound 11. Yield 40%; orange crystals; m.p. 280–282°C (dil. EtOH); IR (KBr) (υ, cm−1): 3432 (OH), 3073 (CHarom), 2981, 2846 (CHalkyl), 1696 (C=O), and 1597 (C=N); 1HNMR (DMSO-d6) δ: 3.78 (s, OCH3), 3.83 (s, 2H, CH2), 6.96–8.24 (m, 9H, ArH + =CH), and 11.99 (br.s, 1H, OH, exchangeable); MS (70 eV) m/z (%): 352 (M+, 12), 334 (4.7), 294 (14), 235 (1.6), 117 (15), 77 (12), 69 (100), and 41 (34). Anal. calcd for C19H16N2O5 (352.34): C (64.77); H (4.58); and N (7.95). Found: C (64.39); H (4.32); and N (7.68).

4.12. 5-(4-Methoxyphenyl)-3-phenylpyrazolo[3,4-c][1,2,5]oxadiazine (12)

To a solution of compound 11 (0.01 mol) in ethyl alcohol (20 ml), hydrazine hydrate (0.015 mol) was added. The reaction mixture refluxed for 6 hrs. The solvent was distilled under reduced pressure, and the residue was poured onto crushed ice. The solid obtained was filtered off and recrystallized from ethanol to give compound 12. Yield: 58%; pink needles; m.p. 155–157°C (EtOH); IR (KBr) (υ, cm−1): 3015 (CHarom), 2937, 2844 (CHalkyl), and 1606 (C=N); 1HNMR (DMSO-d6) δ: 3.81 (s, OCH3) and 7.02–8.61 (m, 10H, ArH + =CH); MS (70 eV) m/z (%): 304 (M+, 8), 276 (6), 227 (1), 195 (1.4), 185 (3), 119 (9), 107 (8), 91 (10), 77 (79), 70 (23), 57 (100), and 54 (12). Anal. calcd for C17H12N4O2 (304.30): C (67.10); H (3.97); and N (18.41). Found: C (66.72); H (4.25); and N (18.12).

Data Availability

The instrumental data including IR, mass, HNMR, and elemental analysis data used to support the findings of this study are included within the article.

Conflicts of Interest

The authors declare that they have no conflicts of interest.


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Copyright © 2019 Heba E. Hashem and Ahmed M. Abo-Bakr. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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