Vashundhra Sharma1†
Pradeep K. Jaiswal1†
Mukesh Saran2
Dharmendra Kumar Yadav3*
Saloni3
Manas Mathur2
Ajit K. Swami2Sanjeev Misra4Mi-hyun Kim3
Sandeep Chaudhary1*- 1Laboratory of Organic and Medicinal Chemistry, Department of Chemistry, Malaviya National Institute of Technology, Jaipur, India
- 2Department of Advance Molecular Microbiology, Seminal Applied Sciences Pvt. Ltd., Jaipur, India
- 3College of Pharmacy, Gachon University of Medicine and Science, Incheon, South Korea
- 4Department of Biochemistry, All India Institute of Medical Sciences (AIIMS), Jodhpur, India
The discovery of C-3 tethered 2-oxo-benzo[1,4]oxazines as potent antioxidants is disclosed. All the analogs 20a-20ab have been synthesized via “on water” ultrasound-assisted irradiation conditions in excellent yields (upto 98%). All the compounds have been evaluated for their in vitro antioxidant activities using DPPH free radical scavenging assay as well as FRAP assay. The result showed promising antioxidant activities having IC50 values in the range of 4.74 ± 0.08 to 92.20 ± 1.54 μg/mL taking ascorbic acid (IC50 = 4.57 μg/mL) as standard reference. In this study, compounds 20b and 20t, the most active compound of the series, showed IC50 values of 6.89 ± 0.07 μg/mL and 4.74 ± 0.08 μg/mL, respectively in comparison with ascorbic acid. In addition, the detailed SAR study shows that electron-withdrawing group increases antioxidant activity and vice versa. Furthermore, in the FRAP assay, eight compounds (20c, 20j, 20m, 20n, 20r, 20u, 20z, and 20aa) were found more potent than standard reference BHT (C0.5FRAP = 546.0 ± 13.6 μM). The preliminary cytotoxic study reveals the non-toxic nature of active compounds 20b and 20t in non-cancerous 3T3 fibroblast cell lines in MTT assay up to 250 μg/mL concentration. The results were validated via carrying out in silico molecular docking studies of promising compounds 20a, 20b, and 20t in comparison with standard reference. To the best of our knowledge, this is the first detailed study of C-3 tethered 2-oxo-benzo[1,4]oxazines as potential antioxidant agents.
Introduction
“Antioxidant” are primarily reducing agents/compounds which refer to the activity of numerous vitamins, minerals and phytochemicals (such as vitamin E, vitamin C and glutathione etc.) by providing protection against the damage caused by reactive oxygen species (ROS) (Park and Pezzutto, 2002; Trombino et al., 2004; Govindarajan et al., 2005; Zhang et al., 2006). Antioxidants (either natural or synthetic) are molecules, which are capable of neutralizing free radicals as well as ROS by acting at several levels such as: prevention, interception, and repair (Lehtinen and Bonni, 2006; Khan et al., 2011; Bayoumi and Elsayed, 2012). Thus, the search for antioxidants has been stimulated due to their significant importance in human health (Balakin et al., 2004; Mitra et al., 2009). Moreover, it is known that ROS like superoxides (), peroxyls (ROO−), hydroxyls (HO−), alkoxyls (RO−), nitric oxides (NO−), play a important role in disturbing metabolic pathways associated with several pathological conditions, such as cardiovascular diseases, metabolic disorders, and even carcinogenesis (Lai et al., 2001; Cheng et al., 2011). Therefore, the human body is capable to neutralize ROS by antioxidant defense mechanisms by eradicating an excess of ROS from the cell (Apel and Hirt, 2004; Zhang et al., 2010; Mittal et al., 2014). An imbalances between the detoxification of ROS with respect to their production leads to a phenomena known as “oxidative stress (OS)” which is correlated to several diseases such as stroke (Simao et al., 2015), myocardial infarction (Hassan et al., 2015), cancer (Aldawsari et al., 2016), Parkinson's disease (Wood-Kaczmar et al., 2006) and Alzheimer's disease (Nunomura et al., 2006). Therefore, the development of natural as well as synthetic antioxidants, which are able to scavenge ROS and keep cell integrity via prevention or reduction of the impact of OS on cells, is now currently an recognized area of research interest.
During the last decade, benzoxazines, benzodioxine, and its derivatives have emerged as a possible antioxidants (Largeron et al., 1999, 2001; Czompa et al., 2000; Sadiq et al., 2015). Several naturally occurring antioxidants (Abdel-lateif et al., 2016; Aziz and Karboune, 2016) such as dimboa 1 (Niemeyer, 2009; Adhikari et al., 2013; Glenska et al., 2015) and sylbin 2 (Kosina et al., 2002; Varga et al., 2006; Surai, 2015; Vavríkova et al., 2017) have been identified as promising antioxidant agents. Likewise, several synthetic molecules bearing benzoxazines as whole or as part in their structure, have also been identified as potential antioxidant agents such as exifone 3 (Largeron et al., 1995; Largeron and Fleury, 1998), isatoic anhydrides i.e., benzoxazine-2,4-diones 4 (Sáncheza et al., 2014), 2-hydroxy-1,4-benzoxazin-3(4H)-one 5 (Harput et al., 2011), and some analogs 6a-b (Largeron et al., 1999) etc. as shown in Figure 1. This encourages us to synthesize non-naturally occurring benzo [1,4] oxazines analogs.
Figure 1. Structures of some natural as well as synthetic compounds (1-6) having antioxidant activity.
Moreover, several natural products like Curcumine 7 (Barclay and Vinqvist, 2000), Quinolines 8 (Detsi et al., 2007; Savegnago et al., 2013; Oliveri et al., 2015), Chalcones 9 (Qian et al., 2011; Shakil et al., 2013; El Sayed Aly et al., 2014), Resveratrol 10 (Scartezzini and Speroni, 2000), Rosmarinic acid 11 (Fadel et al., 2011; Zhu et al., 2014), Trolox 12 (Hall et al., 2010a), Coumarins-chalcone hybrid 13 (PérezCruz et al., 2013; Mazzone et al., 2016), and Quercetin 14 (Kumar et al., 2007) etc. were also reported as antioxidants. However, due to several drawbacks such as poor solubility, less abundance and severe toxicity; their antioxidant properties were found to be relatively lower. Thus, there is still an urgent need to develop a potent antioxidant by designing a new scaffold via structural modification and incorporation of functional group present in these antioxidants. Hence, based on above fact, we have designed prototype 15 i.e., C-3 tethered 2-oxo-benzo[1,4]oxazine, incorporating similar sub-structural units assuming that the resulting structure will be a new class of potent antioxidant agent (Figure 2).
Figure 2. Design strategy for the target compound 2-oxo-benzo[1,4]oxazine 15 as an antioxidants.
In the continuation toward the search of new class of antioxidants; we were interested to explore the designed prototype 15. Therefore herein, we report the synthesis via our methodology (Jaiswal et al., 2017), antioxidant activity, and SAR of a series of C-3 tethered 2-oxo-benzo[1,4]oxazine analogs 20a-20ab. Although compounds 20a-i, 20l, 20t-w, 20y, and 20aa-ab have been earlier reported in the literature but were prepared by other routes (Iwanami et al., 1971; Mashevskaya et al., 2002; Gein et al., 2008; Xia, 2008; Xia et al., 2008; Stepanova et al., 2011, 2013; Maslivets and Maslivets, 2012). Moreover, their antioxidant activities are also not reported so far in the literature. To the best of our knowledge, the antioxidant activities of all the synthesized compounds 20a-20ab, were evaluated for the first time using DPPH radical scavenging assay taking ascorbic acid as standard reference and FRAP assay using BHT as standard reference. In addition, the cytotoxic studies of active compounds were also performed. Moreover, we also report the validation of our results via in silico molecular docking studies of compounds 20a, 20b and 20t in comparison with standard reference ascorbic acid.
Materials and Methods
General Experimental
All glass apparatus were oven dried prior to use. Melting points were taken in open capillaries on complab melting point apparatus and are presented uncorrected. Ultrasonic irradiation was performed in a Elmasonic S 30 (H) ultrasonic water bath cleaner and the reaction vessel was positioned in the maximum energy area in the cleaner and the removal or addition of water was used to control the temperature of the water bath. Infrared spectra were recorded on a Perkin-Elmer FT-IR Spectrum 2 spectrophotometer 1H NMR and 13C NMR spectra were recorded on ECS 400 MHz (JEOL) NMR spectrometer using CDCl3, CD3ODandCD3SOCD3 as solvent and tetramethylsilane as internal reference. Electrospray ionization mass spectrometry (ESI-MS) and HRMS were recorded on Xevo G2-S Q Tof (Waters, USA) Spectrometer. Column chromatography was performed over Merck silica gel (particle size: 60-120 Mesh) procured from Qualigens? (India), flash silica gel (particle size: 230-400 Mesh). All chemicals and reagents were obtained from Sigma Aldrich (USA), Merck (India) or Spectrochem (India) and were used without further purification.
General Procedure for the Synthesis of Functionalized Diketo-Acid 18a-h
Substituted acetophenone 16a-h (2.00 mmol, 1eq.) were taken in toluene (50 ml) and NaH (2.20 mmol, 1.1 eq.) was added carefully. After stirring this reaction mixture at 0°C for 30 min dimethyl oxalate (2.20 mmol, 1.1 eq.) were added and reflux for 6 h. The progresses of the reaction were monitored by TLC using 9:1 Hexane/ethyl acetate as an eluent. After completion of reaction, the reaction mixture was quenched with distilled water and extracted with ethyl acetate (3 × 50 ml); then with distilled water (2 × 10 mL) followed by brine solution (2 × 20 mL). The organic layer was combined and dried over anhydrous Na2SO4 and the organic solvent was removed under reduced pressure to give the crude product. The crude products were purified by recrystalization using EtOAc/Hexane (v/v = 20:80), which afforded the pure desired diketo-ester 17a-h in 78-92% yields. Compounds 17a-h was used for next step without any further purification.
To a solution of 17a-h (1.00 mmol, 1eq.) in MeOH:THF: H2O (10 ml, 7:2:1), added LiOH.H2O (1.20 mmol, 1.2eq) into the reaction mixture and stirred it for 4 h at room temperature. The progress of the reaction was monitored by TLC. After completion of the reaction, it was quenched with 3N HCl solution and extracted with ethyl acetate (3 × 30 mL); then with distilled water (2 × 10 mL) followed by brine solution (2 × 20 mL). The combined organic layer was dried over anhydrous Na2SO4 and evaporated under vacuum to afford the corresponding crude product. These crude products were further purified by recrystalization with EtOAc/Hexane, which afforded diketo-acids 18a-h in excellent yields (up to 97%). Compounds 18a-h were used for next step without any further purification.
General Procedure for the Synthesis of Functionalized (Z)-3-(2-Oxo-2-Phenylethylidene)-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-one (20a-ab)
To a solution of the compound 18a-h (0.20 mmol; 1eq.) in water (2.0 mL) was added compound 19a-f (0.20 mmol; 1eq.) and the reaction mixture was irradiated under ultrasonic sonicator at 80°C temperature for about 75-90 min (depending upon the substrate employed). The progress of the reaction was checked by TLC using 9:1 Hexane/ethyl acetate as an eluent. After completion of reaction, the reaction mixture was extracted with ethyl acetate (3 × 50 ml); then with distilled water (2 × 10 mL) followed by brine solution (2 × 20 mL). The organic layers were combined and dried over anhydrous Na2SO4 and the organic solvent was removed under reduced pressure to give the crude product. The crude products were purified either by recrystalization using Hexane/EtOAc (v/v = 90:10) or by flash column chromatography method over silica gel using 7.5:2.5 to 9:1 Hexane/ethyl acetate as an eluent which afforded the pure desired (Z)-3-(2-oxo-2-phenylethylidene)-3,4-dihydro-2H-benzo[b][1,4]-oxazin-2-one 20a-ab having good yields (80–98%).
Characterization Data of 2-oxo-benzo[1,4]oxazin-2-one (20a-ab)
(Z)-3-(2-oxo-2-phenylethylidene)-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-one (20a)
Yellow solid; yield: 51.97 mg (98%), Rf (EtOAc/Hexane; 20:80) = 0.85; Purification of crude product was done by flash column chromatography method over silica gel using Hexane/ethyl acetate (9:1) as an eluent; m.p. 185–186°C; FT-IR (KBr, νmax/cm−1) 3434, 1754, 1614, 1594, 1270, 1113; 1H NMR (400 MHz, CDCl3) δ 8.00 (d, J = 7.4 Hz, 2H, Ar-H), 7.55–7.46 (m, 3H, Ar-H), 7.21–7.05 (m, 5H, C=CH, Ar-H); 13C NMR (100 MHz, CDCl3) δ 191.6 (C=O), 156.3 (O=C-O), 141.3 (C=CH), 139.1 (Ar-C), 138.3 (Ar-C), 132.8 (NH-C), 128.8 (Ar-C-NH), 127.7 (Ar-C), 126.0 (Ar-C), 124.0 (Ar-C), 123.8 (Ar-C), 117.2 (Ar-C), 116.0 (Ar-C), 94.7 (C=CH); HRMS (ESI) calcd. for C16H11NO3 [M+H]+: 266.0739; found 266.0734.
(Z)-3-[2-(4-Methoxy-phenyl)-2-oxo-ethylidene]-3,4-dihydro-benzo [1, 4] oxazin-2-one (20b)
Yellowish solid; yield: 51.2 mg (88%), Rf (EtOAc/Hexane; 20:80) = 0.80; Purification of crude product was done by flash column chromatography method over silica gel using Hexane/ethyl acetate (8:2) as an eluent; m.p. 200–203°C; FT-IR (KBr, νmax/cm-1) 3435, 1756, 1602, 1112; 1H NMR (400 MHz, CDCl3) δ 7.99 (d, J = 8.8 Hz, 2H, Ar-H), 7.17 (t, J = 7.1 Hz, 2H, Ar-H), 7.09–7.05 (m, 2H, C=CH, Ar-H), 7.02–6.95 (m, 3H, Ar-H), 3.87 (s, 3H, O-CH3); 13C NMR (100 MHz, CDCl3) δ 190.5 (C=O), 163.5 (Ar-C-OCH3), 156.6 (O=C-O), 141.2 (Ar-C-N), 138.6 (Ar-C-O), 131.2 (C=CH), 130.0 (Ar-C), 125.9 (Ar-C), 124.0 (Ar-C), 123.7 (Ar-C), 117.2 (Ar-C), 115.8 (Ar-C), 114.0 (Ar-C), 94.7 (C=CH), 55.6 (O-CH3); HRMS (ESI) calcd. for C17H13NO4 [M+H]+: 296.0845; found 296.0849.
(Z)-6-chloro-3-(2-oxo-2-phenylethylidene)-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-one (20c)
Yellowish solid; yield: 56.93 mg (95%), Rf (EtOAc/Hexane; 20:80) = 0.80; Purification of crude product was done by flash column chromatography method over silica gel using Hexane/ethyl acetate (8.5:1.5) as an eluent; m.p. 185–187°C; FT-IR (KBr, νmax/cm−1) 3434, 1761, 1555, 1622, 1174; 1H NMR (400 MHz, CDCl3) δ 8.00–7.98 (m, 2H, Ar-H), 7.58–7.55 (m, 1H, Ar-H), 7.50-7.47 (m, 2H, Ar-H), 7.13–7.03 (m, 4H, Ar-H, C=CH); 13C NMR (100 MHz, CDCl3) δ 191.8 (C=O), 155.8 (O=C-O), 139.8 (Ar-C-N), 138.4 (Ar-C-O), 138.1 (C=CH), 133.0 (Ar-C), 131.1 (Ar-C-Cl), 128.9 (Ar-C), 127.8 (Ar-C), 124.8 (Ar-C), 123.8 (Ar-C), 118.3 (Ar-C), 115.8 (Ar-C), 95.7 (C=CH); HRMS (ESI) calcd. for C16H10ClNO3 [M+2]+: 301.7085; found 301.7089.
(Z)-6-chloro-3-(2-(4-fluorophenyl)-2-oxoethylidene)-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-one (20d)
Yellowish solid; yield: 59.08 mg (93%); Rf (EtOAc/Hexane; 20:80) = 0.80; Purification of crude product was done by flash column chromatography method over silica gel using Hexane/ethyl acetate (8.5:1.5) as an eluent; m.p. 155–157°C; FT-IR (KBr, νmax/cm−1) 3434,1754,1634,1601,1495, 1226,1160; 1H NMR (400 MHz, CDCl3) δ 8.06-8.02 (m, 2H, Ar-H), 7.20-7.13 (m, 4H, Ar-H), 7.08-7.04 (m, 2H, C=CH, Ar-H);13C NMR (100 MHz, CDCl3) δ 190.4 (C=O), 167.2 (Ar-C-F), 155.8 (O=C-O), 139.8 (Ar-C-N), 138.6 (Ar-C-O), 131.3 (Ar-C-Cl), 130.5 (C=CH), 130.4 (Ar-C), 124.8 (Ar-C), 123.9 (Ar-C), 118.4 (Ar-C), 116.2 (Ar-C), 115.9 (Ar-C), 115.8 (Ar-C), 95.4 (C=CH); HRMS (ESI) calcd. for C16H9ClFNO3 [M+H]+: 318.0255; found 318.0259.
(Z)-6-chloro-3-(2-(4-chlorophenyl)-2-oxoethylidene)-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-one (20e)
Yellowish solid; yield: 63.9 mg (96%); Rf (EtOAc/Hexane; 20:80) = 0.90; Purification of crude product was done by flash column chromatography method over silica gel using Hexane/ethyl acetate (9:1) as an eluent; m.p. 182–185°C; FT-IR (KBr, νmax/cm−1) 3434, 1761, 1631, 1586, 1088; 1H NMR (400 MHz, CDCl3) δ 7.93 (d, J = 8.2 Hz, 2H, Ar-H), 7.45 (d, J = 8.1 Hz, 2H, Ar-H), 7.13–7.00 (m, 4H, C=CH, Ar-H); 13C NMR (100 MHz, CDCl3) δ 190.4 (C=O), 155.7 (O=C-O), 139.8 (Ar-C-Cl), 139.4 (Ar-C-N), 138.7 (Ar-C-O), 136.3 (C=CH), 131.2 (Ar-C), 129.2 (Ar-C), 129.1 (Ar-C), 124.6 (Ar-C), 124.0 (Ar-C), 118.3 (Ar-C), 115.9 (Ar-C), 95.3 (C=CH); HRMS (ESI) calcd. for C16H9Cl2NO3 [M+2]+: 334.9959; found 334.9956.
(Z)-6-chloro-3-(2-(2,4-dichlorophenyl)-2-oxoethylidene)- 3,4-dihydro-2H-benzo[b][1,4]oxazine-2-One (20f)
Yellowish solid; yield: 65.9 mg (89%); Rf (EtOAc/Hexane; 20:80) = 0.85; Purification of crude product was done by flash column chromatography method over silica gel using Hexane/ethyl acetate (9:1) as an eluent; m.p. 135–137°C; FT-IR (KBr, νmax/cm-1) 3432, 3075, 2923, 1626, 1583, 1105; 1H NMR (400 MHz, CDCl3) δ 7.54 (d, J = 8.4 Hz, 1H, Ar-H), 7.47 (d, J = 1.6 Hz, 1-H, Ar-H), 7.34 (dd, J = 1.6 Hz, 8.4 Hz, 1H, Ar-H), 7.17-7.09 (m, 3H, Ar-H), 6.82 (s, 1H, C=CH); 13C NMR (100 MHz, CDCl3) δ 192.1 (C=O), 155.4 (O=C-O), 139.9 (Ar-C-Cl), 138.4 (Ar-C-Cl), 137.7 (Ar-C-N), 137.2 (Ar-C-O), 132.7 (C=CH), 131.3 (Ar-C), 130.8 (Ar-C), 130.7 (Ar-C), 127.6 (Ar-C), 124.4 (Ar-C), 118.4 (Ar-C), 116.1 (Ar-C), 99.3 (C=CH); HRMS (ESI) calcd. for C16H8Cl3NO3 [M+2]+: 368.9570; found 368.9577.
(Z)-3-(2-(4-bromophenyl)-2-oxoethylidene)-6-chloro-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-one (20g)
Yellowish solid; yield: 70.7 mg (93%); Rf (EtOAc/Hexane; 20:80) = 0.80; Purification of crude product was done by flash column chromatography method over silica gel using Hexane/ethyl acetate (9:1) as an eluent; m.p. 175–177°C; FT-IR (KBr, νmax/cm−1) 3436, 2924, 1755, 1632, 1583, 1007; 1H NMR (400 MHz, CDCl3) δ 7.85 (d, J = 7.9 Hz, 2H, Ar-H), 7.62 (d, J = 7.9 Hz, 2H, Ar-H), 7.13 – 7.00 (m, 4H, Ar-H, C=CH); 13C NMR (100 MHz, CDCl3) δ 190.5 (C=O), 155.6 (O=C-O), 139.8 (Ar-C-N), 138.8 (Ar-C-O), 136.8 (C=CH), 132.1 (Ar-C-Cl), 131.2 (Ar-C), 129.3 (Ar-C-Br), 128.1 (Ar-C), 124.6 (Ar-C), 124.0 (Ar-C), 118.3 (Ar-C), 115.9 (Ar-C), 95.2 (C=CH); HRMS (ESI) calcd. for C16H9BrClNO3 [M+2]+: 377.9454; found 377.9458.
(Z)-6-chloro-3-(2-oxo-2-(p-tolyl)ethylidene)-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-one (20h)
Yellowish solid; yield: 56.5 mg (90%); Rf (EtOAc/Hexane; 20:80) = 0.90; Purification of crude product was done by flash column chromatography method over silica gel using Hexane/ethyl acetate (9.5:0.5) as an eluent; m.p. 160–162°C; FT-IR (KBr, νmax/cm-1) 3434, 2925, 1624, 1766, 1494, 1178; 1H NMR (400 MHz, CDCl3) δ 7.94–7.92 (m, 2H, Ar-H), 7.30 (d, J = 8.0 Hz, 2H, Ar-H), 7.14-7.04 (m, 4H, C=CH, Ar-H), 2.44 (s, 3H, Ar-CH3);13C NMR (100 MHz, CDCl3) δ 191.6 (C=O), 156.0 (O=C-O), 144.0 (Ar-C-CH3), 139.8 (Ar-C-N), 138.2 (Ar-C-O), 135.6 (C=CH), 131.2 (Ar-C), 129.7 (Ar-C), 128.0 (Ar-C), 125.0 (Ar-C), 123.7 (Ar-C), 118.3 (Ar-C), 115.8 (Ar-C), 95.9 (C=CH), 21.8 (-CH3); HRMS (ESI) calcd. for C17H12ClNO3 [M+H]+: 314.0506; found 314.0509.
(Z)-6-chloro-3-(2-(4-methoxyphenyl)-2-oxoethylidene)-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-one (20i)
Yellowish solid; yield: 56.6 mg (86%); Rf (EtOAc/Hexane; 20:80) = 0.80; Purification of crude product was done by flash column chromatography method over silica gel using Hexane/ethyl acetate (9:1) as an eluent; m.p. 178-180°C; FT-IR (KBr, νmax/cm−1) 3434, 1764, 1628, 1594, 1018; 1H NMR (400 MHz, CDCl3) δ 7.99-7.97 (m, 2H, Ar-H), 7.10-7.06 (m, 2H, Ar-H), 7.02–6.99 (m, 2H, Ar-H), 6.97-6.94 (m, 2H, Ar-H, C=CH), 3.87 (s, 3H, OCH3); 13C NMR (100 MHz, CDCl3) δ 190.5 (C=O), 163.7 (Ar-C-OCH3), 156.1 (O=C-O), 139.6 (Ar-C-N), 137.8 (Ar-C-O), 131.1 (C=CH), 130.9 (Ar-C), 130.1 (Ar-C), 125.0 (Ar-C), 123.4 (Ar-C), 118.2 (Ar-C), 115.6 (Ar-C), 114.1 (Ar-C), 95.7 (C=CH), 55.6 (-OCH3); HRMS (ESI) calcd. for C17H12ClNO4 [M+2]+: 331.7345; found 331.7349.
(Z)-3-(2-(4-fluorophenyl)-2-oxoethylidene)-6-methyl-3,4-dihydro-2H-benzo[1,4]oxazin-2-one (20j)
Yellowish solid; yield: 53.7 mg (90%); Rf (EtOAc/Hexane; 20:80) = 0.85; Purification of crude product was done by flash column chromatography method over silica gel using Hexane/ethyl acetate (9.5:0.5) as an eluent; m.p. 145–147°C; FT-IR (KBr, νmax/cm−1) 3433, 2930, 1770, 1624, 1596, 1128; 1H NMR (400 MHz, CDCl3) δ 8.02 (dd, J = 5.6, 8.8 Hz, 2H, Ar-H), 7.17–7.07 (m, 3H, Ar-H), 6.98–6.90 (m, 3H, C=CH, Ar-H), 2.36 (s, 3H, CH3); 13C NMR (100 MHz, CDCl3) δ 190.0 (C=O), 166.9 (Ar-C-F), 156.4 (O=C-O), 139.3 (Ar-C-CH3), 136.1 (Ar-C-N), 134.7 (Ar-C-O), 130.3 (C=CH), 130.2 (Ar-C), 124.9 (Ar-C), 123.3 (Ar-C), 116.9 (Ar-C), 116.2 (Ar-C), 115.9 (Ar-C), 115.8 (Ar-C), 94.1 (C=CH), 21.1 (CH3); HRMS (ESI) calcd. for C17H12FNO3 [M+H]+: 298.0801; found 298.0807.
(Z)-3-[2-(2,4-Dichloro-phenyl)-2-oxo-ethylidene]-6-methyl-3,4-dihydro-benzo[1,4]oxazin-2-one (20k)
Yellowish solid; yield: 65.4 mg (94%), Rf (EtOAc/Hexane; 20:80) = 0.80; Purification of crude product was done by recrystalization using Hexane/ethyl acetate; m.p. 142–145°C; FT-IR (KBr, νmax/cm−1) 3436, 2913, 1755, 1618, 1570, 1083; 1H NMR (400 MHz, CDCl3) δ 7.53 (d, J = 8.3 Hz, 1H, Ar-H), 7.45 (d, J = 2.0 Hz, 1H, Ar-H), 7.33–7.30 (m, 1H, Ar-H), 7.10–7.08 (m, 1H, Ar-H), 6.94–6.92 (m, 2H, Ar-H), 6.73 (s, 1H, C=CH), 2.36 (s, 3H, CH3); 13C NMR (100 MHz, CDCl3) δ 191.6 (C=O), 155.9 (O=C-O), 139.5 (Ar-C-CH3), 139.2 (Ar-C-Cl), 137.5 (Ar-C-Cl), 137.2 (Ar-C-N), 136.2 (Ar-C-O), 132.5 (C=CH), 130.7 (Ar-C), 130.6 (Ar-C), 127.4 (Ar-C), 125.4 (Ar-C), 123.0 (Ar-C), 117.0 (Ar-C), 116.4 (Ar-C), 98.0 (C=CH), 21.1 (CH3); HRMS (ESI) calcd. for C17H11Cl2NO3 [M+2]+: 349.0116; found 349.0112.
(Z)-3-[2-(4-Methoxy-phenyl)-2-oxo-ethylidene]-6-methyl-3,4-dihydro-benzo[1,4]oxazin-2-one (20l)
Yellowish solid; yield: 57.7 mg (93%), Rf (EtOAc/Hexane; 20:80) = 0.75; Purification of crude product was done by flash column chromatography method over silica gel using Hexane/ethyl acetate (8:2) as an eluent; m.p. 180–182°C; FT-IR (KBr, νmax/cm−1) 3452, 1755, 1625, 1581; 1H NMR (400 MHz, CDCl3) δ 7.99 (d, J = 8.8 Hz, 2H, Ar-H), 7.06 (d, J = 8.0 Hz, 1H, Ar-H), 7.00 (s, 1H, Ar-H), 6.96 (d, J = 9.4 Hz, 2H, Ar-H), 6.88 – 6.86 (m, 2H, Ar-H, C=CH), 3.88 (s, 3H, OCH3), 2.34 (s, 3H, CH3); 13C NMR (100 MHz, CDCl3) δ 190.4 (C=O), 163.4 (Ar-C-OCH3), 156.8 (O=C-O), 139.3 (Ar-C-CH3), 138.7 (Ar-C-N), 136.0 (Ar-C-O), 131.3 (C=CH), 129.9 (Ar-C), 124.4 (Ar-C), 123.6 (Ar-C), 116.8 (Ar-C), 116.0 (Ar-C), 114.0 (Ar-C), 94.5 (C=CH), 55.6 (OCH3), 21.1 (CH3); HRMS (ESI) calcd. for C18H15NO4 [M+H]+: 310.1001; found 310.1009.
(Z)-8-bromo-6-methyl-3-(2-oxo-2-phenylethylidene)-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-one (20m)
Yellowish solid; Yield: 65.7 mg (92%); Rf (EtOAc/Hexane; 20:80) = 0.80; Purification of crude product was done by flash column chromatography method over silica gel using Hexane/ethyl acetate (8.5:1.5) as an eluent; m.p. 190–192°C; FT-IR (KBr, νmax/cm−1) 3417, 1767, 1626, 1583, 1282, 1177; 1H NMR (400 MHz, CDCl3) δ 8.00 (d, J = 7.2 Hz, 2H, Ar-H), 7.58-7.47 (m, 3H, Ar-H), 7.13 (s, 1H, Ar-H), 7.07 (s, 1H, C=CH), 6.85 (s, 1H, Ar-H), 2.34 (s, 3H, CH3); 13C NMR (100 MHz, CDCl3) δ 191.7 (C=O), 155.7 (O=C-O), 138.6 (Ar-C-N), 138.1 (Ar-C-O), 136.9 (C=CH), 136.6 (Ar-C-CH3), 132.9 (Ar-C), 128.9 (Ar-C), 128.2 (Ar-C), 127.8 (Ar-C), 124.7 (Ar-C), 115.5 (Ar-C), 110.2 (Ar-C-Br), 95.2 (C=CH), 20.9 (CH3); HRMS (ESI) calcd. for C17H12BrNO3 [M+2]+: 359.0001; found 359.0008.
(Z)-8-bromo-3-(2-(4-fluorophenyl)-2-oxoethylidene)-6-methyl-3,4-dihydro-2H-benzo[b][1,4] oxazin-2-one (20n)
Yellowish solid; Yield: 67.6 mg (90 %); Rf (EtOAc/Hexane; 20:80) = 0.80; Purification of crude product was done by recrystalization using EtOAc/Hexane; m.p. 230–232°C; FT-IR (KBr, νmax/cm−1) 3417, 1771, 1631, 1285, 1159; 1H NMR (400 MHz, CDCl3) δ 8.03-7.99 (m, 2H, Ar-H), 7.17-7.13 (m, 3H, Ar-H), 6.99 (s, 1H, Ar-H), 6.84 (brs, 1H, C=CH), 2.34 (s, 3H, CH3); 13C NMR (100 MHz, CDCl3) δ 190.1 (C=O), 167.0 (Ar-C-F), 164.5 (Ar-C-F), 155.6 (O=C-O), 138.7 (Ar-C-N), 136.9 (Ar-C-O), 136.6 (C=CH), 134.5 (Ar-C-CH3), 134.4 (Ar-C), 130.4 (Ar-C), 130.3 (Ar-C), 128.3 (Ar-C), 124.6 (Ar-C-Br), 116.1 (Ar-C), 115.9 (Ar-C), 115.5 (Ar-C), 110.2 (Ar-C), 94.8 (C=CH), 20.9 (CH3); HRMS (ESI) calcd. for C17H11BrFNO3 [M+2]+: 376.9906; found 376.9909.
(Z)-8-bromo-3-(2-(2,4-dichlorophenyl)-2-oxoethylidene)-6-methyl-3,4-dihydro-2H-benzo [b][1,4]oxazin-2-one (20o)
Yellowish solid; Yield: 79.7 mg (94%); Rf (EtOAc/Hexane; 20:80) = 0.85; Purification of crude product was done by recrystalization using Hexane/ethyl acetate; m.p. 224–226°C; FT-IR (KBr, νmax/cm−1) 3417, 1763, 1626, 1561, 1294, 1127; 1H NMR (400 MHz, CDCl3) δ 7.54 (d, J = 8.4 Hz, 1H, Ar-H), 7.47 (s, 1H, Ar-H), 7.33 (d, J = 8.0 Hz, 1H, Ar-H), 7.18 (s, 1H, Ar-H), 6.88 (s, 1H, C=CH), 6.79 (s, 1H, Ar-H), 2.35 (s, 3H, CH3); 13C NMR (100 MHz, CDCl3) δ 191.9 (C=O), 155.2 (O=C-O), 138.7 (Ar-C-Cl), 137.5 (Ar-C-N), 137.3(Ar-C-O), 137.0 (C=CH), 136.8 (Ar-C-CH3), 132.7 (Ar-C-Cl), 130.8 (Ar-C), 130.7 (Ar-C), 128.8 (Ar-C), 127.5 (Ar-C), 124.3 (Ar-C), 115.7 (Ar-C), 110.3 (Ar-C), 98.8 (C=CH), 20.9 (CH3); HRMS (ESI) calcd. for C17H10BrCl2NO3 [M+2]+: 426.9221; found 426.9227.
(Z)-8-bromo-3-(2-(4-bromophenyl)-2-oxoethylidene)-6-methyl-3,4-dihydro-2H-benzo[b] [1,4]oxazin-2-one (20p)
Yellowish solid; Yield: 77.6 mg (89%); Rf (EtOAc/Hexane; 20:80) = 0.90; Purification of crude product was done by flash column chromatography method over silica gel using Hexane/ethyl acetate (9.5:0.5) as an eluent; m.p. 259–260°C; FT-IR (KBr, νmax/cm−1) 3417, 1768, 1629, 1562, 1283, 1138; 1H NMR (400 MHz, CDCl3) δ 7.86 (d, J = 8.8 Hz, 2H, Ar-H), 7.62 (d, J = 8.4 Hz, 2H, Ar-H), 7.16 (s, 1H, Ar-H), 7.00 (s, 1H, Ar-H), 6.86 (s, 1H, C=CH), 2.35 (s, 3H, CH3); 13C NMR (100 MHz, CDCl3) δ 190.4 (C=O), 155.6 (O=C-O), 139.0 (Ar-C-N), 137.0 (Ar-C-O), 136.9 (C=CH), 136.7 (Ar-C-CH3), 132.2 (Ar-C), 129.3 (Ar-C), 128.5 (Ar-C), 128.1 (Ar-C), 124.5 (Ar-C), 115.6 (Ar-C), 110.3 (Ar-C), 94.8 (C=CH), 20.9 (CH3); HRMS (ESI) calcd. for C17H11Br2NO3 [M+2]+: 436.9106; found 436.9100.
(Z)-8-bromo-6-methyl-3-(2-oxo-2-(p-tolyl)ethylidene)-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-one (20q)
Yellowish solid; Yield: 70.7 mg (95%); Rf (EtOAc/Hexane; 20:80) = 0.90; Purification of crude product was done by flash column chromatography method over silica gel using Hexane/ethyl acetate (8.5:1.5) as an eluent; m.p. 219–220°C; FT-IR (KBr, νmax/cm−1) 3417, 1764, 1630, 1602, 1281, 1182; 1H NMR (400 MHz, CDCl3) δ 7.86 (d, J = 8.4 Hz, 2H, Ar-H), 7.26–7.24 (m, 2H, Ar-H), 7.08 (s, 1H, Ar-H), 7.00 (s, 1H, Ar-H), 6.80 (s, 1H, C=CH), 2.39 (s, 3H, CH3), 2.30 (s, 3H, CH3); 13C NMR (100 MHz, CDCl3) δ 191.4 (C=O), 155.8 (O=C-O), 143.9 (Ar-C-CH3), 138.3 (Ar-C-N), 136.8 (Ar-C-O), 136.5 (C=CH), 135.6 (Ar-C-CH3), 129.6 (Ar-C), 128.0 (Ar-C), 127.9 (Ar-C), 124.8 (Ar-C), 115.4 (Ar-C), 110.1 (Ar-C), 95.3 (C=CH), 21.8 (CH3), 20.9 (CH3); HRMS (ESI) calcd. for C18H14BrNO3 [M+2]+: 373.0157; found 373.0152.
(Z)-6-methyl-3-(2-(4-nitrophenyl)-2-oxoethylidene)-3,4-dihydro-2H-benzo[1,4]oxazin-2-one (20r)
Yellowish solid; yield: 57.2 mg (82%), Rf (EtOAc/Hexane; 20:80) = 0.75; Purification of crude product was done by recrystalization using Hexane/ethyl acetate; m.p. 211–213°C; FT-IR (KBr, νmax/cm−1) 3446, 3072, 1758, 1621, 1515, 1183; 1H NMR (400 MHz, CDCl3) δ 8.32 (d, J = 8.4 Hz, 2H, Ar-H), 8.13 (d, J = 8.4 Hz, 2H, Ar-H), 7.12 (d, J = 7.6 Hz, 1H, Ar-H), 7.01–6.96 (m, 3H, Ar-H, C=CH), 2.37 (s, 3H, CH3); 13C NMR (100 MHz, CDCl3) δ 188.8 (C=O), 155.9 (O=C-O), 149.9 (Ar-C-NO2), 143.3 (C=CH), 140.5 (Ar-C-N), 139.7 (Ar-C-O), 136.4 (Ar-C), 128.6 (Ar-C), 125.8 (Ar-C), 124.0 (Ar-C), 123.9 (Ar-C), 117.2 (Ar-C), 116.7 (Ar-C), 94.1 (C=CH), 21.1 (CH3); HRMS (ESI) calcd. for C17H12N2O5 [M+H]+: 325.0746; found 325.0748.
(Z)-3-(2-(4-nitrophenyl)-2-oxoethylidene)-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-one (20s)
Yellowish solid; yield: 52.2 mg (84%); Rf (EtOAc/Hexane; 20:80) = 0.75; Purification of crude product was done by recrystalization using Hexane/ethyl acetate; m.p. 207–209°C; FT-IR (KBr, νmax/cm−1) 3448, 3069, 1758, 1621, 1515; 1453; 1H NMR (400 MHz, CDCl3) δ 8.32 (d, J = 8.8 Hz, 2H, Ar-H), 8.15 (d, J = 7.2 Hz, 2H, Ar-H), 7.26 – 7.17 (m, 4H, Ar-H), 7.04 (s, 1H, C=CH); 13C NMR (100 MHz, CDCl3) δ 188.9 (C=O), 155.8 (O=C-O), 150.1 (Ar-C-NO2), 143.3 (Ar-C-N), 141.7 (C=CH), 140.5 (Ar-C-O), 128.7 (Ar-C), 126.2 (Ar-C), 125.1 (Ar-C), 124.1 (Ar-C), 123.4 (Ar-C), 117.5 (Ar-C), 116.6 (Ar-C), 94.3 (C=CH); HRMS (ESI) calcd. for C16H10N2O5 [M+H]+: 311.0590; found 311.0596.
(Z)-6-nitro-3-(2-oxo-2-phenylethylidene)-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-one (20t)
Yellowish solid; yield: 55.21 mg (89%); Rf (EtOAc/Hexane; 20:80) = 0.75; Purification of crude product was done by flash column chromatography method over silica gel using Hexane/ethyl acetate (7.5:2.5) as an eluent; m.p. 198–200°C; FT-IR (KBr, νmax/cm−1) 3436, 2928, 1762, 1625, 1581, 1142; 1H NMR (400 MHz, CDCl3) δ 8.03-7.96 (m, 4H, Ar-H), 7.61-7.49 (m, 3H, Ar-H), 7.31 (d, J = 8.8 Hz, 1H, Ar-H), 7.15 (s, 1H, C=CH); 13C NMR (100 MHz, CDCl3) δ 192.1 (C=O), 155.1 (O=C-O), 145.2 (Ar-C-NO2), 144.9 (C=CH), 137.7 (Ar-C-N), 137.6 (Ar-C-O), 133.4 (Ar-C), 128.9 (Ar-C), 127.9 (Ar-C), 124.7 (Ar-C), 118.9 (Ar-C), 118.0 (Ar-C), 111.5 (Ar-C), 96.9 (C=CH); HRMS (ESI) calcd. for C16H10N2O5 [M+H]+: 311.0590; found 311.0593.
(Z)-3-(2-(4-fluorophenyl)-2-oxoethylidene)-6-nitro-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-one (20u)
Yellowish solid; yield: 61.71 mg (94%); Rf (EtOAc/Hexane; 20:80) = 0.75; Purification of crude product was done by flash column chromatography method over silica gel using Hexane/ethyl acetate (8:2) as an eluent; m.p. > 250°C; FT-IR (KBr, νmax/cm−1) 3435, 3107, 1759,1622, 1594, 1156; 1H NMR (400 MHz, DMSO-d6) δ 8.73 (s, 1H, Ar-H), 8.11 (d, J = 5.2 Hz, 2H, Ar-H), 7.92 (d, J = 6.4 Hz, 1H, Ar-H), 7.44 – 7.36 (m, 3H, Ar-H), 6.92 (s, 1H, C=CH); 13C NMR (100 MHz) δ 188.7 (C=O), 166.6, (Ar-C-F), 156.0 (O=C-O), 145.9 (Ar-C-NO2), 144.6 (C=CH), 139.5 (Ar-C-N), 135.1 (Ar-C-O), 130.9 (Ar-C), 125.8 (Ar-C), 118.9 (Ar-C), 117.7 (Ar-C), 116.6 (Ar-C), 116.4 (Ar-C), 113.0 (Ar-C), 94.5 (C=CH); HRMS (ESI) calcd. for C16H9FN2O5 [M+H]+: 329.0495; found 329.0490.
(Z)-3-(2-(4-methoxyphenyl)-2-oxoethylidene)-6-nitro-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-one (20v)
Yellowish solid; yield: 58.51 mg (86%); Rf (EtOAc/Hexane; 20:80) = 0.75; Purification of crude product was done by flash column chromatography method over silica gel using Hexane/ethyl acetate (7:3) as an eluent; m.p. 195–197°C; FT-IR (KBr, νmax/cm−1) 3435, 2926, 1599, 1758, 1633, 1594; 1H NMR (400 MHz, CDCl3) δ 8.02–7.93 (m, 4H, Ar-H), 7.29 (d, J = 8.9 Hz, 1H, Ar-H), 7.10 (s, 1H, C=CH), 6.98 (d, J = 8.7 Hz, 2H, Ar-H), 3.89 (s, 3H, OCH3); 13C NMR (100 MHz, CDCl3) δ 190.7 (C=O), 164.0 (Ar-C-OCH3), 155.3 (O=C-O), 145.2 (Ar-C-NO2), 144.9 (Ar-C-N), 137.0 (Ar-C-O), 130.7 (C=CH), 130.3 (Ar-C), 124.9 (Ar-C), 118.6 (Ar-C), 117.8 (Ar-C), 114.2 (Ar-C), 111.2 (Ar-C), 97.0 (C=CH), 55.7 (OCH3); HRMS (ESI) calcd. for C17H12N2O6 [M+H]+: 341.0695; found 341.0692.
(Z)-7-nitro-3-(2-oxo-2-phenylethylidene)-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-one (20w)
Yellowish solid; yield: 55.22 mg (89%); Rf (EtOAc/Hexane; 20:80) = 0.70; Purification of crude product was done by flash column chromatography method over silica gel using Hexane/ethyl acetate (7.5:2.5) as an eluent; m.p. 240–242°C; FT-IR (KBr, νmax/cm-1) 3436, 1763, 1622, 1596, 1268; 1H NMR (400 MHz, CDCl3) δ 8.06 – 8.00 (m, 4H, Ar-H), 7.83–7.81 (m, 1H, Ar-H), 7.62 (t, J = 7.3 Hz, 1H, Ar-H), 7.54 (t, J = 7.5 Hz, 2H, Ar-H), 6.99 (s, 1H, C=CH); 13C NMR (100 MHz, CDCl3) δ 190.7 (C=O), 156.1 (O=C-O), 142.2 (Ar-C-N), 141.1 (Ar-C-O), 139.2 (Ar-C-NO2), 138.3 (C=CH), 133.6 (Ar-C), 131.3 (Ar-C), 129.6 (Ar-C), 128.0 (Ar-C), 121.4 (Ar-C), 117.4 (Ar-C), 112.6 (Ar-C), 96.0 (C=CH); HRMS (ESI) calcd. for C16H10N2O5 [M+H]+: 311.0590; found 311.0595.
(Z)-3-(2-(4-fluorophenyl)-2-oxoethylidene)-7-nitro-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-one (20x)
Yellowish solid; yield: 52.7 mg (80%); Rf (EtOAc/Hexane; 20:80) = 0.70; Purification of crude product was done by recrystalization using Hexane/ethyl acetate; m.p. 235–237°C; FT-IR (KBr, νmax/cm-1) 3411, 3090, 1773, 1626, 1516, 1473; 1H NMR (400 MHz, DMSO-d6) δ 8.18 - 8.08 (m, 4H, Ar-H), 7.88 – 7.86 (m, 1H, Ar-H), 7.42–7.38 (m, 2H, Ar-H), 7.02 (s, 1H, C=CH); 13C NMR (100 MHz, DMSO-d6) 188.7 (C=O), 163.7 (Ar-C-F), 155.5 (O=C-O), 141.8 (Ar-C-N), 140.6 (Ar-C-O), 138.7 (Ar-C-NO2), 134.4 (C=CH), 130.7 (Ar-C), 130.6 (Ar-C), 130.5 (Ar-C), 120.9 (Ar-C), 116.9 (Ar-C), 116.2 (Ar-C), 115.9 (Ar-C), 112.0 (Ar-C), 95.3 (C=CH); HRMS (ESI) calcd. for C16H9FN2O5 [M+H]+: 329.0495; found 329.0499.
(Z)-3-(2-(4-chlorophenyl)-2-oxoethylidene)-7-nitro-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-one (20y)
Yellowish solid; yield: 59.7 mg (87%); Rf (EtOAc/Hexane; 20:80) = 0.70; Purification of crude product was done by flash column chromatography method over silica gel using Hexane/ethyl acetate (7.5:2.5) as an eluent; m.p. 205–207°C; FT-IR (KBr, νmax/cm-1) 3432, 2925, 2860, 1633, 1525, 1776, 1075; 1H NMR (400 MHz, DMSO-d6) δ 8.08 (d, J = 8.4 Hz, 4H, Ar-H), 7.89-7.87 (m, 1H, Ar-H), 7.63 (d, J = 8.4 Hz, 2H, Ar-H), 7.01 (s, 1H, C=CH); 13C NMR (100 MHz, DMSO-d6) δ 188.9 (C=O), 155.4 (O=C-O), 141.9 (Ar-C-N), 140.7 (Ar-C-Cl), 138.9 (Ar-C-O), 136.5 (Ar-C-NO2), 130.7 (C=CH), 129.8 (Ar-C), 129.5 (Ar-C), 129.2 (Ar-C), 120.9 (Ar-C), 117.0 (Ar-C), 112.1 (Ar-C), 95.2 (C=CH); HRMS (ESI) calcd. for C16H9ClN2O5 [M+H]+: 345.0200; found 345.0207.
(Z)-3-(2-(2,4-dichlorophenyl)-2-oxoethylidene)-7-nitro-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-one (20z)
Yellowish solid; yield: 64.6 mg (85%); Rf (EtOAc/Hexane; 20:80) = 0.70; Purification of crude product was done by recrystalization using Hexane/ethyl acetate; m.p. 208–210°C; FT-IR (KBr, νmax/cm−1) 3433, 3088, 1770, 1620, 1522, 1470, 1072; 1H NMR (400 MHz, DMSO-d6) δ 12.39 (s, 1H, NH), 8.09–8.08 (m, 2H, Ar-H), 7.95–7.93 (s, 1H, Ar-H), 7.78–7.58 (m, 3H, Ar-H), 6.62 (s, 1H, C=CH); 13C NMR (100 MHz, DMSO-d6) δ 190.3 (C=O), 155.3 (O=C-O), 142.2 (Ar-C-N), 140.8 (Ar-C-Cl), 138.5 (Ar-C-O), 137.7 (Ar-C-NO2), 136.2 (C=CH), 131.2 (Ar-C-Cl), 131.0 (Ar-C), 130.5 (Ar-C), 130.1 (Ar-C), 127.9 (Ar-C), 120.8 (Ar-C), 117.3 (Ar-C), 112.1 (Ar-C), 98.8 (C=CH); HRMS (ESI) calcd. for C16H8Cl2N2O5 [M+H]+: 378.9810; found 378.9818.
(Z)-3-(2-(4-bromophenyl)-2-oxoethylidene)-7-nitro-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-one(20aa)
Yellowish solid; yield: 67.7 mg (87%); Rf (EtOAc/Hexane; 20:80) = 0.70; Purification of crude product was done by flash column chromatography method over silica gel using Hexane/ethyl acetate (7.5:2.5) as an eluent; m.p. 230–232°C; FT-IR (KBr, νmax/cm−1) 3435, 3093, 1769, 1619, 1521; 1H NMR (400 MHz, DMSO-d6) δ 8.09-7.96 (m, 4H, Ar-H), 7.83-7.44 (m, 3H, Ar-H), 7.01(d, J = 4.8 Hz, 1H, C=CH); 13C NMR (100 MHz, DMSO-d6) δ 188.9 (C=O), 154.7 (O=C-O), 141.8 (Ar-C-N), 140.1 (Ar-C-O), 137.9 (C=CH), 136.6 (Ar-C-NO2), 131.5 (Ar-C), 130.0 (Ar-C), 129.1 (Ar-C-Br), 126.6 (Ar-C), 120.7 (Ar-C), 116.5 (Ar-C), 111.4 (Ar-C), 95.7 (C=CH); HRMS (ESI) calcd. for C16H9BrN2O5 [M+2]+: 389.9695; found 389.9691.
(Z)-3-(2-(4-methoxyphenyl)-2-oxoethylidene)-7-nitro-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-one (20ab)
Yellowish solid; yield: 55.4 mg (81%); Rf (EtOAc/Hexane; 20:80) = 0.70; Purification of crude product was done by flash column chromatography method over silica gel using Hexane/ethyl acetate (7:3) as an eluent; m.p. 218–220°C; FT-IR (KBr, νmax/cm−1) 3437, 2927, 2854, 1632, 1517; 1H NMR (400 MHz, DMSO-d6) δ 8.07-8.02 (m, 4H, Ar-H), 7.73 (d, J = 10.8 Hz, 1H, Ar-H), 7.09 (d, J = 8.8 Hz, 2H, Ar-H), 7.02 (s, 1H, C=CH), 3.89 (s, 3H, OCH3); 13C NMR (100 MHz, DMSO-d6) δ 189.1 (C=O), 163.4 (Ar-C-OCH3), 155.8 (O=C-O), 141.7 (Ar-C-N), 140.6 (Ar-C-O), 138.1 (C=CH), 131.1 (Ar-C-NO2), 130.7 (Ar-C), 130.1 (Ar-C), 121.2 (Ar-C), 116.8 (Ar-C), 114.5 (Ar-C), 112.2 (Ar-C), 95.9 (C=CH), 55.8 (OCH3); HRMS (ESI) calcd. for C17H12N2O6 [M+H]+: 341.0695; found 341.0699.
Pharmacological Assay Descriptions
DPPH Radical Scavenging Antioxidant Assay
In DPPH radical scavenging method the plant extract (0.75 mL) at different concentrations ranging from 10 to 100 μg mL−1 was mixed with 1.5 mL of a DPPH methanolic solution (20 mg L−1). Pure methanol was taken as control and ascorbic acid (vitamin C), vitamins A and E were used as a reference compounds. The absorbance was measured at 517 nm after 20 min of reaction. The % of DPPH decolouration of the sample was calculated according to the formula (Sharma and Bhat, 2009).
The decolouration was plotted against the sample extract concentration and a logarithmic regression curve was established in order to calculate the IC50. The results are expressed as antiradical efficiency (AE), which is 1000-fold inverse of the IC50 value AE=1000/ IC50.
Ferric Reducing Antioxidant Power (FRAP) Assay
The FRAP reagent was prepared by the addition of freshly prepared 20.0 mM FeCl3.6H2O solution, 10.0 mM of ferric-tripyridyltriazine (TPTZ) solution and 300 mM sodium acetate buffer (pH 3.6) in a ratio of 1:1:10 (v/v/v). After that, Sample (our synthesized 2-oxo-2-phenylethylidenes-linked 2-oxo-benzo[1,4]oxazines 20a-ab) was added to 3 ml of freshly prepared FRAP reagent and this reaction mixture was incubated at 37°C temperature for 30 min. and the absorbance was measured at 593 nm. It is also noted that, a freshly prepared solution of FeSO4 was used for calibration of standard curve. The FRAP antioxidant capability were evaluated in terms of C0.5FRAP (the antioxidant capability of samples related to their concentration, which is equivalent to that of FeSO4 at 0.5 mmol/L) (Benzie and Strain, 1996).
Cell Toxicity Assay
Cell toxicity of active C-3 tethered 2-oxo-benzo[1,4]oxazine analogs were accessed using 3T3 fibroblast cell lines in MTT assay via the reported protocol of Danihelová et al. (2013) [For details, see supporting information].
In Silico Molecular Docking Studies
Molecular modeling studies of C-3 tethered 2-oxo-benzo [1, 4] oxazine derivatives 20a-ab were carried out using molecular modeling software Sybyl-X 2.0, (Tripos International, St. Louis, Missouri, 63144, USA). Drawing of structures and simple geometry optimization were performed with Chem Bio-Office suite Ultra v12.0 (2012) (Cambridge Soft Corp., UK). Docking of all compounds was carried out on the human antioxidant enzyme in complex (PDB ID: 3MNG) (Hall et al., 2010b; Bayoumi et al., 2012; Yapati et al., 2016). The Surflexdoc module in Sybyl was used to construct a 3D model of the structures.
To find the possible bioactive conformations of C-3 tethered 2-oxo-benzo[1,4]oxazine derivatives, molecular modeling studies were performed using the Sybyl X 2.0 interfaced for the synthesized compounds, which exhibited promising and lower antioxidant activity in vitro to find the preferred binding conformations in the receptor. The starting coordinates of the human antioxidant enzyme in complex with the competitive inhibitor DTT (PDB: 3MNG) were taken from the Protein Data Bank (http://www.rcsb.org/pdb). Program automatically docks ligand into binding pocket of a target protein by using protomol-based algorithm and empirically produced scoring function. The protomol is very important and necessary factor for docking algorithm and works as a computational representation of proposed ligand that interacts into binding site. Surflex-Dock's scoring function have several factors that play an important role in the ligand-receptor interaction, in terms of hydrophobic, polar, repulsive, entropic and solvation, and it is a worldwide well-established and recognized method. The most standard docking protocols have ligand flexibility into the docking process, while counts the protein as a rigid structure. Present molecular docking study involves the several steps viz., import of protein structure into Surflex and addition of hydrogen atoms; generation of protomol using a ligand-based strategy. During second step, two parameters first called protomol_bloat, which determines how far the site should extend from a potential ligand; and another called protomol_threshold, which determines deepness of the atomic probes, used to define the protomol penetration into the protein) were specified to form the appropriate binding pocket. Therefore, protomol_bloat and protomol_threshold was set to 0 and 0.50, respectively. In reasonable binding pocket, all the compounds were docked into the binding pocket and 20 possible active docking conformations with different scores were obtained for each compound. During the docking process, all of the other parameters were assigned their default values.
Results and Discussion
Chemistry
The synthetic scheme for the synthesis of desired C-3 tethered 2-oxo-benzo[1,4]oxazine analogs 20a-20ab using our reported procedure (Jaiswal et al., 2017) is depicted in Schemes 1, 2.
Scheme 1. Synthesis of starting substrate functionalized diketo-acid (18a-h).
Scheme 2. Ultrasound-assisted green synthesis of C-3 tethered 2-oxo-benzo [1,4]oxazine analogs (20a-20ab).
The base-mediated reaction of acetophenone 16a-h with dimethyl oxalate in toluene for 6h furnished the diketo-ester 17a-h in 70-80% yields. Conversion of these diketoesters 17a-h to 2, 4-dioxo-4-phenylbutanoic acid 18a-h were achieved by hydrolysis with LiOH.H2O in MeOH:THF:H2O (4:3:1) solvent. The reaction of nitro/alkyl/halide-substituted 2, 4-dioxo-4-phenylbutanoic acid 18a-h with nitro/alkyl/halide-substituted 2-aminophenol 19a-f in water furnished C-3 tethered 2-oxo-benzo[1,4]oxazines 20a-20ab in 74-98% yields after purification either by flash column chromatography or by recrystallization method (Scheme 2, Figure 3; see Supplementary Figures 1–28 for details). All the synthesized compounds were well characterized by 1H-NMR and 13C-NMR spectroscopy, FTIR and HRMS analysis.
Figure 3. Structures of all synthesized C-3 tethered 2-oxo-benzo [1, 4]oxazines (20a-20ab).
Biological Evaluation
DPPH Radical Scavenging Antioxidant Activity and SAR Studies
All the synthesized C-3 tethered 2-oxo-benzo[1,4]oxazine analogs 20a-20ab were evaluated for in vitro antioxidant activities using DPPH radical scavenging assay compared with standard reference ascorbic acid (Table 1). The choice of the reference compounds is based on hydrophilic nature of ascorbic acid and the maximum inhibition of the DPPH radical in IC50 value (μg/mL) by all the compounds 20a-20ab. The DPPH radical scavenging assay is generally utilized as a quick and reliable parameter to investigate the antioxidant activities of diverse heterocycles (Baydar et al., 2007). DPPH is a stable free radical, that can easily accept a hydrogen radical or an electron to become a stable molecule (Blois, 1958). In the methanolic medium, DPPH has odd electron configuration having a strong absorption band at 515 nm, whereas this absorption decreases slightly in the presence of free radical scavengers, and it results color change to yellow from deep purple (Eklund et al., 2005; Sharma and Bhat, 2009). The radical trapping ability strongly depends on the structural availability of the radical trapping site. The steric hindrance as well as electron density plays a dynamic role in the antioxidant activity since they may prevent the test molecule from reaching the radical site of DPPH and thus results in low activity (Faria et al., 2006).
Table 1. Antioxidant activity of synthesized compounds 20a-ab by DPPH radical scavenging assay and FRAP assay.
Kareem et al. proposed two mechanisms involved in DPPH assay; first one is the hydrogen atom transfer (HAT) mechanism and the second one is the single electron transfer (SET) mechanism (Kareem et al., 2015). Similar to their interpretation, it can be speculated that, for DPPH assay, a dominant HAT mechanism is assumed and the favored hydrogen abstraction sites are enamine –NH group, preferably with conjugation to the side chain of phenacyl group (-COPh), as the latter could stabilize by the resulting radical from additional resonance structures.
The generic scaffold of the newly synthesized C-3 tethered 2-oxo-benzo[1,4]oxazines, as illustrated in Figure 4, consists of a two fused cyclic ring A and B linked with ring C via α, β-unsaturated ketone having electron-withdrawing group (EWG) and/or electron-donating group (EDG) either at ring A or at C. The active group -CO-C=C-NH- enables resonance between the ring B and C, leading to multiple resonance structure, which may be further initiated by the attached substituents of ring A and C and in situ enhances the radical scavenging activity through the removal of hydrogen atom from NH of ring B via HAT mechanism. It has been found that electron withdrawing substituent NO2 at ring A or C increase the antioxidant activity which may be due to resonance based stabilizing effects. Therefore, based on the structures and their antioxidant activities, it was found that the compounds have either no substitution at ring A and C or have EWG/EDG at ring A and C plays a very important role in deciding their DPPH radical scavenging activities. Hence, based on the substituent's (either EWG or EDG) at ring A and C of 2-oxo-benzo[1,4]oxazines 20a-20ab, and their antioxidant activities, their structure-activity relationship can be explained by grouping all compounds into two groups:
(i) No substitution or EDG at ring A or ring C: In the first group of compounds having no substitution at ring A and C i.e., the model compound 20a, exhibited promising antioxidant activity (IC50 = 10.20 ± 0.08 μg/mL) in comparison with standard reference Ascorbic acid (IC50 = 4.57 μg/mL) [entry 1]. Then, by putting EDG (OMe group) at ring C, as in compound 20b, further increases activity (IC50 = 6.89 ± 0.07 μg/mL) [entry 2]. Reversing the order i.e., halogen substitution at ring A and no substitution at ring C do not cause any further increase in antioxidant activity as shown by compound 20c (entry 3). Furthermore, when we incorporated halogen substituents (Cl, F, Br, 2,4-dichloro) or CH3 substituent either at A or C as in the case of compounds 20c-l; a decrease in the antioxidant activity was observed due to high electron density in compounds 20d-g, 20j and 20k (entry 4-12). Furthermore, It was observed that two EDG at ring A (20m-q; entry 13-17) exhibited moderate antioxidant activity having IC50 value in the range of 18.86 ± 0.72 to 44.32 ± 0.45 μg/mL. In this series (20m-q; entry 13-17), ring C having Fluorine substituent i.e. compound 20n exhibited good antioxidant activity (IC50 = 16.86 ± 0.72 μg/mL) in comparison with other compounds (20m and 20o-q).
To our surprise; when we incorporated EWG group i.e., NO2 group at ring C and EDG group i.e., CH3 group at ring A (compound 20r); the antioxidant activity was regained and shows IC50 value of 12.23 ± 0.05 μg/mL nearly equivalent to 20a (entry 18).
It is to be noted that EDG at ring A decreases antioxidant activity as shown in entries 3-17; so, we synthesized compound 20s (having no any substitution at ring A and EWG i.e., NO2 group at ring C), which, contrary to our expectations, displayed further decrease in antioxidant activity (IC50 = 21.27 ± 0.28 μg/mL) (entry 19).
(ii) EWG (-NO2 Group) at ring A: Since 20r having EWG (NO2) at ring C showed promising antioxidant activity; inspired by this observation, we prepared 20t-v having NO2 group at C-4 position of ring A. 2-oxo-benzo[1,4]oxazine 20t having no substitution at ring C, showed excellent antioxidant activity having IC50 value of 4.74 ± 0.08 μg/mL (entry 20). Since 20b having OMe substituent at ring C, was also found to show excellent antioxidant activity; thus, we synthesized 20u and 20v having Fluoro as well as OMe substituent, respectively at ring C. Unfortunately, antioxidant activity diminishes (entry 21 and 22). In addition, we also prepared 2-oxo-benzo[1,4]oxazines 20w-20ab having EWG group (NO2) at C-5 position of ring A further to investigate SAR study. Compound 20w having no substitution at ring C showed promising antioxidant activity having IC50 value of 12.53 ± 0.09 μg/mL (entry 23). On incorporating Fluoro group at ring C; activity of 20x increases (IC50 = 10.18 ± 0.10 μg/mL, entry 24). Furthermore, when we incorporated halogen substituents (Cl, Br, 2,4-dichloro and OMe) at ring C as in the case of compounds 20y-20ab; a decrease in the antioxidant activity was observed (entry 19-23).
Overall, we can interpret that no substitution or EWG at ring A or ring C enhances antioxidant activity of all the synthesized 2-oxo-benzo[1,4]oxazines 20a-20ab. Whereas EDG either at ring A or C diminishes antioxidant activity. Our SAR results depict that 20b and 20t, the best compounds of the series, showed antioxidant activity comparable to standard reference Ascorbic acid.
Figure 4. SAR analysis of synthesized 2-oxo-benzo[1,4]oxazines.
Ferric Reducing Antioxidant Power (FRAP) Activity and SAR Studies
The FRAP assay was deliberated using the method as illustrated by Benzie and Strain (Benzie and Strain, 1996). It reveals that the reducing potential of an antioxidant molecule, which reacts with a complex of ferric tripyridyltriazine [Fe3+−TPTZ] and develops a colored ferrous tripyridyltriazine [Fe2+-TPTZ]. The reducing nature of an antioxidant depends on their property to donate a hydrogen atom for the breaking of the free radical chain, which is responsible for oxidative stress etc.
All the synthesized C-3 tethered 2-oxo-benzo[1,4]oxazine analogs 20a-20ab were assessed for FRAP assay taking BHT as standard reference; as depicted in Table 1. In this study, the trend with respect to ferric ion reducing activities of all the screened compounds i.e., 20a-20ab showed that eight compounds (20c, 20j, 20m, 20n, 20r, 20u, 20z, and 20aa) were found more potent than BHT (C0.5FRAP = 546.0 ± 13.6 μM).
In summary, all the compounds (20a-20ab) displayed good to moderate activity in comparison with BHT in the range of C0.5FRAP = 328.6 ± 25.8 μM to 916.8 ± 21.4 μM in in-vitro antioxidant FRAP assay except compounds 20e, 20f, 20l, 20q, 20v, and 20ab which showed C0.5FRAP greater than 1000 μM. Compounds having EWG i.e. NO2 substituent at ring C (20r and 20s) showed different potency than standard reference BHT. While 20r having CH3 at C-4 position of ring A displayed potent activity than BHT; 20s was found to be less active. Anomaly was observed in the case of compounds having no substitution at ring C. While 20c and 20m showed greater potency; compounds 20a, 20t and 20w were found less active than BHT.
Cell Toxicity Study
Out of 28 compounds, three most active compounds i.e., 20b, 20t, and 20x were then selected for their cytotoxic studies. As depicted in Figure 5, compounds 20b, 20t, and 20x were accessed for their cytotoxic study using 3T3 fibroblast cell lines in MTT assay (Danihelová et al., 2013). The result showed that these compounds were non-toxic in nature (>65% cell viability) even at 250 μg/mL concentration and therefore, displays permissible values of cell viability.
Figure 5. Percentage cell viability test.
In Silico Molecular Docking Simulation Studies
Finally, the biological results were validated via in silico molecular docking studies of two most active compounds (20b and 20t). Since 20b has OMe group at ring C and 20t has NO2 group at ring A; it is worthwhile to compare the docking studies of active compounds with molecules having no substitution either at ring A or C. Therefore, we have also selected compound 20a for our in silico molecular docking simulation studies. For that purpose, Peroxiredoxins (Prdxs), a family of small human antioxidant enzyme, was selected as our target protein. Peroxiredoxins contain essential cysteine residues as catalyst and thioredoxin as an electron donor, which help in scavenging peroxide and are involved in the metabolic cellular response to ROS (Neumann et al., 2003; Monteiro et al., 2007).
The binding affinities and interactions of C-3 tethered 2-oxo-benzo [1, 4] oxazine derivatives with the human antioxidant enzyme were investigated through molecular docking simulations. Binding affinities were predicted by the Sybyl docking total score upon docking with the Surflex-Dock program (Sybyl X 2.0).Compounds were docked into the active site of the known the human antioxidant enzyme target peroxiredoxins (Prxs) DTT complex (PDB ID: 3MNG) were taken from the Protein Data Bank (http://www.rcsb.org/pdb) (Hall et al., 2010b; Bayoumi et al., 2012; Yadav et al., 2014a,b; Yapati et al., 2016).
Docking studies were carried out to evaluate the binding affinity and interactions with their target proteins. Hydrogen bonds (H-bonds, with a donor-receptor distance of 3Å) between the ligand and amino acids in the binding site of the protein were used for the ranking of compounds. The mode of interaction of the co-crystallized ligand dithiothreitol (DTT) within the crystal structure of enzyme in complex was used as a reference binding model. The root mean-square deviation (RMSD) of each docking pose was compared to the co-crystallized ligand and used for ranking and for RMSD calculation. The co-crystallized DTT molecule was re-docked onto the same binding site and the most probable binding mode was selected as that with the highest docking total score of 4.8921. An RMSD value 0.6772Å between the predicted and crystal binding mode indicates the high reliability of Surflex-Dock for this protein target.
On the other hand, docking results for 20a, 20b, and 20t against the antioxidant target protein Prxs showed a high binding affinity docking score indicated by a total score of 3.8470 (Figure 6A), 3.6567 (Figure 6B) and 4.2709 (Figure 6C) forms a H-bond (NH2…O) of length 1.8Å to the backbone of hydrophobic aliphatic residue that is, Glycine-46. In the docking pose of the 20a, 20b, and 120t and Prxs complex, the chemical nature of binding site residues within a radius of 3Å with diverse properties was aromatic (hydrophobic), for example, Phe-120, (Phenylalanine); hydrophobic, for example, Leu-116, Ile-119, Leu-149, Leu-112(Leucine), Gly-46, Gly-148(Glycine); (polar, hydrophobic, positive charged) residues, for example, Arg-127 (Arginine); nucleophilic (polar, hydrophobic), for example, Thr-147 and Thr-44 (Threonine), nucleophilic (polar uncharged), for example Cys-47 (Cysteine); and hydrophobic (polar, uncharged) residues, for example, Pro-40 and Pro-45 (Proline) as a result, the bound compound showed a strong hydrophobic interaction with Prxs, thus leading to more stability and activity in this compound.
Figure 6. Binding interactions of compound 20a, 20b, 20t and reference drug Ascorbic acid upon docking onto human antioxidant enzyme target peroxiredoxins (Prxs) (PDB ID: 3MNG). The formation of a H-bond of length 1.8Å to residue Gly-46 in the binding site was predicted in the case of 20a, 20b, and 20t along with the formation of four H-bond of length 2.2, 1.8 and 2.1 Å to residue Thr-147, Gly-46 and Thr-44 in the binding site was predicted in the case of reference drug Ascorbic acid. (A) A top docking energy (total score) of 3.8470 was predicted for 20a; (B) A top docking energy (total score) of 3.6567 was predicted for 20b. (C) A top docking energy (total score) of 4.2709 was predicted for 20t. (D) A top docking energy (total score) of 3.4829 was predicted for Ascorbic acid.
The docking results for the ascorbic acid (standard compound) with the antioxidant target protein Prxs showed a low binding affinity docking score, indicated by a low total score of 3.4829 with three H-bond (hydrogen bond) formation of length 2.2, 1.8 and 2.1Å to the Thr-147, Gly-46 and Thr44 (Figure 6D). The ascorbic acid-Prxc-docked complex also showed a similar type of binding site residues within a radius of 3Å of bound ligand such as Thr-147, Leu-116, Pro-40, Phe-120, Leu-112, Thr-44, Gly-46, Pro-45, Cys-47, Arg-127, Leu-149 shown in Figure 6D. Thus, the docking procedure of Surflex-dock software (Sybyl-X 1.3) in reproducing the experimental binding affinity seems reliable, and therefore predicted as true positive.
Thus, it can be inferred based on docking simulation studies that the most active compounds i.e., 20b and 20t having IC50 value of 6.89 ± 0.07 μg/mL and 4.74 ± 0.08 μg/mL, showed the binding affinity docking score of 3.6567 and 4.2709, respectively (Figures 6B,C), which were found to be comparable to the binding affinity docking score of standard reference ascorbic acid (Figure 6D). While comparing the binding energy docking score of 20a (unsubstituted both at ring A and C) i.e., 3.8470 (Figure 6A) with ascorbic acid and the two most active compounds; the results were also found to be comparable. Thus, the in silico docking results of 20b and 20t successfully validated the in vitro experimental studies.
Conclusion
In summary, we disclose C-3 tethered 2-oxo-benzo [1, 4]oxazine analogs 20a-20ab as a of potent antioxidant agents. Compound 20b and 20t, the most active compounds of the series, showed promising antioxidant activity having IC50 value of 6.89 ± 0.07 μg/mL and 4.74 ± 0.08 μg/mL, respectively, in DPPH radical scavenging assay in comparison with ascorbic acid (IC50 = 4.57 μg/mL). Whereas in FRAP assay, eight compounds (20c, 20j, 20m, 20n, 20r, 20u, 20z, and 20aa) were found more potent than BHT (C0.5FRAP = 546.0 ± 13.6 μM). The active compounds were also found non-toxic in 3T3 fibroblast cell lines in MTT assay. Our in silico molecular docking results reveal that 20b and 20t showed excellent docking total scores against human antioxidant enzyme target as compared to ascorbic acid. Thus, the in silico docking simulation studies effectively validated the in vitro experimental results.
Author Contributions
SC was responsible for the study of concept and design of the project. VS and PKJ were responsible for the performing synthetic reactions, acquisition and analysis of data. MS, MM, and AKS were responsible for the pharmacological in vitro activity evaluation of synthesized compounds. DKY and Saloni performed docking studies. SM and MHK provided molecular modeling facility. SC and PKJ drafted the manuscript. All authors read and approved the final manuscript.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
SC acknowledges SERB, New Delhi for fast track scheme for young scientist (CS-037/2013); DST, New Delhi for DST-RFBR Indo-Russian Joint Research Project (INT/RUS/RFBR/P-169) and CSIR, New Delhi for CSIR-EMR Grant [02 (0189)/14/EMR-II]. PKJ and VS thanks CSIR, New Delhi and MNIT, Jaipur for providing financial assistance in the form of RA fellowship and institute fellowship, respectively. DKY acknowledges SERB, New Delhi for financial support through the Young Scientist Project SB/YS/LS-130/2014 at the All India Institute of Medical Sciences (AIIMS), Jodhpur, India. DKY acknowledges the National Research Foundation of Korea (NRF), which is funded by the Ministry of Education, Science, and Technology (No: 2017R1C1B2003380) at the Gachon University, Incheon city, Korea. Materials Research Centre, MNIT, Jaipur is gratefully acknowledged for providing analytical facilities.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fchem.2018.00056/full#supplementary-material
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Keywords: 2-oxo-benzo[1, 4]oxazines, antioxidant, DPPH, FRAP, ascorbic acid, BHT
Citation: Sharma V, Jaiswal PK, Saran M, Yadav DK, Saloni, Mathur M, Swami AK, Misra S, Kim M and Chaudhary S (2018) Discovery of C-3 Tethered 2-oxo-benzo[1,4]oxazines as Potent Antioxidants: Bio-Inspired Based Design, Synthesis, Biological Evaluation, Cytotoxic, and in Silico Molecular Docking Studies. Front. Chem. 6:56. doi: 10.3389/fchem.2018.00056
Received: 25 November 2017; Accepted: 23 February 2018;
Published: 23 March 2018.
Edited by:
Rajeev K. Singla, Netaji Subhas Institute of Technology, IndiaReviewed by:
Abdul Sadiq, University of Malakand, PakistanLhassane Ismaili, Université Bourgogne Franche-Comté, France
Rohit Gundamaraju, University of Tasmania, Australia
Copyright © 2018 Sharma, Jaiswal, Saran, Yadav, Saloni, Mathur, Swami, Misra, Kim and Chaudhary. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Dharmendra Kumar Yadav, dharmendra30oct@gmail.com
Sandeep Chaudhary, schaudhary.chy@mnit.ac.in
†These authors have contributed equally to this work.