Journal of Chemistry

Journal of Chemistry / 2017 / Article

Research Article | Open Access

Volume 2017 |Article ID 2384780 |

Fernando Rocha-Alonzo, Daniel Chávez, Adrián Ochoa-Terán, David Morales-Morales, Enrique F. Velázquez-Contreras, Miguel Parra-Hake, "A Novel Synthesis of 1,2,3-Benzotriazinones from 2-(o-Aminophenyl)oxazolines", Journal of Chemistry, vol. 2017, Article ID 2384780, 5 pages, 2017.

A Novel Synthesis of 1,2,3-Benzotriazinones from 2-(o-Aminophenyl)oxazolines

Academic Editor: Hakan Arslan
Received29 Sep 2016
Accepted13 Dec 2016
Published19 Jan 2017


1,2,3-Benzotriazinones were synthesized in excellent yields by the reaction of 2-(o-aminophenyl)oxazolines and isoamyl nitrite in methanol. The crystal structure of the acetyl derivative of one of the 1,2,3-benzotriazinones provided additional support for the spectroscopic structural characterization of the title compounds.

1. Introduction

1,2,3-Benzotriazinones are compounds widely investigated due to their interesting biological and chemical properties. These heterocyclic compounds have been studied as anaesthetic [1], anti-inflammatory [2], anticancer [3, 4], and antitumoral [5, 6] agents. In organic synthesis, triazinones are used as an activating moiety in coupling agents for the preparation of peptides and amino acids [79]. As a result of their biological and synthetic importance, there is still interest in the development of methods for the synthesis of compounds which contain the 1,2,3-triazinone moiety.

In general, 1,2,3-benzotriazinones are prepared via intramolecular cyclization through diazonium ion condensation with an adjacent nucleophilic function. Using this strategy, 1,2,3-triazinones have been obtained from aminobenzamides [1012], aminonitriles [13, 14], and triazenes [1517]. Other workers have reported the synthesis of 1,2,3-benzotriazinones by the oxidation of indazol-3-amines with hydrogen peroxide in the presence of sodium carbonate, though in low yields, and by the cyclization of 2-azido-N-4-toluoylbenzamide in moderate yields [18].

In this report, we describe facile access to the title compounds from chiral and nonchiral 2-(o-aminophenyl)oxazolines. Since racemization is not possible during the reaction, this method allows the preparation of enantiopure 1,2,3-benzotriazinones in excellent yields.

2. Results and Discussion

The first step for the synthesis of 1,2,3-benzotriazinones was the preparation of 2-(o-aminophenyl)oxazolines 3a3c (see (1)). These oxazolines were prepared in high yields (58–80%) by cyclization of anthranilonitrile with ethanolamines under basic conditions in a mixture of glycerol and ethylene glycol, following the methodology reported by Gómez and coworkers [19]. In the literature, it has been reported that oxazolines 3a and 3b were obtained as oils, whereas in our work both were isolated as solids; we believe this fact is due to problems in the purification process in the previous report. Nevertheless, NMR and IR spectroscopic and mass spectrometry data are consistent with those previously reported [20].

Once the necessary 2-(o-aminophenyl)oxazolines were obtained, the next step was the synthesis of the 1,2,3-benzotriazinones 4a4c. Compounds 4a4c were synthesized by diazotization reaction involving oxazolines 3a3c and methanolic isoamyl nitrite. In all cases, the new 1,2,3-benzotriazinones were obtained in quantitative yields (Scheme 1).

It is assumed that the reaction takes place by the intermediacy of the diazonium ion 5 formed from 2-(o-aminophenyl)oxazoline (3) using a large excess of isoamyl nitrite in order to ensure formation of the diazonium salt (Scheme 1). The electron withdrawing effect of the diazonium group in 5 could promote oxazolinyl ring hydrolysis, taking water from the alcoholic media, and producing the 2-carbamoylbenzenediazonium 6. The 1,2,3-triazinone moiety in 4 is then achieved by ring closure between the amide and the adjacent diazonium group in 6. Similar mechanistic assumptions were proposed by Colomer and Moyano in the synthesis of this kind of compound from aminonitriles [13, 21].

Infrared spectroscopy of compounds 4a4c showed a single band at ca. (ν) 3430 cm−1 due to the O-H stretching; the bands at ca. (ν) 1687 cm−1 and at ca. (ν) 1657 cm−1 correspond to the N=N and the C=O stretching, respectively. 1H NMR spectroscopy showed the following: aromatic hydrogen from the 1,2,3-benzotriazinone moiety appeared as an ABCD system with the characteristic two doublets and two triplets between 8.29 and 7.87 ppm, slightly shifted to lower field relative to the 2-(o-aminophenyl)oxazolines; aliphatic protons appeared between 6.39 and 0.90 ppm. For compound 4b, the phenyl protons are at (δ) 7.43 ppm. 13C NMR spectroscopy showed carbonyl carbon at ca. (δ) 156.5 ppm; aromatic carbon appeared in the range 146.1–120.3 ppm and aliphatic carbon in the range 64.2–10.8 ppm. The proton of hydroxyl group in the proposed structure was not identified by 1H NMR, but the carbinol moiety was inferred from the chemical shifts on 13C NMR data. Since compounds 4a4c are novel, high-resolution mass spectrometry was run with no significant difference between calculated and obtained values (less than ±0.003 amu). In general, the molecular formula assignment and the spectroscopic characterization were consistent with their structures.

In order to corroborate the presence of the hydroxyl group, the acetyl derivative 7a was obtained by reaction of 4a with acetic anhydride in pyridine (see (2)). NMR spectra for the acetyl derivative 7a turned out to be similar to 4a, but with new signals for the acetyl moiety at 1.95 and 21.5 for the methyl group and 171.9 for the ester carbonyl.

Suitable crystals for X-ray diffraction studies of 1,2,3-benzotriazinone 7a were grown by slow vapor diffusion of hexane into a saturated solution in ethyl acetate. Compound 7a crystallized in the triclinic system with the space group Pī. Molecular structure of 1,2,3-benzotriazinone 7a is shown in Figure 1, which confirms the presence of the 1,2,3-triazinone system and indirectly corroborates the hydroxyl group in 1,2,3-benzotriazinones 4a4c.

In the molecular structure of 7a, the N1=N2 bond [1.2715(19) Å] is longer than the typical value for N=N double bond (1.236 Å) [22], whereas the N2-N3 bond [1.3728(19) Å] is slightly shorter than the typical value for N-N single bond (1.404 Å) [22]. The structure shows coplanarity between the two rings. These data are in agreement with crystal structure reports of related 1,2,3-benzotriazinones [17, 2325]. Crystallographic data of 7a are included as supplementary material (in Supplementary Material available online at

Of interest to pharmaceutical applications, Reingruber et al. have suggested that the coplanar structure in 1,2,3-benzotriazinones could have DNA-intercalating abilities such as those displayed by some anticancer agents [17].

In summary, we have presented an efficient method for the synthesis of 1,2,3-benzotriazinones from 2-(o-aminophenyl)oxazolines in high yields.

3. Experimental Section

3.1. General Procedures

All reagents were purchased in the highest quality available and were used without further purification. The solvents used in column chromatography were obtained from commercial suppliers and used without distillation. Infrared spectra (FTIR) were recorded on a Perkin Elmer FT-IR 1600 spectrophotometer. Nuclear magnetic resonance 1H (at 200 MHz) and 13C (at 50 MHz) spectra were recorded on a Varian Mercury 200 MHz spectrometer in (CD3)2CO with TMS as internal standard. Melting points were obtained on an Electrothermal 88629 apparatus. Optical rotations were determined using an Autopol III polarimeter. EIMS were recorded on an Agilent Technologies 5975C mass spectrometer. The ESI-HRMS data were performed at High-Resolution Mass Spectrometry Facility, UC Riverside.

3.2. General Procedure for the Synthesis of 2-(o-Aminophenyl)Oxazoline (3)

Anthranilonitrile (1 equiv.), potassium carbonate (0.1 equiv.), and ethanolamine (1.7 equiv.) were placed in a Schlenk flask, followed by a solution of glycerol in dry ethylene glycol (5 : 9) (3.3 mL of solution per mmol of anthranilonitrile). The resulting mixture was stirred at 105°C under argon until the disappearance of the nitrile (followed by TLC, hexane/ethyl acetate, 3 : 1). The mixture was cooled to room temperature and then poured over crushed ice. The resulting white solid was filtered and then dissolved in dichloromethane. The organic solution was washed with water, dried over anhydrous Na2SO4, and filtered, and the solvent was evaporated under reduced pressure to give a crude product that was purified by flash chromatography on neutral alumina (hexane/ethyl acetate, 20 : 1) to give the pure product.

2-[4,5-Dihydro-1,3-oxazol-2-yl]aniline (3a). White solid (58% yield), mp 52-53°C. FTIR (KBr): ν 3384, 3264, 1630, 1254 cm−1. 1H NMR [(CD3)2CO, 200 MHz]: 7.69 (dd, = 7.9, 1.7 Hz, 1H), 7.19 (ddd, , 7.1, 1.6 Hz, 1H), 6.66 (m, 2H), 6.04 (s, 2H), 4.30 (m, 2H), 4.08 (m, 2H). 13C NMR [(CD3)2CO, 50 MHz]: 164.4, 148.1, 131.6, 129.3, 115.7, 115.4, 108.9, 65.6, 54.8. EI-MS (Int. %): [M]+ 162 (100), 131 (36), 118 (33).

2-[(4R)-4-Phenyl-4,5-dihydro-1,3-oxazol-2-yl]aniline (3b). Yellow solid (72% yield), mp 62-63°C. (c 0.22, MeOH). FTIR (KBr): ν 3416, 3272, 1631, 1249 cm−1. 1H NMR [(CD3)2CO, 200 MHz]: 7.70 (dd, , 1.8 Hz, 1H), 7.32 (m, 5H), 7.21 (ddd, , 7.0, 1.4 Hz, 1H), 6.83 (dd, , 0.8 Hz, 1H), 6.80 (br. s, 2H), 6.60 (ddd, , 7.0, 1.2 Hz, 1H), 5.43 (dd, , 8.2 Hz, 1H), 4.66 (dd, , 8.3 Hz, 1H), 4.11 (dd, , 8.2 Hz, 1H). 13C NMR [(CD3)2CO, 50 MHz]: 165.0, 148.8, 142.7, 132.3, 129.8, 128.7, 127.5, 126.6, 116.0, 115.7, 108.6, 73.0, 70.2. EI-MS (Int. %): [M]+ 238 (100), 207 (48), 118 (50).

2-[(4R)-4-Ethyl-4,5-dihydro-1,3-oxazol-2-yl]aniline (3c). Brown oil (80% yield). (c 0.22, MeOH). FTIR (NaCl): ν 3461, 3286, 1632, 1263 cm−1. 1H NMR [(CD3)2CO, 200 MHz]: 7.62 (dd, , 1.6 Hz, 1H), 7.15 (ddd, , 6.0, 2.0 Hz, 1H), 6.77 (dd, , 0.7 Hz, 1H), 6.74 (br. s, 2H), 6.55 (ddd, , 7.0, 1.2 Hz, 1H), 4.28 (m, 2H), 3.90 (m, 1H), 1.59 (m, 2H), 0.97 (t, , 3H). 13C NMR [(CD3)2CO, 50 MHz]: 164.1, 150.3, 132.4, 130, 116.1, 115.4, 109, 70.8, 68.8, 29.5, 10.4. EI-MS (Int. %): [M]+ 190 (81), 161 (100), 133 (59), 118 (31).

3.3. General Procedure for the Synthesis of 1,2,3-Benzotriazinones

To a solution of 2-(o-aminophenyl)oxazoline (3) (1 equiv.) in methanol, a solution of isoamyl nitrite (8 equiv.) in methanol was added. The reaction mixture was stirred at room temperature until the disappearance of the aniline (followed by TLC, hexane/ethyl acetate, 3 : 1). The solvent was evaporated under reduced pressure to give a crude product that was purified by washing with petroleum ether and recrystallization from hexane/ethyl acetate.

3-(2-Hydroxyethyl)-1,2,3-benzotriazin-4(3H)-one (4a). White solid (>99% yield), mp 111-112°C. FTIR (KBr): ν 3431, 1691, 1646, 1300 cm−1. 1H NMR [(CD3)2CO, 200 MHz]: 8.29 (ddd, , 1.5, 0.7 Hz, 1H), 8.15 (ddd, , 1.5, 0.6 Hz, 1H), 8.06 (ddd, , 7.0, 1.5 Hz, 1H), 7.91 (ddd, , 6.9, 1.6 Hz, 1H), 4.57 (t, , 2H), 4.02 (t, , 2H). 13C NMR [(CD3)2CO, 50 MHz]: 157.1, 146.1, 136.8, 134.2, 129.8, 126.5, 121.7, 61.2, 54.1. ESI-HRMS: 192.0778 (100), calculated for [M+H]+, C9H10N3O2, 192.0768.

3-((R)-2-Hydroxy-1-phenylethyl)-1,2,3-benzotriazin-4(3H)-one (4b). White solid (>99% yield), mp 79-80°C. (c 0.22, MeOH). FTIR (KBr): ν 3419, 1683, 1661, 1294 cm−1. 1H NMR [(CD3)2CO, 200 MHz]: 8.27 (ddd, , 1.5, 0.6 Hz, 1H), 8.16 (ddd, , 1.3, 0.6 Hz, 1H), 8.04 (ddd, , 7.1, 1.5 Hz, 1H), 7.87 (ddd, , 7.1, 1.3 Hz, 1H), 7.43 (m, 5H), 6.39 (dd, , 5.2 Hz, 1H), 4.70 (dd, , 9.7 Hz, 1H), 4.25 (dd, , 5.2 Hz, 1H). 13C NMR [(CD3)2CO, 50 MHz]: 156.1, 144.6, 138.6, 136.0, 133.3, 129.4, 128.9, 128.9, 128.7, 125.7, 120.5, 64.0, 63.3. ESI-HRMS: 268.1094 (100), calculated for [M+H]+, C15H14N3O2, 268.1081.

3-((R)-1-Hydroxybutan-2-yl)-1,2,3-benzotriazin-4(3H)-one (4c). White solid (>99% yield), mp 89-90°C. (c 0.22, MeOH). FTIR (KBr): ν 3439, 1686, 1663, 1296 cm−1. 1H NMR [(CD3)2CO, 200 MHz]: 8.29 (ddd, , 1.5, 0.6 Hz, 1H), 8.16 (ddd, , 1.5, 0.6 Hz, 1H), 8.07 (ddd, , 7.0, 1.5 Hz, 1H), 7.91 (ddd,, , 7.0, 1.5 Hz, 1H), 5.22 (m, 1H), 4.10 (dd, , 8.4 Hz, 1H), 3.96 (dd, , 5.1 Hz, 1H), 1.99 (quin, , 2H), 0.90 (t, , 3H). 13C NMR [(CD3)2CO, 50 MHz]: 156.6, 144.5, 135.8, 133.2, 128.8, 125.7, 120.3, 64.2, 62.3, 24.2, 10.8. ESI-HRMS: 220.1091 (100), calculated for [M+H]+, C11H14N3O2, 220.1081.

3.4. Procedure for the Synthesis of Acetylated Derivative 3-(2-Hydroxyethyl)-1,2,3-benzotriazin-4(3H)-onyl Acetate (7a)

To a solution of 1,2,3-benzotriazinone (4a) (200 mg, 1.0 mmol in 3.0 mL pyridine), excess of acetic anhydride (3.0 mL, 32 mmol) was added. The reaction mixture was stirred at room temperature for 24 h. To purify the acetylated derivative 7a, sodium hydroxide (2.6 g, 64 mmol in 30 mL of water) was added to the reaction mixture and then extracted with ethyl acetate (3 × 10 mL). The organic phase was washed with 2 M HCl (3 × 40 mL), dried over anhydrous sodium sulfate, and filtered. The solvent was evaporated under reduced pressure and the white solid dried in vacuum for 24 h.

A white solid was obtained (240 mg, 1.0 mmol, quantitative yield). FTIR (KBr): ν 3072, 1741, 1685, 1230 cm−1. 1H NMR [(CD3)2CO, 200 MHz]: 8.30 (ddd, , 1.5, 0.6 Hz), 8.17 (ddd, , 1.6, 0.6 Hz), 8.09 (ddd, , 7.0, 1.5 Hz), 7.93 (ddd, , 6.9, 1.6 Hz), 4.70 (t, , 2H), 4.55 (t, , 2H), 1.95 (s, 3H). 13C NMR [(CD3)2CO, 50 MHz]: 171.9, 157.0, 146.0, 136.9, 134.4, 130.0, 126.5, 121.6, 63.0, 50.4, 21.5.

X-Ray Data Collection and Refinement. The details of the structure determination are given in Table , atomic coordinates are given in Table , and bond lengths (Å) and angles (°) are given in Table in Supporting Information. Crystallographic data for the structural analyses have been deposited with the Cambridge Crystallographic Data Centre CCDC 903418. Further details of the crystal structure investigation are available free of charge via (or from the CCDC, 12 Union Road, Cambridge CB2 1EZ, UK; fax: +44 1223 336033; e-mail:

Competing Interests

The authors declare that there are no competing interests regarding the publication of this paper.


The authors gratefully acknowledge support from Consejo Nacional de Ciencia y Tecnología (CONACyT Grant 36435-E and “Supramolecular Chemistry Thematic Network” Grant 271884), Programa de Mejoramiento del Profesorado (Apoyo a la Incorporación de Nuevos PTC Grant Promep/103.5/11/4462), and Consejo del Sistema Nacional de Educación Tecnológica (COSNET, Grant 486-02-P). The authors are indebted to Ignacio Rivero Espejel and Ratnasamy Somanathan for their support in this work.

Supplementary Materials

Supporting Information contains crystal data and structure refinement for the 1,2,3-benzotriazinone 7a. The details of structure determination include atomic coordinates, bond lengths and angles.

  1. Supplementary Material


  1. G. Caliendo, F. Fiorino, P. Grieco et al., “Preparation and local anaesthetic activity of benzotriazinone and benzoyltriazole derivatives,” European Journal of Medicinal Chemistry, vol. 34, no. 12, pp. 1043–1051, 1999. View at: Publisher Site | Google Scholar
  2. G. Z. Zheng, P. Bhatia, J. Daanen et al., “Structure-activity relationship of triazafluorenone derivatives as potent and selective mGluR1 antagonists,” Journal of Medicinal Chemistry, vol. 48, no. 23, pp. 7374–7388, 2005. View at: Publisher Site | Google Scholar
  3. A. Vaisburg, N. Bernstein, S. Frechette et al., “(2-Amino-phenyl)-amides of ω-substituted alkanoic acids as new histone deacetylase inhibitors,” Bioorganic & Medicinal Chemistry Letters, vol. 14, no. 1, pp. 283–287, 2004. View at: Publisher Site | Google Scholar
  4. A.-M. Chollet, T. Le Diguarher, N. Kucharczyk et al., “Solid-phase synthesis of α-substituted 3-bisarylthio N-hydroxy propionamides as specific MMP inhibitors,” Bioorganic & Medicinal Chemistry, vol. 10, no. 3, pp. 531–544, 2002. View at: Publisher Site | Google Scholar
  5. T. Le Diguarher, A.-M. Chollet, M. Bertrand et al., “Stereospecific synthesis of 5-substituted 2-bisarylthiocyclopentane carboxylic acids as specific matrix metalloproteinase inhibitors,” Journal of Medicinal Chemistry, vol. 46, no. 18, pp. 3840–3852, 2003. View at: Publisher Site | Google Scholar
  6. A. S. Clark, B. Deans, M. F. G. Stevens et al., “Antitumor imidazotetrazines. 32. Synthesis of novel imidazotetrazinones and related bicyclic heterocycles to probe the mode of action of the antitumor drug temozolomide,” Journal of Medicinal Chemistry, vol. 38, no. 9, pp. 1493–1504, 1995. View at: Publisher Site | Google Scholar
  7. L. A. Carpino, J. Xia, C. Zhang, and A. El-Faham, “Organophosphorus and nitro-substituted sulfonate esters of 1-hydroxy-7-azabenzotriazole as highly efficient fast-acting peptide coupling reagents,” Journal of Organic Chemistry, vol. 69, no. 1, pp. 62–71, 2004. View at: Publisher Site | Google Scholar
  8. V. Janout, B. Jing, I. V. Staina, and S. L. Regen, “Selective transport of ATP across a phospholipid bilayer by a molecular umbrella,” Journal of the American Chemical Society, vol. 125, no. 15, pp. 4436–4437, 2003. View at: Publisher Site | Google Scholar
  9. T. M. Gierasch, M. Chytil, M. T. Didiuk et al., “A modular synthetic approach toward exhaustively stereodiversified ligand libraries,” Organic Letters, vol. 2, no. 25, pp. 3999–4001, 2000. View at: Publisher Site | Google Scholar
  10. T. Okuzumi, E. Nakanishi, T. Tsuji, and S. Makino, “Efficient solid-phase synthesis of diverse 1,2,3-benzotriazin-4-ones using tert-butyl nitrite,” Tetrahedron Letters, vol. 44, no. 29, pp. 5539–5542, 2003. View at: Publisher Site | Google Scholar
  11. A. Deeb, M. Kotb, and M. El-Abbasy, “Pyridazine derivatives and related compounds, part 12: synthesis of some pyridazino [4′,3′:4,5]thieno[3,2-d]-1,2,3-triazines,” Phosphorus, Sulfur, and Silicon and the Related Elements, vol. 180, no. 2, pp. 591–599, 2005. View at: Publisher Site | Google Scholar
  12. K. M. Dawood, A. M. Farag, and N. A. Khedr, “Facile route to novel 2-pyridone, pyrazolo[3,4-d]-1,2,3-triazine, and pyrazolo[3,4-d]- and [1,5-a]-pyrimidine derivatives,” Arkivoc, vol. 2008, no. 15, pp. 166–175, 2008. View at: Publisher Site | Google Scholar
  13. J. P. Colomer and E. L. Moyano, “New application of heterocyclic diazonium salts. Synthesis of pyrazolo[3,4-d][1,2,3]triazin-4-ones and imidazo[4,5-d][1,2,3]triazin-4-ones,” Tetrahedron Letters, vol. 52, no. 14, pp. 1561–1565, 2011. View at: Publisher Site | Google Scholar
  14. M. Tišler and B. Stanovnik, “Heterocyclic diazo compounds as starting materials in organic synthesis (review),” Chemistry of Heterocyclic Compounds, vol. 16, no. 5, pp. 443–463, 1980. View at: Publisher Site | Google Scholar
  15. C. Gil and S. Bräse, “Solid-phase synthesis of biologically active benzoannelated nitrogen heterocycles: an update,” Journal of Combinatorial Chemistry, vol. 11, no. 2, pp. 175–197, 2009. View at: Publisher Site | Google Scholar
  16. C. Gil, A. Schwögler, and S. Bräse, “The Synthesis of 3-Substituted 6-Aryl-3 H-benzo[a][1,2,3]triazinones Using Polymer-Bound Triazenes,” Journal of Combinatorial Chemistry, vol. 6, no. 1, pp. 38–42, 2004. View at: Publisher Site | Google Scholar
  17. R. Reingruber, S. Vanderheiden, T. Muller, M. Nieger, M. Es-Sayed, and S. Bräse, “Efficient synthesis of substituted 3-acyl-3,4-dihydrobenzo[d][1,2,3]triazines,” Tetrahedron Letters, vol. 50, no. 26, pp. 3439–3442, 2009. View at: Publisher Site | Google Scholar
  18. H. Döpp and D. Döpp, “Product class 2: six-membered hetarenes with three heteroatoms,” in Science of Synthesis, Chapter 17: Category 2, Hetarenes and Related Ring Systems, 2004. View at: Publisher Site | Google Scholar
  19. M. Gómez, S. Jansat, G. Muller, G. Aullón, and M. A. Maestro, “Ruthenium complexes containing chiral N-donor ligands as catalysts in acetophenone hydrogen transfer—new amino effect on enantioselectivity,” European Journal of Inorganic Chemistry, vol. 2005, no. 21, pp. 4341–4351, 2005. View at: Publisher Site | Google Scholar
  20. A. S. Gajare, N. S. Shaikh, G. K. Jnaneshwara, V. H. Deshpande, T. Ravindranathan, and A. V. Bedekar, “Clay catalyzed conversion of isatoic anhydride to 2-(o-aminophenyl)oxazolines,” Journal of the Chemical Society, Perkin Transactions 1, no. 6, pp. 999–1001, 2000. View at: Publisher Site | Google Scholar
  21. E. L. Moyano, J. P. Colomer, and G. I. Yranzo, “New application of heterocyclic diazonium salts: synthesis of new pyrazolo[3,4-d][1,2,3]triazin-4-ones,” European Journal of Organic Chemistry, vol. 2008, no. 19, pp. 3377–3381, 2008. View at: Publisher Site | Google Scholar
  22. F. H. Allen, O. Kennard, D. G. Watson, L. Brammer, A. G. Orpen, and R. Taylor, “Tables of bond lengths determined by x-ray and neutron diffraction. Part 1. Bond lengths in organic compounds,” Journal of the Chemical Society, Perkin Transactions 2, no. 12, pp. S1–S19, 1987. View at: Google Scholar
  23. W. E. Hunt, C. H. Schwalbe, and K. Vaughan, “3-Hydroxy-1,2,3-benzotriazin-4(3H)-one, C7H5N3O2,” Acta Crystallographica Section C, vol. 39, no. 6, pp. 738–740, 1983. View at: Publisher Site | Google Scholar
  24. J. Hjortås, “The crystal and molecular structure of 1,2,3-benzotriazin-4(3H)-one,” Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry, vol. 29, no. 9, pp. 1916–1922, 1973. View at: Publisher Site | Google Scholar
  25. F. Rocha-Alonzo, G. Aguirre, and M. Parra-Hake, “N-(2-Hydroxy-ethyl)-2-[3-(p-tol-yl)triazen-1-yl]benzamide,” Acta Crystallographica Section E, vol. 65, no. 5, pp. o990–o991, 2009. View at: Publisher Site | Google Scholar

Copyright © 2017 Fernando Rocha-Alonzo et al. 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.

Related articles

No related content is available yet for this article.
 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

No related content is available yet for this article.

Article of the Year Award: Outstanding research contributions of 2021, as selected by our Chief Editors. Read the winning articles.