Abstract
A new series of ( ±)-(3-(3,5-dimethyl-1H-pyrazol-1-yl)-6-phenyl-6,7-dihydro-5H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)(phenyl)methanones were efficiently synthesized starting from 4-amino-5-hydrazinyl-4H-1,2,4-triazole-3-thiol 1, acetyl acetone 2, various aromatic and heterocyclic aldehydes 3 and phenacyl bromides 4. All the newly synthesized compounds were tested for their antiviral and antitumoral activity. It was shown that subtle structural variations on the phenyl moiety allowed to tune biological properties toward antiviral or antitumoral activity. Mode-of-action studies revealed that the antitumoral activity was due to inhibition of tubulin polymerization.
Graphic abstract
Supplementary Information
The online version contains supplementary material available at 10.1007/s11030-021-10258-8.
Keywords: Triazole, Pyrazole, Antiviral, Antitumoral, Dihydrothiadiazine, Multi-component reaction
Introduction
Heterocyclic structures are well-known components of various biologically active compounds. Nitrogen-containing hetero aromatics [1–7], such as triazole and pyrazole are well known to impart biological activity. Examples of marketed drugs based on a 1,2,4-triazole scaffold include voriconazole (an antifungal drug), forasartan (used for the treatment of hypertension), sitagliptin (an antidiabetic drug) and letrozole (a non-steroidal aromatase inhibitor for the treatment of breast cancer) (Fig. 1) [8]. In addition, a wide range of 1,2,4-triazole derivatives have been synthesized and tested in a wide variety of biological assays, leading to the discovery of anti-bacterial [9, 10], antiviral [11, 12], antifungal [13, 14], anti-inflammatory [15, 16], anti-proliferative [17, 18], anti-convulsant [19], anti-oxidant [20] and anti-Parkinson [21] triazole analogues. Pyrazole ring is another example of a hetero aromatic scaffold, exhibiting a wide range of biological properties. Examples of drugs based on a pyrazole scaffold that received marketing include celecoxib and deracoxib (both cyclo-oxygenase-2 inhibitors), surinabant (a cannabinoid receptor type 1 antagonist) and crizotinib (an ALK inhibitor). However, a plethora of other activities, such as anti-HIV [22, 23], anti-malarial [24], anti-oxidant [25], anti-inflammatory [26], anti-bacterial [27, 28], anti-tumor [29], anti-pyretic [30], anti-analgesic [31], anti-cancer [32] and anti-leishmanial [33] activities have been associated with the pyrazole scaffold.
Fig. 1.
Marketed drugs based on a 1,2,4-triazole and pyrazole scaffold
Although sulfur-containing heterocyclic compounds were found to have extensive biological applications, 1,3,4-thiadiazines are explored to a much lesser extent in medicinal chemistry, when compared to 1,2,4-triazole and pyrazole motifs. Thiadiazines are themselves showing good biological activities [34–39].
Multi-component reactions (MCRs), also known as multi-component assembly processes (MCAPs), are attractive synthetic methodologies in medicinal chemistry. The synthetic procedures in MCRs use mild reaction conditions and all, or most, of the atoms from the various reactants contribute to formation of the target compounds. The main advantages of MCRs are their atom economy, eco-friendliness and the fact that it allows to quickly generate structural diversity [40–44].
We recently reported the synthesis of [1, 2, 4]triazolo[3,4-b][1,3,4]thiadiazines through the multi-component reaction (MCR) process [45]. The presence of a hydrazino group in these molecules offers the possibility to convert them into pyrazole moieties. In view of the numerous biological applications of triazoles, pyrazoles and thiadiazines we became interested in the synthesis of the title compounds. Final compounds were subjected to a variety of assays in order to find antiviral and/or antitumoral activity.
Results and discussions
The synthesis of the ( ±)-3-(1H-pyrazol-1-yl)-6,7-dihydro-5H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine derivatives was performed using a two-step, one pot procedure. In order to optimize the chemistry, a model reaction was carried out using 4-amino-3-hydrazino-5-mercapto-1,2,4-triazole 1, acetylacetone 2, 2,3-dimethoxybenzaldehyde 3 and 4-methoxyphenacylbromide 4 as starting materials (Scheme 1). The first step of the reaction was carried out in ethanol as solvent at reflux temperature, in the presence of a catalytic amount of HCl yielding the intermediate 5-(3,5-dimethyl-1H-pyrazol-1-yl)-4-((4-methoxybenzylidene)amino)-4H-1,2,4-triazole-3-thiol [46]. The intermediate was not isolated instead of it 4-methoxyphenacylbromide 4 was added to the reaction mixture. In order to drive the ring closure to form the thiadiazine moiety, various reaction conditions were explored (Table 1). Running this reaction, either at room temperature or at reflux temperature failed to yield the desired product. Upon the addition of an organic base (such as Pyridine, Piperidine or Triethylamine), the desired product was formed. Using triethylamine as base and running the reaction at reflux temperature (entry 4) resulted in the formation of desired compound ( ±)-5a in excellent yield (Table 1).
Scheme 1.
Model reaction. Reaction conditions: a 1 (1 mmol), 2 (1 mmol), 3 (1 mmol), EtOH, HCl (one drop), b 4 (1 mmol), TEA (3 mmol), EtOH, reflux
Table 1.
Screening of the base catalyst
| Entry | Solvent | Base | Temp. (°C) | Time (h) | Yield (%) of ( ±)-5a |
|---|---|---|---|---|---|
| 1 | EtOH | – | 70 | 10 | 0 |
| 2 | EtOH | Pyridine | 70 | 16 | 55 |
| 3 | EtOH | Piperidine | 70 | 12 | 48 |
| 4 | EtOH | Triethylamine | 70 | 11.30 | 92 |
Using this methodology (Scheme 2), a series of compounds was prepared using various benzaldehydes, heterocyclic aldehydes and phenacyl bromides (Table 2). This approach is simple and affords the desired products in yields ranging from 83 to 94%. (Table 3).
Scheme 2.
One-pot, four-component synthesis of ( ±)-3-(1H-pyrazol-1-yl)-6,7-dihydro-5H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine derivatives (5a-t)
Table 2.
Derivatives of ( ±)-3-(1H-pyrazol-1-yl)-6,7-dihydro-5H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine (5a-t)
| Product | R1 | R2 | R3 | R4 | R5 | X | Time (h) | Yield (%) |
|---|---|---|---|---|---|---|---|---|
| 5a | OCH3 | OCH3 | H | H | OCH3 | – | 11.30 | 92 |
| 5b | H | H | CH3 | H | CH3 | – | 11.00 | 91 |
| 5c | H | H | NO2 | H | NO2 | – | 14.30 | 83 |
| 5d | H | OCH3 | H | H | Cl | – | 12.00 | 86 |
| 5e | Br | H | H | H | F | – | 12.30 | 90 |
| 5f | Br | H | H | H | CH3 | – | 11.50 | 92 |
| 5 g | H | H | Cl | H | Br | – | 13.00 | 90 |
| 5 h | H | H | Cl | H | CH3 | – | 12.00 | 93 |
| 5i | H | OCH3 | OH | OCH3 | H | – | 11.40 | 89 |
| 5j | H | F | F | F | CH3 | – | 14.00 | 92 |
| 5 k | H | F | F | F | H | – | 13.30 | 90 |
| 5 l | H | OCH3 | OCH3 | OCH3 | F | – | 13.15 | 88 |
| 5 m | H | OCH3 | OCH3 | OCH3 | H | – | 11.40 | 94 |
| 5n | Cl | H | H | H | OCH3 | – | 14.15 | 86 |
| 5o | OCH3 | H | OCH3 | H | OCH3 | – | 12.00 | 94 |
| 5p | OCH3 | H | OCH3 | H | NO2 | – | 14.00 | 92 |
| 5q | – | – | – | – | OCH3 | O | 14.30 | 87 |
| 5r | – | – | – | – | CH3 | O | 14.15 | 85 |
| 5 s | – | – | – | – | NO2 | S | 15.00 | 89 |
| 5t | – | – | – | – | NO2 | O | 14.50 | 92 |
Table 3.
Hydrogen bonding interactions
| S. no | D–H…A | H…A (Å) | D…A (Å) | D–H…A (°) |
|---|---|---|---|---|
| 1 | N(6)-H(6) … N(2)i | 2.50 | 3.1298 | 130 |
| 2 | C(4)-H(4) … N(4)i | 2.38 | 3.2637 | 150 |
| 3 | C(19)-H(19) … O(1)ii | 2.46 | 3.3727 | 160 |
Symmetry transformations used: (i) ½-x, ½ + y, ½ + z; (ii) -½-x, ½ + y,½-z;
In the present investigation, pyrazole and dihydrothiadiazine skeletons were developed using one-pot, four-component reaction. Initially, hydrazino functional group of compound 1 underwent cyclocondensation with acetylacetone 2 to form pyrazole ring [47]. Then an appropriate amount of different aldehydes 3 and substituted phenacyl bromides 4 were reacted with amine (–NH2) and thiol (–SH) groups of compound 1 respectively by using triethylamine to establish the dihydrothiadiazines (Scheme 3) [48].
Scheme 3.
Plausible mechanism for the synthesis of compounds ( ±)–5a-t
The structures of the final products were confirmed by their spectral data. The FT-IR spectrum of product ( ±)-5b showed a characteristic stretching band at 1681 cm−1 corresponding to the –C=O functional group, whereas the –NH– group appeared at 3135 cm−1. The 1H-NMR spectrum of compound ( ±)-5b showed characteristic peaks, such as two singlets at 2.21 and 2.95 ppm, arising from the two methyl groups on the pyrazole ring. Another two singlets appeared at 2.37 and 2.43 ppm that were assigned to the methyl groups on both phenyl moieties. The two –CH– protons of the dihydrothiadiazine skeleton were visible as two doublets at 5.05 and 5.25 ppm, respectively. The proton of the pyrazole ring showed up as a singlet at 6.00 ppm, whereas the –NH– proton appeared at 7.42 ppm. The remaining aromatic protons appeared in the region of 7.11–7.80 ppm. The 13C-NMR spectrum of compound ( ±)-5b showed peaks at 11.9 and 13.6 ppm for the carbon atoms of two methyl groups on the pyrazole ring at 21.1 and 21.8 ppm for the carbons of two methyl groups on the phenyl moiety. The characteristic carbons of the dihydrothiadiazine skeleton appeared at 44.2 and 59.3 ppm respectively. The pyrazole carbon displayed a peak at 107.8 ppm, whereas the carbonyl peak appeared as the most downfield signal at 193.7 ppm. The remaining aromatic carbons appeared in the range of 127.3 to 151.8 ppm. Mass spectral analysis of compound ( ±)-5b showed a molecular ion peak at m/z 445.
X-ray crystallography
To confirm the structure, crystalline material of compound ( ±)-5 h was isolated, and single crystal X-ray diffraction data were obtained. The compound crystallizes in a monoclinic P21/n space group. The molecular structure of ( ±)–5 h in ORTEP representation is shown in Fig. 2.
Fig. 2.
ORTEP representation of compound ( ±)–5 h
Compound ( ±)–5 h has a 4-methylbenzoyl group and 4-chlorophenyl group on two adjacent chiral centers of the six-membered dihydrothiadiazine ring. The dihydrothiadiazine moiety is fused with a triazole ring, further connected to a pyrazole ring through a carbon–nitrogen single bond. The phenyl rings of 4-methylbenzoyl and 4-chlorophenyl groups are almost perpendicular (79.92° and 82.28° respectively) to the mean plane of the fused six- and five-membered rings. The pyrazole ring attached to triazole makes an angle of 55.59° with the mean plane of the fused six- and five-membered rings. The bond distances and angles are consistent with the structure derived from NMR data. The centrosymmetric space group (P21/n) indicates (Table 4) that the material is a racemic mixture. The unit cell contains two pairs of enantiomers and is connected through non-covalent interactions.
Table 4.
Important crystallographic data for compound ( ±)–5 h
| Compound | ( ±)–5 h |
|---|---|
| Chemical formula | C23 H21 Cl N6 O S |
| Formula weight | 464.97 |
| Crystal system | Monoclinic |
| Space group | P21/n |
| a (Å) | 14.2063(18) |
| b (Å) | 8.4877(11) |
| c (Å) | 20.022(3) |
| α (°) | 90 |
| β (o) | 107.576(5) |
| γ (°) | 90 |
| V (Å3) | 2301.6(5) |
| Z | 4 |
| ρ (g cm−3) | 1.342 |
| μ (mm−1) | 0.285 |
| Reflections collected | 34,696 |
| Reflections unique | 4077 |
| Reflections [I ≥ 2σ(I)] | 4077 |
| Parameters | 289 |
| R1, wR2 [I ≥ 2σ(I)] | 0.0471, 0.1330 |
| R1, wR2 [all data] | 0.0537, 0.1387 |
| GOF on F2 | 1.136 |
| Max./Min. Δρ (e Å−3) | − 0.710 |
Non-covalent intermolecular interactions, such as hydrogen bonding, play an essential role in binding of drugs to their targets, such as DNA or proteins. In this context, the possibility of the presence of non-covalent interactions in the solid state structure of compound ( ±)–5 h was explored. As a result, we were able to identify one N–H … N hydrogen bonding, one C–H … O interaction and one C–H … N interaction (Fig. 3). The interactions and corresponding symmetry transformations are listed in Table 3.
Fig. 3.
Intermolecular Hydrogen bonding interactions of compound ( ±)–5 h in crystal lattice
Biological evaluation
In vitro antiviral screening
Compounds (( ±)–5a-t) were subjected to a broad antiviral screening. At a concentration of 100 µM, no selective antiviral activity was observed for the following viruses: influenza A (H1N1 and H3N2) and influenza B virus (in MDCK cells), respiratory syncytial virus (in HEp-2cells), yellow fever virus (in Huh7 cells), herpes simplex virus type 1 and 2 (in HEL 299 cells). However, a number of derivatives did show antiviral activity against the human corona virus 229E (hCoV-229E) in HEL 299 cells (Table 5). Especially compounds ( ±)–5b and ( ±)–5f displayed promising activity with EC50 values of 4.7 and 3.2 µM, respectively. In addition, both derivatives lacked cytotoxicity for the HEL cells giving rise to favorable selectivity indexes.
Table 5.
Antiviral evaluation of compounds ( ±)–5a–t against hCoV-229E
| Compound | Conc. unit | hCoV-229E (HEL cells) | |
|---|---|---|---|
| CC50 | EC50 | ||
| 5b | µM | 81.5 | 4.7 ± 0.5 (*) |
| 5c | µM | > 100 | 24.4 |
| 5e | µM | > 100 | > 100 |
| 5f | µM | > 100 | 3.2 ± 1.8 (*) |
| 5 g | µM | > 100 | > 100 |
| 5 h | µM | > 100 | 38.0 |
| 5j | µM | 23.8 | > 100 |
| 5 k | µM | > 100 | > 100 |
| 5 m | µM | > 100 | 95.7 |
| 5n | µM | > 100 | > 100 |
| 5p | µM | > 100 | > 100 |
| 5q | µM | < 0.8 | > 100 |
| 5r | µM | > 100 | > 100 |
| 5 s | µM | > 100 | > 100 |
| 5t | µM | > 100 | > 100 |
| UDA | µg/ml | > 100 | 2.1 |
(*)Mean value of three independent experiments ± SEM
In vitro antitumoral screening
To investigate their anti-cancer potential, compounds 5a-t were tested in vitro for their anti-proliferative properties, using a real-time IncuCyteproliferation assay against an array of solid and hematological cancers including LN-229 (glioblastoma), Capan-1 (pancreatic adenocarcinoma), HCT-116 (colorectal carcinoma), NCI-H460 (lung carcinoma), DND-41 (acute lymphoblastic leukemia), HL-60 (acute myeloid leukemia), K-562 (chronic myeloid leukemia) and Z-138 (non-Hodgkin lymphoma) cell lines. Docetaxel (a microtubule depolymerisation inhibitor) and staurosporine (STS, a pan-kinase inhibitor) were used as positive controls. From this screening campaign, two derivatives (compounds 5j and 5q) emerged that showed low µM activity against the different cell lines (Table 6).
Table 6.
Antitumoral evaluation of compounds from ( ±)–5a-t. IC50
| Compound | IC50 (µM) | |||||||
|---|---|---|---|---|---|---|---|---|
| LN-229 | Capan-1 | HCT-116 | NCI-H460 | DND-41 | HL-60 | K-562 | Z-138 | |
| 5b | 47.1 | 57.5 | 67.8 | > 100 | 39.3 | 50.9 | 10.4 | 48.4 |
| 5c | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 |
| 5e | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 |
| 5f | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 |
| 5 g | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 |
| 5 h | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 |
| 5j* | 2.7 ± 0.2 | 2.3 ± 0.2 | 2.5 ± 0.09 | 56.0 | 2.4 ± 0.4 | 13.0 ± 2.8 | 3.4 ± 0.2 | 1.9 ± 0.03 |
| 5 k | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 |
| 5 m | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 |
| 5n | 68.3 | 63.1 | > 100 | > 100 | 91.7 | 71.2 | 53.2 | 53.9 |
| 5p | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 |
| 5q* | 0.7 ± 0.09 | 1.1 ± 0.7 | 1.0 ± 0.4 | 2.5 ± 0.2 | 0.6 ± 0.2 | 2.0 ± 0.4 | 2.3 ± 1.6 | 0.4 ± 0.005 |
| 5r | 43.9 | 54.3 | 69.0 | 47.0 | 70.2 | 54.0 | 23.5 | 50.2 |
| 5 s | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 | > 100 |
| 5t | 62.7 | > 100 | > 100 | > 100 | > 100 | 74.5 | 79.3 | 49.5 |
| Docetaxel* | 0.0087 ± 0.0004 | 0.0042 ± 0.0021 | 0.0009 ± 0.0008 | 0.0038 ± 0.0029 | 0.0033 ± 0.0014 | 0.0023 ± 0.0003 | 0.0037 ± 0.0003 | 0.0011 ± 0.0008 |
| STS* | 0.0229 ± 0.0021 | 0.0007 ± 0.0002 | 0.0004 ± 0.0001 | 0.00010 ± 0.0000 | 0.0015 ± 0.0004 | 0.0043 ± 0.0022 | 0.0074 ± 0.0017 | 0.0224 ± 0.0074 |
*Mean value of two independent experiments ± SEM
Because of the promising antitumoral profile of compounds ( ±)–5j and ( ±)–5q, their apoptogenic potential in non-cancerous peripheral blood mononuclear cells (PBMCs) was determined as counter screening. The activation of the executioner caspases-3 and -7 normally precedes the manifestation of apoptosis as massive DNA fragmentation. Therefore, the caspase-3/7 Green reagent was added to the PBMCs, which are also treated with different concentrations of compounds ( ±)–5j and ( ±)–5q. When activated caspase 3 or 7 are intracellularly present, they will cleave the Caspase-3/7 Green Reagent at the DEVD motif. This results in the release of a DNA binding dye that fluorescently labels nuclear DNA of apoptic cells. In addition, in order to distinguish dead cells from live cells, a propidium iodide (PI) staining was carried out. As can be derived from Fig. 4, only very high concentrations of compounds ( ±)–5j and ( ±)–5q (100 µM) give rise to a small increase in the number of apoptotic and dead cells. Overall, these data indicate that compounds ( ±)–5j and ( ±)–5q did not inhibit the viability of normal PBMCs and demonstrate selectivity toward cancer cells over normal cells (Fig. 4).
Fig. 4.
Analysis of apoptosis induction by compound–5j (left) and ( ±)–5q (right) in PBMC originating from two healthy donors
Despite their promising antitumoral profile, the exact molecular target of compounds ( ±)-5j and ( ±)-5q remained elusive. In order to assess whether they interact with tubulin, an immune fluorescence analysis of tubulin in HEp-2 cells treated for 3 h with compounds ( ±)-5j and ( ±)-5q was performed, and compared to DMSO (vehicle control) and to vincristine (a known tubulin polymerization inhibitor, used as positive control). It can be clearly observed that both compounds ( ±)-5j and ( ±)-5q inhibit the polymerization of tubulin in a dose-dependent manner (Fig. 5).
Fig. 5.
Immune fluorescence staining of alpha-tubulin in HEp-2 cells: a Representative images of normal alpha-tubulin after treatment with DMSO (top) or typical phenotype after treatment with vincristine (bottom), b Treatment with compounds ( ±)–5j and ( ±)–5q. Green: alpha-tubulin, blue: DAPI. Scale bar: 25 µM
Conclusion
The synthesis of a new series of ( ±)-3-(1H-pyrazol-1-yl)-6,7-dihydro-5H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine derivatives was carried out in an excellent yields via a one-pot, four-component method using readily available starting materials. The reactions proceeds in such a way with high atom economy, leading to the formation of one C=N, two C–N, one C–C, and one C–S bonds in a single operation, giving multi-annulated products. All the final compounds were tested for their antiviral and antitumoral activity. It was demonstrated that subtle structural modifications on the phenyl moieties allowed to tune the biological properties of the compounds. Among the newly synthesized compounds, a number of derivatives show promising antiviral activity against the hCoV-229E, whereas other derivatives exhibited cytotoxicity in various cancer cell lines. In addition, it was demonstrated that the antitumoral activity of these compounds is caused by inhibition of tubulin polymerization.
Experimental
General
All the reactants, reagents and solvents were pure, purchased from commercial sources and used without further purification. All the synthesized compounds were preliminarily confirmed by monitoring using TLC plates (E, Merck, Mumbai, India) in the UV-light chamber. A “Stuart SMP30” programmable melting point instrument (Bibby Scientific Ltd. U.K.) was used to record the melting points of the synthesized compounds. FT-IR spectra of the newly synthesized compounds in KBr-pellets were recorded on a PerkinElmer 100S FT-IR spectrophotometer. The 1H- and the 13C-NMR chemical shift values were determined for the compounds on Avance-III Bruker WM-400 MHz spectrometer in δ ppm. Tetramethylsilane (TMS) acts as reference standard for the chemical shifts. Suitable deuterated solvents like CDCl3 and DMSO-d6 were used as solvent for the various compounds to record 1H- and 13C-NMR spectra. Molecular ion peaks were recorded as m/z, ESI-Mass spectra on a PerkinElmer spectrometer performing at 12.5 eV. Carlo Erba EA 1108 CHNS-O automatic analyzer was used for the elemental analysis.
General procedure for the synthesis of ( ±)-(3-(3,5-dimethyl-1H-pyrazol-1-yl)-6-phenyl-6,7-dihydro-5H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)(phenyl)methanones (5a-t).
A mixture of 4-amino-5-hydrazino-4H-[1, 2, 4] triazole-3-thiol 1 (1 mmol), acetyl acetone (ACAC) 2 (1 mmol) and appropriate aromatic aldehydes/heterocyclic aldehydes 3 (1 mmol) was taken sequentially in 5 mL of dry ethanol containing drop of Conc. HCl. The reaction mixture was refluxed for 5–7 h by monitoring TLC. After completion of reaction, to the reaction mixture substituted phenacyl bromides 4 (1 mmol) and triethylamine (TEA) (3 mmol) were added and one drop of HCl was neutralized by one mole of TEA. Then the reaction was continued under the reflux for 6–8 h by monitoring TLC (CHCl3:CH3OH = 95:5). The reaction mixture was cooled to room temperature, diluted with water and the solid separated was filtered. The final products were recrystallized from 6–8 mL ethanol.
( ±)-(6-(2,3-Dimethoxyphenyl)-3-(3,5-dimethyl-1H-pyrazol-1-yl)-6,7-dihydro-5H[1,2,4]triazole [3,4-b][1,3,4]thiadiazin-7-yl)(4-methoxyphenyl)methanone (5a)
Light yellow color solid; yield 92%; m.p.: 192–194 °C; IR (KBr, ʋmax/cm−1): 3211 (NH), 1668 (C=O); 1H-NMR (400 MHz, CDCl3, δ ppm): 2.24 (s, 3H, CH3), 2.40 (s, 3H, CH3), 3.87 (s, 6H, OCH3), 3.90 (s, 3H, OCH3), 5.28 (unresolved doublet, 2H, CH), 6.00 (s, 1H, CH of pyrazole ring), 6.68 (d, 1H, J = 7.6 Hz, Ar–H), 6.88 (d, 1H, J = 8.0 Hz, Ar–H), 6.94 (s, 1H, NH), 6.97 (d, 2H, J = 8.4 Hz, Ar–H), 7.11 (d, 1H, J = 8.0 Hz, Ar–H), 7.94 (d, 2H, J = 8.8 Hz, Ar–H); 13C-NMR (100 MHz, CDCl3, δ ppm): 11.7, 13.7, 42.6, 54.9, 55.7, 55.8, 61.0, 107.7, 112.9, 114.3, 119.7, 124.4, 127.4, 129.4, 130.3, 130.8, 131.2, 142.9, 146.1, 151.8, 152.6, 164.6, 193.2; ESI–MS m/z: 507 [M + H]+; Analytical calculated formulae C25H26N6O4S: C, 59.27; H, 5.17; N, 16.59; S, 6.33; Found: C, 59.22; H, 5.22; N, 16.53; S, 6.30.
( ±)-(3-(3,5-Dimethyl-1H-pyrazol-1-yl)-6-(p-tolyl)-6,7-dihydro-5H-[1,2,4]triazolo[3,4-b][1,3,4] thiadiazin-7-yl)(p-tolyl)methanone (5b)
White solid; yield 91%; m.p.: 194–196 °C; IR (KBr, ʋmax/cm−1): 3135 (NH), 1681 (C=O); 1H-NMR (400 MHz, CDCl3, δ ppm): 2.22 (s, 3H, CH3), 2.30 (s, 3H, CH3), 2.38 (s, 3H, CH3), 2.43 (s, 3H, CH3), 5.05 (unresolved doublet, 1H, CH), 5.25 (d, 1H, J = 5.2 Hz, CH), 6.00 (s, 1H, CH of pyrazole ring), 7.11 (d, 2H, J = 8.0 Hz, Ar–H), 7.29 (d, 4H, J = 7.2 Hz, Ar–H), 7.42 (s, 1H, NH), 7.80 (d, 2H, J = 8.0 Hz, Ar–H); 13C-NMR (100 MHz, CDCl3, δ ppm): 11.9, 13.6, 21.1, 21.8, 44.2, 59.3, 107.8, 127.3, 128.8, 129.7, 129.8, 132.0, 132.7, 138.8, 141.3, 143.1, 145.6, 145.7, 151.8, 193.7; ESI–MS m/z: 445 [M + H]+; Analytical calculated formulae C24H24N6OS: C, 64.84; H, 5.44; N, 18.90; S, 7.21; Found: C, 64.89; H, 5.40; N, 18.85; S, 7.18.
( ±)-(3-(3,5-Dimethyl-1H-pyrazol-1-yl)-6-(4-nitrophenyl)-6,7-dihydro-5H-[1,2,4]triazolo[3,4-b][1,3,4] thiadiazin-7-yl)(4-nitrophenyl)methanone (5c)
Yellow solid; yield 83%; m.p.: 242–244 °C; IR (KBr, ʋmax/cm−1): 3302 (NH), 1614 (–C=O); 1H-NMR (400 MHz, CDCl3, δ ppm): 2.16 (s, 3H, CH3), 2.44 (s, 3H, CH3), 5.05 (d, 1H, J = 6.0 Hz, CH), 5.20 (d, 1H, J = 6.0 Hz, CH), 6.00 (s, 1H, CH of pyrazole ring), 7.30 (d, 2H, J = 8.4 Hz, Ar–H), 7.38 (d, 2H, J = 8.4 Hz, Ar–H), 7.65 (d, 2H, J = 8.1 Hz, Ar–H), 7.73 (s, 1H, NH), 7.77 (d, 2H, J = 8.4 Hz, Ar–H); 13C-NMR (100 MHz, CDCl3, δ ppm): 12.0, 13.5, 44.1, 59.1, 107.9, 128.9, 129.0, 129.2, 129.9, 131.9, 134.3, 134.9, 141.0, 143.1, 145.5, 146.0, 151.8, 193.5; ESI–MS m/z: 507 [M + H]+; Analytical calculated formulae C22H18N8O5S: C, 52.17; H, 3.58; N, 22.12; S, 6.33; Found: C, 52.23; H, 3.54; N, 22.17; S, 6.30.
( ±)-(4-Chlorophenyl)(3-(3,5-dimethyl-1H-pyrazol-1-yl)-6-(3-methoxyphenyl)-6,7-dihydro-5H-[1,2,4]triazolo[3,4-b][1,3,4][1,3,4]thiadiazin-7-yl)methanone (5d)
Cream color solid; yield 86%; m.p.: 188–190 °C; IR (KBr, ʋmax/cm−1): 3138 (NH), 1692 (C=O); 1H-NMR (400 MHz, CDCl3, δ ppm): 2.19 (s, 3H, CH3), 2.41 (s, 3H, CH3), 3.74 (s, 3H, OCH3), 5.04 (t, 1H, J = 4.0 Hz, CH), 5.25 (d, 1H, J = 4.4 Hz, CH), 6.00 (s, 1H, CH of pyrazole ring), 6.83 (d, 1H, J = 6.8 Hz, Ar–H), 6.96 (s, 1H, Ar–H), 6.98 (d, 1H, J = 6.4 Hz, Ar–H), 7.23 (t, 1H, J = 6.4 Hz, Ar–H), 7.47 (d, 2H, J = 6.4 Hz, Ar–H), 7.58 (s, 1H, NH), 7.84 (d, 2H, J = 6.8 Hz, Ar–H); 13C-NMR (100 MHz, CDCl3, δ ppm): 12.0, 13.6, 44.9, 55.3, 59.8, 107.9, 113.3, 114.4, 119.4, 129.5, 130.1, 130.2, 132.9, 137.1, 140.9, 141.2, 143.2, 145.5, 151.8, 160.0 192.9; ESI–MS m/z: 481 [M + H]+; Analytical calculated formulae C23H21ClN6O2S: C, 57.44; H, 4.40; N, 17.47; S, 6.67; Found: C, 57.48; H, 4.45; N, 17.42; S, 6.62.
( ±)-(6-(2-Bromophenyl)-3-(3,5-dimethyl-1H-pyrazol-1-yl)-6,7-dihydro-5H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)(4-fluorophenyl)methanone (5e)
Golden yellow color solid; yield 90%; m.p.: 195–197 °C; IR (KBr, ʋmax/cm−1): 3138 (NH), 1692 (C=O); 1H-NMR (400 MHz, CDCl3, δ ppm): 2.15 (s, 3H, CH3), 2.48 (s, 3H, CH3), 5.22 (d, 1H, J = 4.0 Hz, CH), 5.50 (t, 1H, J = 4.8 Hz, CH), 5.99 (s, 1H, CH of pyrazole ring), 7.17 (s, 1H, NH), 7.20 (d, 2H, J = 8.4 Hz, Ar–H), 7.24 (d, 1H, J = 2.0 Hz, Ar–H), 7.59 (d, 1H, J = 7.6 Hz, Ar–H), 7.78 (d, 1H, J = 5.6 Hz, Ar–H), 8.01 (dd, 2H, J = 8.8 Hz, J = 5,2 Hz, Ar–H); 13C-NMR (100 MHz, CDCl3, δ ppm): 11.9, 13.3, 43.1, 58.3, 107.8, 116.3, 116.5, 123.2, 128.1, 128.6, 130.2, 131.7, 131.8, 133.4, 136.4, 140.0, 142.9, 145.5, 151.7, 166.2, 167.8 192.5; ESI–MS m/z: 515 [M + 2]+; Analytical calculated formulae C22H18BrFN6OS: C, 51.47; H, 3.53; N, 16.37; S, 6.25; Found: C, 51.42; H, 3.57; N, 16.32; S, 6.20.
( ±)-(6-(2-Bromophenyl)-3-(3,5-dimethyl-1H-pyrazol-1-yl)-6,7-dihydro-5H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)(p-tolyl)methanone (5f)
Lemon yellow color solid; yield 92%; m.p.: 201–203 °C; IR (KBr, ʋmax/cm−1): 3148 (NH), 1673 (C=O); 1H-NMR (400 MHz, CDCl3, δ ppm): 2.20 (s, 3H, CH3), 2.44 (s, 3H, CH3), 2.46 (s, 3H, CH3), 5.22 (d, 1H, J = 4.0 Hz, CH-), 5.49 (t, 1H, J = 4.8 Hz, CH), 6.00 (s, 1H, CH of pyrazole ring), 7.19 (t, 2H, J = 8.0 Hz, Ar–H), 7.23 (s, 1H, NH), 7.31 (d, 2H, J = 8.0 Hz, Ar–H), 7.58 (d, 1H, J = 7.6 Hz, Ar–H), 7.65 (d, 1H, J = 5.2 Hz, Ar–H), 7.86 (d, 2H, J = 8.0 Hz, Ar–H); 13C-NMR (100 MHz, CDCl3, δ ppm): 11.9, 13.5, 21.8, 42.9, 57.8, 107.8, 123.0, 128.1, 128.6, 128.9, 129.9, 130.2, 131.7, 133.4, 136.6 140.1, 142.9, 145.6, 145.7, 151.8, 193.7; ESI–MS m/z: 511 [M + 2]+; Analytical calculated formulae C23H21BrN6OS: C, 54.23; H, 4.16; N, 16.50; S, 6.29; Found: C, 54.28; H, 4.21; N, 16.44; S, 6.33.
( ±)-(4-Bromophenyl)(6-(4-chlorophenyl)-3-(3,5-dimethyl-1H-pyrazol-1-yl)-6,7-dihydro-5H- triazolo[3,4-b][1,3,4]thiadiazin-7-yl)methanone (5g)
White solid; yield 90%; m.p.: 205–207 °C; IR (KBr, ʋmax/cm−1): 3291 (NH), 1688 (C=O); 1H-NMR (400 MHz, CDCl3, δ ppm): 2.16 (s, 3H, –CH3), 2.44 (s, 3H, CH3), 5.05 (dd, 1H, J = 6.0 Hz, J = 3.6 Hz, CH–), 5.2 (d, 1H, J = 6.0 Hz, CH), 6.00 (s, 1H, CH of pyrazole ring), 7.30 (d, 2H, J = 8.4 Hz, Ar–H), 7.38 (d, 2H, J = 8.4 Hz, Ar–H), 7.65 (d, 2H, J = 8.1 Hz, Ar–H), 7.72 (s, 1H, NH), 7.77 (d, 2H, J = 8.4 Hz, Ar–H); 13C-NMR (100 MHz, CDCl3, δ ppm): 12.0, 13.5, 44.9, 59.5, 107.9, 129.0, 129.3, 132.1, 130.2 132.6, 133.2, 134.2, 135.1, 140.6, 143.1, 145.3, 151.8, 192.8; ESI–MS m/z: 531 [M + 2]+; Analytical calculated formulae C22H18BrClN6OS: C, 49.87; H, 3.42; N, 15.86; S, 6.05; Found: C, 49.84; H, 3.48; N, 15.83; S, 6.12.
( ±)-(6-(4-Chlorophenyl)-3-(3,5-dimethyl-1H-pyrazol-1-yl)-6,7-dihydro-5H-[1,2,4]triazolo[3,4-b] [1,3,4]thiadiazin-7-yl)(p-tolyl)methanone (5 h)
White solid; yield 93%; m.p.: 214–216 °C; IR (KBr, ʋmax/cm−1): 3219 (NH), 1675 (C=O); 1H-NMR (400 MHz, CDCl3 + DMSO-d6, δ ppm): 2.25 (s, 3H, CH3), 2.31 (s, 3H, CH3), 2.44 (s, 3H, CH3), 3.21 (s, 1H, NH), 4.99 (unresolved singlet, 1H, CH), 5.69 (d, 1H, J = 5.2 Hz, CH), 6.06 (s, 1H, CH of pyrazole ring), 7.19 (d, 1H, J = 7.2 Hz, Ar–H), 7.28 (d, 1H, J = 6.4 Hz, Ar–H), 7.33 (d, 2H, J = 7.6 Hz, Ar–H), 7.47 (s, 2H, Ar–H), 7.90 (s, 2H, Ar–H); 13C-NMR (100 MHz, CDCl3 + DMSO-d6, δ ppm): 11.4, 13.7, 21.8, 42.5, 58.2, 107.6, 128.9, 129.1, 129.3, 129.8, 132.2, 133.9, 135.2, 141.8, 142.8, 145.6, 146.6, 151.4, 194.3; ESI–MS m/z: 465 [M + H]+; Analytical calculated formulae C23H21ClN6OS: C, 59.41; H, 4.55; N, 18.07; S, 6.90; Found: C, 59.45; H, 4.51; N, 18.10; S, 6.85.
( ±)-(3-(3,5-Dimethyl-1H-pyrazol-1-yl)-6-(4-hydroxy-3,5-dimethoxyphenyl)-6,7-dihydro-5H- triazolo[3,4-b][1,3,4]thiadiazin-7-yl)(phenyl)methanone (5i)
Green solid; yield 89%; m.p.: 196–198 °C; IR (KBr, ʋmax/cm−1): 3435 (OH), 3134 (NH), 1653 (C=O); 1H-NMR (400 MHz, CDCl3 + DMSO-d6, δ ppm): 2.21 (s, 3H, CH3), 2.25 (s, 3H, CH3), 3.71 (s, 6H, OCH3), 4.80 (t, 1H, J = 6.8 Hz, CH), 5.86 (d, 1H, J = 6.0 Hz, CH), 6.11 (s, 1H, CH of pyrazole ring), 6.35 (s, 1H, OH), 6.77 (s, 2H, Ar–H), 7.07 (s, 1H, NH), 7.54 (t, 2H, J = 8.0 Hz, Ar–H), 7.67 (t, 1H, J = 7.2 Hz, Ar–H), 8.00 (d, 2H, J = 7.2 Hz, Ar–H); 13C-NMR (100 MHz, CDCl3, δ ppm): 11.9, 13.5, 45.4, 56.2, 60.8, 104.8, 107.8, 128.7, 129.1, 131.0, 134.5, 134.7, 138.4, 141.5, 143.2, 145.4, 151.7, 153.5, 194.1; ESI–MS m/z: 493 [M + H]+; Analytical calculated formulae C24H24N6O4S: C, 58.52; H, 4.91; N, 17.06; S, 6.51; Found: C, 58.57; H, 4.94; N, 17.10; S, 6.47.
( ±)-(3-(3,5-Dimethyl-1H-pyrazol-1-yl)-6-(3,4,5-trifluorophenyl)-6,7-dihydro-5H-[1,2,4]triazole [3,4-b][1,3,4]thiadiazin-7-yl)(p-tolyl)methanone (5j)
White solid; yield 92%; m.p.: 215–217 °C; IR (KBr, ʋmax/cm−1): 3219 (NH), 1674 (C=O); 1H-NMR (400 MHz, CDCl3, δ ppm): 2.19 (s, 3H, CH3), 2.43 (s, 3H, CH3), 2.50 (s, 3H, CH3), 3.48 (s, 1H, NH), 5.035 (t, 1H, J = 8.0 Hz, CH), 5.48 (d, 1H, J = 8.0 Hz, CH), 6.00 (s, 1H, CH of pyrazole ring), 6.67 (t, 2H, J = 8.4 Hz, Ar–H), 7.30 (d, 2H, J = 8.4 Hz, Ar–H), 7.82 (d, 2H, J = 8.0 Hz, Ar–H); 13C-NMR (100 MHz, CDCl3, δ ppm): 11.9, 13.5, 21.8, 44.1, 53.1, 101.3, 107.9, 127.5, 128.9, 129.9, 129.8, 131.6, 141.3, 143.2, 145.6, 146.1, 151.8, 160.0, 192.2; ESI–MS m/z: 485 [M + H]+; Analytical calculated formulae C23H19F3N6OS: C, 57.02; H, 3.95; N, 17.35; S, 6.62; Found: C, 57.17; H, 3.99; N, 17.39; S, 6.62.
( ±)-(3-(3,5-Dimethyl-1H-pyrazol-1-yl)-6-(3,4,5-trifluorophenyl)-6,7-dihydro-5H-[1,2,4]triazole [3,4-b][1,3,4]thiadiazin-7-yl)(phenyl)methanone (5 k)
Light yellow color solid; yield 90%; m.p.: 182–184 °C; IR (KBr, ʋmax/cm−1): 3207 (NH), 1681 (C=O); 1H-NMR (400 MHz, CDCl3, δ ppm): 2.15 (s, 3H, CH3), 2.49 (s, 3H, CH3), 5.34 (t, 1H, J = 8.0 Hz, CH–), 5.56 (d, 1H, J = 8.4 Hz, CH), 5.99 (s, 1H, CH of pyrazole ring), 6.67 (t, 2H, J = 8.4 Hz, Ar–H), 7.15 (s, 1H, NH), 7.51 (t, 2H, J = 7.6 Hz, Ar–H), 7.64 (t, 1H, J = 7.2 Hz, Ar–H), 7.94 (d, 2H, J = 7.6 Hz, Ar–H); 13C-NMR (100 MHz, CDCl3, δ ppm): 11.9, 13.4, 44.3, 53.2, 101.3, 107.9, 127.5, 128.9, 129.1, 129.2, 130.4, 134.8, 134.9, 141.2, 143.2, 145.6, 151.8, 192.7; ESI–MS m/z: 471 [M + H]+; Analytical calculated formulae C22H17F3N6OS: C, 56.16; H, 3.64; N, 17.86; S, 6.82; Found: C, 56.12; H, 3.60; N, 17.90; S, 6.87.
( ±)-(3-(3,5-Dimethyl-1H-pyrazol-1-yl)-6-(3,4,5-trimethoxyphenyl)-6,7-dihydro-5H-triazole[3,4-b][1,3,4]thiadiazin-7-yl)(4-fluorophenyl)methanone (5 l)
White solid; yield 88%; m.p.: 196–198 °C; IR (KBr, ʋmax/cm−1): 3211 (NH), 1668 (C = O); 1H-NMR (400 MHz, CDCl3 + DMSO-d6, δ ppm): 2.18 (s, 3H, CH3), 2.22 (s, 3H, CH3), 3.69 (s, 3H, OCH3), 3.70 (s, 3H, OCH3), 3.87 (s, 3H, OCH3), 4.45 (t, 1H, J = 6.8 Hz, CH), 5.83 (d, 1H, J = 6.4 Hz, CH), 6.15 (s, 1H, CH of pyrazole ring), 6.87 (s, 1H, Ar–H), 6.97 (s, 1H, Ar–H), 7.07 (s, 1H, NH), 7.12 (d, 2H, J = 7.2 Hz, Ar–H), 8.01 (d, 2H, J = 8.4 Hz, Ar–H); 13C-NMR (100 MHz, CDCl3, δ ppm): 11.7, 13.7, 42.5, 54.9, 55.7, 55.8, 61.0, 107.7, 112.9, 114.3, 119.7, 124.4, 127.4, 129.4, 131.2, 142.9, 151.7, 152.6, 164.6, 193.2;ESI–MS m/z: 525 [M + H]+; Analytical calculated formulae C25H25FN6O4S: C, 57.24; H, 4.80; N, 16.02; S, 6.11; Found: C, 57.20; H, 4.85; N, 16.17; S, 6.15.
( ±)-(3-(3,5-Dimethyl-1H-pyrazol-1-yl)-6-(3,4,5-trimethoxyphenyl)-6,7-dihydro-5H-[1,2,4]triazole [3,4-b][1,3,4]thiadiazin-7-yl)(phenyl)methanone (5m)
Golden yellow color solid; yield 94%; m.p.: 192–194 °C; IR (KBr, ʋmax/cm−1): 3129 (NH), 1680 (C=O); 1H-NMR (400 MHz, CDCl3, δ ppm): 2.19 (s, 3H, CH3), 2.39 (s, 3H, CH3), 3.48 (s, 6H, OCH3), 3.78 (s, 3H, OCH3), 5.00 (t, 1H, J = 5.2 Hz, CH), 5.31 (d, 1H, J = 5.6 Hz, CH), 6.00 (s, 1H, CH of pyrazole ring), 6.66 (s, 2H, Ar–H), 7.50 (t, 2H, J = 7.6 Hz, Ar–H), 7.59 (s, 1H, NH), 7.63 (t, 1H, J = 7.6 Hz, Ar–H), 7.90 (d, 2H, J = 7.6 Hz, Ar–H); 13C-NMR (100 MHz, CDCl3, δ ppm): 11.9, 13.5, 45.4, 56.2, 60.6, 60.8, 104.8, 107.8, 128.7, 129.1, 131.0, 134.5, 134.7, 138.4, 141.5, 143.2, 145.4, 151.7, 153.5, 194.1; ESI–MS m/z: 507 [M + H]+; Analytical calculated formulae C25H26N6O4S: C, 59.27; H, 5.17; N, 16.59; S, 6.33; Found: C, 59.24; H, 5.20; N, 16.54; S, 6.38.
( ±)-(6-(2-Chlorophenyl)-3-(3,5-dimethyl-1H-pyrazol-1-yl)-6,7-dihydro-5H-[1,2,4]triazolo[3,4-b][1,3,4] thiadiazin-7-yl)(4-methoxyphenyl)methanone (5n)
White solid; yield 86%; m.p.: 198–200 °C; IR (KBr, ʋmax/cm−1): 3143 (NH), 1671 (C=O); 1H-NMR (400 MHz, CDCl3, δ ppm): 2.21 (s, 3H, CH3), 2.45 (s, 3H, CH3), 3.90 (s, 3H, OCH3), 5.18 (d, 1H, J = 4.0 Hz, CH), 5.50 (t, 1H, J = 4.4 Hz, CH), 6.00 (s, 1H, CH of pyrazole ring), 6.98 (d, 2H, J = 8.8 Hz, Ar–H), 7.16–7.23 (m, 2H, Ar–H), 7.29 (s, 1H, NH), 7.40 (d, 1H, J = 8.0 Hz, Ar–H), 7.60 (d, 1H, J = 4.8 Hz, Ar–H), 7.94 (d, 2H, J = 8.4 Hz, Ar–H); 13C-NMR (100 MHz, CDCl3, δ ppm): 12.0, 13.5, 21.8, 44.1, 59.1, 107.9, 128.9, 129.0, 129.2, 129.9, 131.9, 134.3, 134.9, 141.0, 143.1, 145.5, 145.9, 151.8, 193.5; ESI–MS m/z: 481 [M + H]+; Analytical calculated formulae C23H21ClN6O2S: C, 57.44; H, 4.40; N, 17.47; S, 6.67; Found: C, 57.40; H, 4.45; N, 17.1; S, 6.62.
( ±)-(6-(2,4-Dimethoxyphenyl)-3-(3,5-dimethyl-1H-pyrazol-1-yl)-6,7-dihydro-5H-[1,2,4]triazole [3,4-b][1,3,4]thiadiazin-7-yl)(4-methoxyphenyl)methanone (5o)
Yellow solid; yield 94%; m.p.: 150–152 °C; IR (KBr, ʋmax/cm−1): 3129 (NH), 1680 (C=O); 1H-NMR (400 MHz, DMSO-d6, δ ppm): 2.19 (s, 3H, CH3), 2.22 (s, 3H, CH3), 3.69 (s, 3H, OCH3), 3.70 (s, 3H, OCH3), 3.87 (s, 3H, OCH3), 4.45 (t, 1H, J = 6.8 Hz, CH), 5.83 (d, 1H, J = 6.4 Hz, CH), 6.16 (s, 1H, CH of pyrazole ring), 6.86 (d, 1H, J = 8.4 Hz, Ar–H), 6.98 (d, 1H, J = 8.4 Hz, Ar–H), 7.07 (s, 1H, NH), 7.10 (d, 2H, J = 8.0 Hz, Ar–H), 7.12 (s, 1H, Ar–H), 8.01 (d, 2H, J = 8.4 Hz, Ar–H); 13C-NMR (100 MHz, CDCl3, δ ppm): 11.7, 13.7, 42.6, 54.9, 55.7, 55.8, 61.0, 107.7, 112.9, 114.3, 119.7, 124.4, 127.4, 129.4, 130.3, 130.8, 131.2, 142.9, 146.1, 151.8, 152.6, 164.6, 193.2; ESI–MS m/z: 507 [M + H]+; Analytical calculated formulae C25H26N6O4S: C, 59.27; H, 5.17; N, 16.59; S, 6.33; Found: C, 59.24; H, 5.14; N, 16.63; S, 6.30.
( ±)-(6-(2,4-dimethoxyphenyl)-3-(3,5-dimethyl-1H-pyrazol-1-yl)-5H-[1,2,4]triazolo[3,4-b][1,3,4] thiadiazin-7-yl)(4-nitrophenyl)methanone (5p)
Yellow solid; yield 88%; m.p.: 236–238 °C; IR (KBr, ʋmax/cm−1): 3135 (NH), 1681 (C=O); 1H-NMR (400 MHz, CDCl3, δ ppm): 2.35 (s, 3H, CH3), 2.42 (s, 3H, CH3), 3.79 (s, 3H, OCH3), 3.88 (s, 3H, OCH3), 6.08 (s, 1H, CH of pyrazole ring), 6.48 (s, 1H, Ar–H), 6.62 (dd, 1H, J = 8.4 Hz, J = 6.4 Hz, Ar–H), 7.27 (s, 1H, NH), 7.43 (d, 1H, J = 8.8 Hz, Ar–H), 7.95 (d, 2H, J = 8.8 Hz, Ar–H), 8.31 (d, 2H, J = 8.8 Hz, Ar–H); 13C-NMR (100 MHz, CDCl3, δ ppm): 11.7, 13.7, 55.6, 55.7, 98.5, 104.7, 108.1, 112.9, 114.6, 123.9, 131.0, 131.2, 138.3, 141.2, 143.6, 146.5, 149.4, 152.4, 16.2, 159.1, 163.3, 196.0; Analytical calculated formulae C24H21N7O5S: C, 55.48; H, 4.07; N, 18.87; S, 6.17; Found: C, 55.43; H, 4.02; N, 18.92; S, 6.21.
( ±)-(3-(3,5-Dimethyl-1H-pyrazol-1-yl)-6-(furan-2-yl)-6,7-dihydro-5H-[1,2,4]triazolo[3,4-b][1,3,4] thiadiazin-7-yl)(4-methoxyphenyl)methanone (5q)
Brown solid; yield 87%; m.p.: 152–154○C; IR (KBr, ʋmax/cm−1): 3143 (NH), 1671 (C = O); 1H-NMR (400 MHz, CDCl3, δ ppm): 2.30 (s, 3H, CH3), 2.34 (s, 3H, CH3), 3.92 (s, 3H, OCH3), 5.23 (unresolved singlet, 2H, CH and CH), 6.03 (s, 1H, CH of pyrazole ring), 6.30 (s, 1H, CH-), 6.32 (s, 1H, CH), 7.02 (d, 3H, J = 8.8 Hz, Ar–H), 7.35 (s, 1H, NH), 7.94 (d, 2H, J = 8.4 Hz, Ar–H); ESI–MS m/z 437 [M + H]+; Analytical calculated formulae C21H20N6O3S: C, 57.79; H, 4.62; N, 19.25; S, 7.35; Found: C, 57.83; H, 4.66; N, 19.21; S, 7.31.
( ±)-(3-(3,5-Dimethyl-1H-pyrazol-1-yl)-6-(furan-2-yl)-6,7-dihydro-5H-[1,2,4]triazolo[3,4-b] [1,3,4]thiadiazin-7-yl)(p-tolyl)methanone (5r)
Brown solid; yield 85%; m.p.: 149–151○C; IR (KBr, ʋmax/cm−1): 3204 (NH), 1666 (C = O); 1H-NMR (400 MHz, CDCl3, δ ppm): 2.30 (s, 3H, CH3), 2.34 (s, 3H, CH3), 2.46 (s, 3H, CH3), 5.26 (unresolved singlet, 2H, CH-), 6.03 (s, 1H, CH of pyrazole ring), 6.31 (d, 2H, J = 8.0 Hz, Ar–H), 7.03 (s, 1H, NH), 7.35 (d, 3H, J = 8.8 Hz, Ar–H), 7.85 (d, 2H, J = 8.0 Hz, Ar–H); 13C-NMR (100 MHz, CDCl3, δ ppm): 11.6, 13.7, 21.9, 39.8, 53.0, 107.7, 109.2, 111.0, 128.9, 130.0, 131.6, 140.6, 142.7, 143.1, 146.1, 146.7, 148.3, 152.0, 194.4; ESI–MS m/z: 421 [M + H]+; Analytical calculated formulae C21H20N6O2S: C, 59.98; H, 4.79; N, 19.99; S, 7.63; Found: C, 59.94; H, 4.7; N, 19.94; S, 7.68.
( ±)-(3-(3,5-Dimethyl-1H-pyrazol-1-yl)-6-(thiophen-2-yl)-6,7-dihydro-5H-[1,2,4]triazolo[3,4-b][1,3,4] thiadiazin-7-yl)(4-nitrophenyl)methanone (5s)
Golden color solid; yield 89%; m.p.: 204–206○C; IR (KBr, ʋmax/cm−1): 3281(NH), 1696 (C=O); 1H-NMR (400 MHz, CDCl3 + DMSO-d6, δ ppm): 2.26 (s, 3H, CH3), 2.27 (s, 3H, CH3), 5.47 (t, 1H, J = 3.6 Hz, CH), 5.88 (d, 1H, J = 3.2 Hz, CH), 6.10 (s, 1H, CH of pyrazole ring), 6.97 (t, 1H, J = 4.4 Hz, Ar–H), 7.17 (d, 1H, J = 4.4 Hz, Ar–H), 7.31 (d, 1H, J = 4.8 Hz, Ar–H), 7.35 (s, 1H, NH), 8.37 (s, 4H, Ar–H); 13C-NMR (100 MHz, CDCl3 + DMSO-d6, δ ppm): 11.4, 13.8, 42.9, 53.4, 107.5, 124.1, 126.3, 126.5, 127.4, 129.3, 130.8, 139.9, 142.9, 146.9, 149.6, 150.7, 151.3, 194.5; ESI–MS m/z: 468 [M + H]+; Analytical calculated formulae C20H17N7O3S: C, 51.38; H, 3.67; N, 20.97; S, 13.72; Found: C, 51.34; H, 3.62; N, 20.94; S, 13.76.
( ±)-(3-(3,5-Dimethyl-1H-pyrazol-1-yl)-6-(furan-2-yl)-6,7-dihydro-5H-[1,2,4]triazolo[3,4-b][1,3,4] thiadiazin-7-yl)(4-nitrophenyl)methanone (5t)
White solid; yield 92%; m.p.: 201–203○C; IR (KBr, ʋmax/cm−1): 3278 (NH), 1698 (C = O); 1H-NMR (400 MHz, CDCl3, δ ppm): 2.25 (s, 3H, CH3), 2.27 (s, 3H, CH3), 5.28–5.32 (m, 1H, CH), 5.78 (d, 1H, J = 4.0 Hz, CH), 6.08 (s, 1H, CH of pyrazole ring), 6.45 (s, 1H, NH), 7.14 (d, 1H, J = 4.0 Hz, Ar–H), 7.48 (d, 1H, J = 4.0 Hz, Ar–H), 7.85 (t, 1H, J = 8.4 Hz, Ar–H), 8.29 (d, 2H J = 8.4 Hz, Ar–H), 8.33 (d, 2H, J = 7.2 Hz, Ar–H); 13C-NMR (100 MHz, CDCl3, δ ppm): 11.2, 13.8, 49.8, 52.5, 107.5, 109.2, 111.0, 124.1, 124.3, 130.4, 130.6, 142.9, 143.0, 148.1, 149.1, 150.7 151.3, 194.0; ESI–MS m/z: 452 [M + H]+; Analytical calculated formulae C20H17N7O4S: C, 53.21; H, 3.80; N, 21.72; S, 7.10; Found: C, 53.25; H, 3.85; N, 21.7; S, 7.15.
X-ray crystallography
The diffraction data was collected on Bruker APEX2 single crystal X-ray diffractometere quipped with a CCD area detector system, graphite mono chromator and a Mo-Kα fine focus sealed tube (λ = 0.71073 Å). Bruker SAINT PLUS was used for data reduction, SHELXT-2014 [49] was used for structure solution and SHELXL-2018 [50] was used for full-matrix least-squares refinement. Mercury 3.3 [51] was used for molecular graphics. All non-hydrogen atoms were refined using anisotropic thermal parameters. All hydrogen atoms bound to carbons were positioned geometrically and refined using a riding model. Important crystallographic data and table for bond distances and bond angles were provided in supporting information.
Supplementary Information
Below is the link to the electronic supplementary material.
The 1H-NMR, 13C-NMR, and ESI–MS spectrum data are provided in supporting information. (dOCX 2540 kb)
Acknowledgements
We are thankful to the Head, Department of Chemistry and Director, National Institute of Technology, Warangal, Telangana, for providing infrastructure facilities and one of the authors P.C. Jilloju is thankful to MHRD government of India, for providing research fellowship.
Footnotes
Publisher's Note
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References
- 1.Wan J-P, Cao S, Liu Y. Base-promoted synthesis of N -substituted 1,2,3-triazoles via enaminone-azide cycloaddition involving regitz diazo transfer. Org Lett. 2016;18:6034–6037. doi: 10.1021/acs.orglett.6b02975. [DOI] [PubMed] [Google Scholar]
- 2.Wang X-Y, Zhong Y-F, Mo Z-Y, et al. Synthesis of seleno oxindoles via electrochemical cyclization of N -arylacrylamides with diorganyl diselenides. Adv Synth Catal. 2021;363:208–214. doi: 10.1002/adsc.202001192. [DOI] [Google Scholar]
- 3.Zhong P-F, Lin H-M, Wang L-W, et al. Electrochemically enabled synthesis of sulfide imidazopyridines via a radical cyclization cascade. Green Chem. 2020;22:6334–6339. doi: 10.1039/D0GC02125C. [DOI] [Google Scholar]
- 4.Guo Y, Wang G, Wei L, Wan J-P. Domino C-H sulfonylation and pyrazole annulation for fully substituted pyrazole synthesis in water using hydrophilic enaminones. J Org Chem. 2019;84:2984–2990. doi: 10.1021/acs.joc.8b02897. [DOI] [PubMed] [Google Scholar]
- 5.Wang M-R, Deng L, Liu G-C, et al. Porous organic polymer-derived nanopalladium catalysts for chemoselective synthesis of antitumor benzofuro[2,3- b ]pyrazine from 2-bromophenol and isonitriles. Org Lett. 2019;21:4929–4932. doi: 10.1021/acs.orglett.9b01230. [DOI] [PubMed] [Google Scholar]
- 6.Wan J-P, Jing Y, Hu C, Sheng S. Metal-free synthesis of fully substituted pyridines via ring construction based on the domino reactions of enaminones and aldehydes. J Org Chem. 2016;81:6826–6831. doi: 10.1021/acs.joc.6b01149. [DOI] [PubMed] [Google Scholar]
- 7.Tong W, Li W-H, He Y, et al. Palladium-metalated porous organic polymers as recyclable catalysts for the chemioselective synthesis of thiazoles from thiobenzamides and isonitriles. Org Lett. 2018;20:2494–2498. doi: 10.1021/acs.orglett.8b00886. [DOI] [PubMed] [Google Scholar]
- 8.Kaur P, Chawla A. 1,2,4-Triazole: a review of pharmacological activities. Int Res J Pharm. 2017;8:10–29. doi: 10.7897/2230-8407.087112. [DOI] [Google Scholar]
- 9.Bayrak H, Demirbas A, Demirbas N, Karaoglu SA. Synthesis of some new 1,2,4-triazoles starting from isonicotinic acid hydrazide and evaluation of their antimicrobial activities. Eur J Med Chem. 2009;44:4362–4366. doi: 10.1016/j.ejmech.2009.05.022. [DOI] [PubMed] [Google Scholar]
- 10.Burman WJ. Rip van winkle wakes up: Development of tuberculosis treatment in the 21st century. Clin Infect Dis. 2010;50:165–172. doi: 10.1086/651487. [DOI] [PubMed] [Google Scholar]
- 11.Abdel-Aal MT, El-Sayed WA, El-Kosy SM, El-Ashry ESH. Synthesis and antiviral evaluation of novel 5-(N-arylaminomethyl-1,3,4- oxadiazol-2-yl)hydrazines and their sugars, 1,2,4-triazoles, tetrazoles and pyrazolyl derivatives. Arch Pharm (Weinheim) 2008;341:307–313. doi: 10.1002/ardp.200700154. [DOI] [PubMed] [Google Scholar]
- 12.Benci K, Suhina T, Mandić L, et al. Novel 1,2,4-triazole and purine acyclic cyclopropane nucleoside analogues: synthesis, antiviral and cytostatic activity evaluations. Antivir Chem Chemother. 2011;21:221–230. doi: 10.3851/IMP1762. [DOI] [PubMed] [Google Scholar]
- 13.Rezaei Z, Khabnadideh S, Pakshir K, et al. Design, synthesis, and antifungal activity of triazole and benzotriazole derivatives. Eur J Med Chem. 2009 doi: 10.1016/j.ejmech.2008.07.012. [DOI] [PubMed] [Google Scholar]
- 14.Andrews B, Ahmed M. Synthesis and characterization of pyrimidine bearing 1,2,4-triazole derivatives and their potential antifungal action. Int J ChemTech Res. 2014;6:1013–1021. [Google Scholar]
- 15.Mathew V, Keshavayya J, Vaidya VP. Heterocyclic system containing bridgehead nitrogen atom: synthesis and pharmacological activities of some substituted 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazoles. Eur J Med Chem. 2006;41:1048–1058. doi: 10.1016/j.ejmech.2006.03.018. [DOI] [PubMed] [Google Scholar]
- 16.Jiang B, Huang X, Yao H, et al. Discovery of potential anti-inflammatory drugs: Diaryl-1,2,4-triazoles bearing N-hydroxyurea moiety as dual inhibitors of cyclooxygenase-2 and 5-lipoxygenase. Org Biomol Chem. 2014;12:2114–2127. doi: 10.1039/c3ob41936c. [DOI] [PubMed] [Google Scholar]
- 17.Abuo-Rahma GEDAA, Abdel-Aziz M, Beshr EAM, Ali TFS. 1,2,4-Triazole/oxime hybrids as new strategy for nitric oxide donors: synthesis, anti-inflammatory, ulceroginicity and antiproliferative activities. Eur J Med Chem. 2014;71:185–198. doi: 10.1016/j.ejmech.2013.11.006. [DOI] [PubMed] [Google Scholar]
- 18.Shivarama Holla B, Veerendra B, Shivananda M, Poojary B. Synthesis characterization and anticancer activity studies on some Mannich bases derived from 1,2,4-triazoles. Eur J Med Chem. 2003;38:759–767. doi: 10.1016/S0223-5234(03)00128-4. [DOI] [PubMed] [Google Scholar]
- 19.Plech T, Luszczki JJ, Wujec M, et al. Synthesis, characterization and preliminary anticonvulsant evaluation of some 4-alkyl-1,2,4-triazoles. Eur J Med Chem. 2013;60:208–215. doi: 10.1016/j.ejmech.2012.11.026. [DOI] [PubMed] [Google Scholar]
- 20.Cetin A, Geçibesler IH. Evaluation as antioxidant agents of 1,2,4-triazole derivatives: effects of essential functional groups. J Appl Pharm Sci. 2015;5:120–126. doi: 10.7324/JAPS.2015.50620. [DOI] [Google Scholar]
- 21.Ongini E, Monopoli A, Cacciari B, Giovanni Baraldi P. Selective adenosine A2A receptor antagonists. Farm. 2001;56:87–90. doi: 10.1016/S0014-827X(01)01024-2. [DOI] [PubMed] [Google Scholar]
- 22.Messore A, Corona A, Madia VN, et al. Pyrrolyl pyrazoles as non-diketo acid inhibitors of the HIV-1 ribonuclease H function of reverse transcriptase. ACS Med Chem Lett. 2020;11:798–805. doi: 10.1021/acsmedchemlett.9b00617. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Kim J, Lee D, Park C, et al. Discovery of phenylaminopyridine derivatives as novel HIV-1 non-nucleoside reverse transcriptase inhibitors. ACS Med Chem Lett. 2012;3:678–682. doi: 10.1021/ml300146q. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Jiang B, Fan W, Sun MY, et al. Domino reaction of arylglyoxals with pyrazol-5-amines: selective access to pyrazolo-fused 1,7-naphthyridines, 1,3-diazocanes, and pyrroles. J Org Chem. 2014;79:5258–5268. doi: 10.1021/jo500823z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Renuka N, Ajay Kumar K. Synthesis and biological evaluation of novel formyl-pyrazoles bearing coumarin moiety as potent antimicrobial and antioxidant agents. Bioorganic Med Chem Lett. 2013;23:6406–6409. doi: 10.1016/j.bmcl.2013.09.053. [DOI] [PubMed] [Google Scholar]
- 26.Tewari AK, Srivastava P, Singh VP, et al. Novel anti-inflammatory agents based on pyrazole based dimeric compounds; design, synthesis, docking and in vivo activity. Chem Pharm Bull (Tokyo) 2010;58:634–638. doi: 10.1248/cpb.58.634. [DOI] [PubMed] [Google Scholar]
- 27.Vijesh AM, Isloor AM, Shetty P, et al. New pyrazole derivatives containing 1,2,4-triazoles and benzoxazoles as potent antimicrobial and analgesic agents. Eur J Med Chem. 2013;62:410–415. doi: 10.1016/j.ejmech.2012.12.057. [DOI] [PubMed] [Google Scholar]
- 28.Poce G, Consalvi S, Venditti G, et al. Novel pyrazole-containing compounds active against mycobacterium tuberculosis. ACS Med Chem Lett. 2019;10:1423–1429. doi: 10.1021/acsmedchemlett.9b00204. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Park HJ, Lee K, Park SJ, et al. Identification of antitumor activity of pyrazole oxime ethers. Bioorganic Med Chem Lett. 2005;15:3307–3312. doi: 10.1016/j.bmcl.2005.03.082. [DOI] [PubMed] [Google Scholar]
- 30.Sener A, Kasimogullari R, Sener MK, Genc H. Studies on reactions of cyclic oxalyl compounds with hydrazines or hydrazones. 2. Synthesis and reactions of 4-benzoyl-1-(4-nitrophenyl)-5-phenyl- 1H-pyrazole-3-carboxylic acid. Chem Heterocycl Compd. 2004;40:1039–1046. doi: 10.1023/B:COHC.0000046695.00178.79. [DOI] [Google Scholar]
- 31.Menozzi G, Mosti L, Fossa P, et al. ω-Dialkylaminoalkyl ethers of phenyl-(5-substituted 1-phenyl-1 H -pyrazol-4-yl)methanols with analgesic and anti-inflammatory activity. J Heterocycl Chem. 1997;34:963–968. doi: 10.1002/jhet.5570340339. [DOI] [Google Scholar]
- 32.Magedov IV, Manpadi M, Van Slambrouck S, et al. Discovery and investigation of antiproliferative and apoptosis-inducing properties of new heterocyclic podophyllotoxin analogues accessible by a one-step multicomponent synthesis. J Med Chem. 2007;50:5183–5192. doi: 10.1021/jm070528f. [DOI] [PubMed] [Google Scholar]
- 33.Mowbray CE, Braillard S, Speed W, et al. Novel amino-pyrazole ureas with potent in vitro and in vivo antileishmanial activity. J Med Chem. 2015;58:9615–9624. doi: 10.1021/acs.jmedchem.5b01456. [DOI] [PubMed] [Google Scholar]
- 34.Zhang B, Li Y-H, Liu Y, et al. Design, synthesis and biological evaluation of novel 1,2,4-triazolo [3,4-b][1,3,4] thiadiazines bearing furan and thiophene nucleus. Eur J Med Chem. 2015;103:335–342. doi: 10.1016/j.ejmech.2015.08.053. [DOI] [PubMed] [Google Scholar]
- 35.Shah TA, Ahmad Z, Mir NA, et al. One step synthesis of highly functionalized thiazolo[3{,}2-b][1{,}2{,}4]triazole{,} triazolo[1{,}5-a]pyrimidine and triazolo[3{,}4-b][1{,}3{,}4]thiadiazine. RSC Adv. 2015;5:107931–107937. doi: 10.1039/C5RA21270G. [DOI] [Google Scholar]
- 36.Khan I, Ibrar A, Abbas N. Triazolothiadiazoles and triazolothiadiazines – biologically attractive scaffolds. Eur J Med Chem. 2013;63:854–868. doi: 10.1016/j.ejmech.2013.01.060. [DOI] [PubMed] [Google Scholar]
- 37.Sumangala V, Poojary B, Chidananda N, et al. Facile synthesis, cytotoxic and antimicrobial activity studies of a new group of 6-aryl-3-[4-(methylsulfonyl)benzyl]-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazines. Eur J Med Chem. 2012;54:59–64. doi: 10.1016/j.ejmech.2012.04.024. [DOI] [PubMed] [Google Scholar]
- 38.Khan I, Zaib S, Ibrar A, et al. Synthesis, crystal structure and biological evaluation of some novel 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazoles and 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazines. Eur J Med Chem. 2014;78:167–177. doi: 10.1016/j.ejmech.2014.03.046. [DOI] [PubMed] [Google Scholar]
- 39.Pundeer R, Kiran V, Prakash R, et al. α, α-Dibromoacetophenones mediated synthesis of some new 7H–7-alkoxy-3-alkyl/phenyl-6-aryl-s-triazolo[3,4-b][1,3,4]thiadiazines and their antimicrobial evaluation. Med Chem Res. 2012;21:4043–4052. doi: 10.1007/s00044-011-9945-1. [DOI] [Google Scholar]
- 40.Saha A, Payra S, Banerjee S. One-pot multicomponent synthesis of highly functionalized bio-active pyrano[2,3-c]pyrazole and benzylpyrazolyl coumarin derivatives using ZrO 2 nanoparticles as a reusable catalyst. Green Chem. 2015;17:2859–2866. doi: 10.1039/C4GC02420F. [DOI] [Google Scholar]
- 41.Bhunia A, Porwal D, Gonnade RG, Biju AT. Multicomponent reactions involving arynes, quinolines, and aldehydes. Org Lett. 2013;15:4620–4623. doi: 10.1021/ol4023134. [DOI] [PubMed] [Google Scholar]
- 42.Cioc RC, Ruijter E, Orru RVA. Multicomponent reactions: advanced tools for sustainable organic synthesis. Green Chem. 2014;16:2958–2975. doi: 10.1039/C4GC00013G. [DOI] [Google Scholar]
- 43.Jilloju PC, Shyam P, Sanjeev A, Vedula RR. Four-component, one–pot synthesis of (E)-N-benzylidene-3-(benzylthio)-5-(3,5-dimethyl-1H-pyrazol-1-yl)-4H-1,2,4-triazol-4-amines and their DNA binding and molecular docking studies. J Mol Struct. 2021;1225:129140. doi: 10.1016/j.molstruc.2020.129140. [DOI] [Google Scholar]
- 44.Mamidala S, Peddi SR, Aravilli RK, et al. Microwave irradiated one pot, three component synthesis of a new series of hybrid coumarin based thiazoles: Antibacterial evaluation and molecular docking studies. J Mol Struct. 2021 doi: 10.1016/j.molstruc.2020.129114. [DOI] [Google Scholar]
- 45.Sujatha K, Vedula RR. Multicomponent Efficient synthesis of new [1,2,4]Triazolo[3,4]thiadiazines. J Heterocycl Chem. 2019;56:832–838. doi: 10.1002/jhet.3458. [DOI] [Google Scholar]
- 46.Jilloju PC, Vedula RR. A facile one-pot three-component synthesis of benzylideneamino-3,5-dimethyl-1H-pyrazoles. Synth Commun. 2018;48:1739–1746. doi: 10.1080/00397911.2018.1458242. [DOI] [Google Scholar]
- 47.Div MC, College SC. 4-Amino-3-pyrazolo-l,2,4-triazoles as antimicrobial agents+ Arch Pharm. 1989;66:63–66. doi: 10.1002/ardp.19893220202. [DOI] [PubMed] [Google Scholar]
- 48.Al-Etaibi A, John E, Ibrahim MR, et al. Stereoselective synthesis of dihydrothiadiazinoazines and dihydrothiadiazinoazoles and their pyrolytic desulfurization ring contraction. Tetrahedron. 2011;67:6259–6274. doi: 10.1016/j.tet.2011.06.034. [DOI] [Google Scholar]
- 49.Sheldrick GM. SHELXT - Integrated space-group and crystal-structure determination. Acta Crystallogr Sect A Found Crystallogr. 2015;71:3–8. doi: 10.1107/S2053273314026370. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Sheldrick GM. Crystal structure refinement with SHELXL. Acta Crystallogr Sect C Struct Chem. 2015;71:3–8. doi: 10.1107/S2053229614024218. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51.Macrae CF, Bruno IJ, Chisholm JA, et al. Mercury CSD 2.0 - New features for the visualization and investigation of crystal structures. J Appl Crystallogr. 2008;41:466–470. doi: 10.1107/S0021889807067908. [DOI] [Google Scholar]
Associated Data
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Supplementary Materials
The 1H-NMR, 13C-NMR, and ESI–MS spectrum data are provided in supporting information. (dOCX 2540 kb)