Preparation of 3-Substituted Isoindolin-1-one, Cinnoline, and 1,2,4-[e]-Benzotriazine Derivatives.

Herein, we report a new approach to synthesize a series of 1,2,4-[e]-benzotriazine and cinnoline derivatives from 3-substituted isoindolin-1-one. All the reported products are obtained through an economical two-step synthetic procedure resulting in fair-to-high yields. Cinnolines (a) and 1,2,4-[e]-benzotriazines (b) result from an intramolecular cyclization of the corresponding 3-substituted isoindolin-1-ones, which, in turn, are prepared by an addition reaction from 2-cyanobenzaldehyde and 2-(2-nitrophenyl) acetonitrile (a) or 2-nitroaniline derivatives (b). A proposed mechanism for this transformation is presented.

Introduction

Synthetic heterocyclic chemistry has made notable progress in the last few decades.[1−4] Isoindolinones, cinnolines, and 1,2,4-benzotriazines represent important classes of nitrogen-containing compounds.[5] In fact, it is reported that seven of the top ten selling drugs in the world are nitrogen-containing heterocycles.[6] Consequently, these heterocyclic compounds have received considerable attention in organic chemistry ranging from their methods of preparation to studies of their physical, chemical, and biological properties.[1,2] The growing interest in these N-containing compounds is the result of their wide ranging biological activities such as antimalarial,[7,8] antibacterial,[9,10] antiviral, antifungal,[11] anthelmintic, and anticancer properties for application in pharmaceutical fields (Figure ).[12−14]

Figure 1

Cinnoline, 1,2,4-[e]-benzotriazine and isoindolinone drugs.

In addition, some analogues of these heterocycles have demonstrated electro-optical activities, and others have been used as dyes (Figure ).[15]

Figure 2

CinNapht dye.

Taking into consideration all these previous applications, 1,2,4-[e]-benzotriazine and cinnoline heterocycles have been synthesized through various multistep reactions over the past several years.[1] Given their importance, we have developed a simple synthetic method based on reactions and mechanisms reported by Sato et al. (Scheme )[16] and Angelin et al. (Scheme ),[17,18] where 2-cyanobenzaldehyde (1), 2-(2-nitrophenyl) acetonitrile (2; see Scheme ), or 2-nitroaniline substituents (7a–h; see Scheme ) are employed as starting materials.

Scheme 1

Sato et al.’s Synthesis of 3-N Substituted Isoindolin-1-ones

Scheme 2

Angelin et al.’s Mechanism-Based Synthesis of 3-Nitrosubstituted Isoindolinones

Scheme 3

Mechanism for the Synthesis of 2-(2-Nitrophenyl)-2-(3-oxoisoindolin-1-yl)acetonitrile (6)

Scheme 4

Sato Mechanism Applied to the Synthesis of 3-Aminoisoindolin-1-ones 10a–h

We succeeded in synthesizing a series of substituted isoindolin-1-ones as well as their corresponding novel cinnolines and 1,2,4-[e]-benzotriazines. In this paper, we present the synthesis of the latter compounds through a two-step reaction, which is economical and produces good yield.

Results and Discussion

The synthesis of novel 2-(2-nitrophenyl)-2-(3-oxoisoindolin-1-yl)acetonitrile (6) was accomplished through a nucleophilic addition reaction (1 + 3 → 4), followed by a cyclization (4 → 5) and subsequent rearrangement (5 → 6) process between 2-cyanobenzaldehyde (1) and 2-(2-nitrophenyl) acetonitrile (2). The mechanism for this one-pot process is illustrated in Scheme .

1H NMR, 13C NMR, and 13C NMR DEPT 135 spectra were consistent with the structure of 6. Similar to the work reported by Angelin et al., triethylamine was proved most desirable for the reaction.[18] It is important to abstract the proton at the α-position to the nitro group or between the two withdrawing groups as described in the literature.[17,18] In our case, Et3N abstracted α-H to the nitrile group and generated a nucleophilic specie in the medium. In fact, replacing Et3N with 5% KOH in methanol led to several undesired side products. In addition, the amount of solvent used, methanol in this reaction, was an important factor affecting the product yield; it should be minimized in order to precipitate isoindolin-1-one 6 as it forms. Formation of the isoinolin-1-one carbonyl group was shown by a peak at 1703 cm–1 in the IR spectra, compared to that of the 2-cyanobenzaldehyde carbonyl group at 1693 cm–1. This isoindolin-1-one (6) was isolated as a pure white powder, which was sensitive to light turning the material dark brown. This observation might be explained by the reaction of the nitro group oxygen with the benzylic proton of the cyano group. This reaction also applies to 2-nitrobenzaldehyde yielding 2-nitrosobenzoic acid.[19]

The synthesis of 3-aminoisoindolin-1-one derivatives 10a–h (Scheme ) has been achieved following the same procedure as described for product 6: specifically, a nucleophilic addition reaction between the aldehyde function of the 2-cyanobenzaldehyde (1) and the amine function of the 2-nitroaniline derivatives (7a–h), followed by cyclization and rearrangement.

In keeping with the mechanism reported by the Sato et al. group in 1984,[16] the aniline nitrogen lone pair attacks the carbonyl, and the resulting alkoxide anion then attacks the cyano group to form the cyclic intermediate products 9a–h. A simple subsequent rearrangement occurs to give the lactam isoindolin-1-ones 10a–h.

In contrast to the reaction described in Scheme , nitrogen base; triethylamine Et3N in our case blocked the reaction and stopped the progress of the isoindolinone formation. Instead, a few drops of the strong base methanolic KOH (5%) initiated the formation of the products 10a–h. Starting from a 1:1.2 mmol equivalent of nitroaniline derivatives, 0.4 mL of 2-cyanobenzaldehyde was sufficient for the isolation of the product. Yet, increasing the volume of the base led to some undesired side reactions that decreased the yield of our isoindolinone intermediates. In addition, the solvent nature was found to have an effect on product formation: when using methanol, ethyl acetate, chloroform, and even dimethylformamide, the yields were very low. Fortunately, adding a small amount of dichloromethane (1 mL) resulted in maximum isolation of the desired 3-substituted isoindolin-1-ones 10a–h as yellow pastes, which were subsequently filtrated and washed with cold methanol. The isolated % yield of product 10c using various solvents are shown in Table .

Table 1

Isolated % Yields of 10c in Different Solvents

solvent	DCM	EtOAc	MeOH	CHCl3	DMF
% yield of 10c	76	39	36	42	65

Finally, upon heating in 5% methanolic KOH, compound 6 gave the corresponding cinnolines 14 and 15, and compounds 10a–h produced the 1,2,4-[e]-benzotriazines 16a–h and 17a–h. The postulated mechanisms for the formation of 14–17 are described in Schemes and 6. All structures were supported by full spectral data characterization (1H NMR, 13C NMR, 13C NMR DEPT 135, IR, and HR-MS) as well as melting points.

Scheme 5

Synthesis of Cinnolines 14 and 15 through the Formation of Isoindolinone 6

Scheme 6

Synthesis of 1,2,4-[e]-Benzotriazines 16a–h and 17a–h from 3-Substituted Isoindolinones 10a–h

In addition, the structure of methyl 2-(7-methoxybenzo[e][1,2,4] triazin-3-yl)benzoate (16d) was also established by X-ray crystallography (Figure ).

Figure 3

X-ray crystallography of product 16d.

While esters (14 and 16a–h) were the anticipated products from intramolecular cyclization of the isoindolin-1-ones, thin layer chromatography showed the presence of two spots and, indeed, two products were obtained—the esters (14 and 16a–h) as well as the much more polar hydrolyzed acids (15 and 17a–h). In fact, heating the reaction for 30 min caused the ester product to rapidly and completely hydrolyze the carboxylate salt. This is a direct consequence of the increased reaction temperature (∼65 °C) and 1 h heating at 60–65 °C. The formation of 15 from 14 is evident from the isolated yields of 14 and 15 as presented in Table .

Table 2

Isolated % Yields of the Cinnoline Ester 14 and Cinnoline Acid 15 Products Upon Heating

heating time	% yield of 14	% yield of 15	combined % yield of 14 and 15
15 min	82	15	97
30 min	60	34	94
1 h	17	76	93

Additionally, in the course of this investigation, a serendipitous reaction was found to occur with isoindolinone 10g. It formed benzotriazines 16g and 17g by electrophilic aromatic substitution of the chloro group para to the nitro moiety. Indeed, the 1H and 13C NMR data were incompatible with the expected dichloro structures. Theoretically, the dichloro products should show three methoxy protons for the ester at ∼4 ppm in 1H NMR as well as a OCH3 carbon at ∼50 ppm in the 13C NMR. Experimentally, six methoxy protons appeared as two singlets at 4.13 and 4.03 ppm and two OCH3 carbons at 57.25 and 57.23 ppm, in addition to the other expected peaks. This result can be explained by chloride displacement by methoxide upon heating of 10g, where CH3O– displaces the chlorine at position 6, para to the nitro group (Scheme ).

Scheme 7

Synthesis of Methyl 2-(7-Chloro-6-methoxybenzo[e][1,2,4]triazin-3-yl)benzoate 16g and 2-(7-Chloro-6-methoxybenzo[e][1,2,4]triazin-3-yl)benzoic Acid 17g

Conclusions

A total of 27 compounds were successfully synthesized, identified, and characterized by melting points, 1H NMR, 13C NMR, 13C NMR DEPT 135, FT-IR, and HR-MS spectroscopy. The synthesis was accomplished through new, concise, efficient, and low-cost reactions, resulting in fair-to-high yields of the products.

Experimental Section

Melting points were determined using a DigiMelt digital melting point apparatus and were uncorrected. 1H MNR, 13C NMR, and Dept 135 spectra were determined in CDCl3 or DMSO-d6 using a Bruker AM 500 NMR spectrometer. Chemical shifts were recorded in ppm (δ). Infrared spectra were collected using a Thermo Scientific iD3 ATR for Nicolet iS5 FT-IR spectrometer in cm–1. High-resolution mass spectra (HR-MS) were recorded using a SCIEX X500R HPLC/QTOF mass spectrometer. Thin layer chromatography (TLC) was performed on TLC silica gel 60 F254. Required starting materials were commercially available.

2-(2-Nitrophenyl)-2-(3-oxoisoindolin-1-yl)acetonitrile (6)

o-Cyanobenzaldehyde (0.32 g; 2.50 mmol) and 2-(2-nitrophenyl)acetonitrile (0.34 g; 2.08 mmol) were dissolved in 3 mL of MeOH. A volume of 0.5 mL of Et3N was added while stirring the mixture at room temperature. After 2 min, a white precipitate appeared. The product was collected by suction filtration and was washed with cold ethanol (0.48 g; 79%). Melting point: 203 °C; 1H NMR (500 MHz, DMSO-d6): δ 8.25 (d, J = 8.0, 1.0 Hz, 1H), 7.89 (dd, J = 7.5, 1.5 Hz, 1H), 7.85 (d, J = 7.5 Hz, 1H), 7.72–7.75 (m, 3H), 7.60–7.67 (m, 2H), 7.48 (s, 1H), 5.51 (d, J = 3 Hz, 1H), 5.22 (d, J = 2.5 Hz, 1H); 13C NMR (126 MHz, DMSO-d6): δ 171.11, 147.38, 143.27, 135.03, 133.07, 132.09, 131.42, 130.58, 129.94, 127.34, 126.39, 124.33, 122.89, 116.04, 58.38, 40.23 ppm; DEPT 135 (126 MHz, DMSO-d6): δ 135.03, 133.07, 131.42, 130.58, 129.94, 126.39, 124.33, 122.89, 58.38, 40.24; FTIR (cm–1): 2361 (m), 2343 (w), 1703 (s), 1615 (w), 1532 (s), 1470 (m), 1348 (s), 1306 (w), 1138 (m), 858 (m), 758 (m), 721 (s), 703 (s); m/z: calcd for C16H11N3O3 [M + H]+, 294.08732; found, 294.0874, [M + Na]+, calcd 316.06926; found, 316.0693, [M + K]+, calcd 332.0432; found, 332.0418.

General Procedure A

Derivatives of 3-((nitrophenyl)amino)isoindolin-1-one were prepared from 2-cyanobenzaldehyde (0.32 g; 2.50 mmol) and 2-nitroaniline derivatives (1 mmol) dissolved in 1 mL of DCM. The mixture was warmed to ensure total dissolution of all the starting materials for 1 min. The reaction mixture was then cooled to room temperature, and 0.4 mL of 5% KOH in MeOH was added. The solution color turned red, and heat was released just before a yellow paste formed. The product was collected by suction filtration and washed with water and cold methanol.

3-((Nitrophenyl)amino)isoindolin-1-one (10a)

This product was synthesized according to general procedure A as a yellow solid (0.21 g; 79%). Melting point: 235 °C; 1H NMR (500 MHz, DMSO-d6): δ 9.29 (s, 1H), 8.20 (d, J = 8.5 Hz, 1H), 8.12 (dd, J = 8.5, 1.5 Hz, 1H), 7.76 (d, J = 7.5 Hz, 1H), 7.69 (dt, J = 7.0, 1.5 Hz, 1H), 7.65–7.67 (m, 1H), 7.62 (dt, J = 7.0, 1.5 Hz, 1H), 7.56–7.60 (m, 1H), 7.21 (d, J = 8.5 Hz, 1H), 6.85–6.88 (m, 1H), 6.51 (d, J = 8 Hz, 1H); 13C NMR (126 MHz, DMSO-d6): δ 169.34, 145.03, 143.66, 136.91, 133.16, 133.05, 132.81, 130.19, 126.76, 123.95, 123.53, 117.82, 116.12, 64.35 ppm; 13C NMR DEPT 135 (126 MHz, DMSO-d6): δ 136.91, 133.05, 130.20, 126.76, 123.95, 123.53, 117.82, 116.13, 64.35; FTIR (cm–1): 1714 (s), 1619 (m), 1577 (m), 1498 (m), 1470 (w), 1446 (m), 1409 (w), 1346 (m), 1262 (m), 1228 (m), 1138 (w), 1122 (m), 1069 (w), 869 (w), 738 (s), 696 (w); m/z: calcd for C14H11N3O3 [M + H]+, 270.08732; found, 270.1003, [M + Na]+, calcd 292.06926; found, 292.0696, [M + K]+, calcd 308.0432; found, 308.0528.

3-((4-Methyl-2-nitrophenyl)amino)isoindolin-1-one (10b)

This product was synthesized according to the general procedure A as a yellow solid (0.20 g; 70%). Melting point 209 °C; 1H NMR (500 MHz, DMSO-d6): δ 9.26 (s, 1H), 8.08 (d, J = 8.0 Hz, 1H), 7.93 (d, J = 1.0 Hz, 1H), 7.75 (d, J = 7.0 Hz, 1H), 7.68 (dt, J = 7.5, 1.0 Hz, 1H), 7.64 (d, J = 7.0 Hz, 1H), 7.61 (dt, J = 7.5, 1.0 Hz, 1H), 7.42 (dd, J = 9.0, 2.0 Hz 1H), 7.13 (d, J = 8.5 Hz, 1H), 6.48 (d, J = 8.0 Hz, 1H), 2.26 (s, 3H); 13C NMR (126 MHz, DMSO-d6): δ 169.32, 145.14, 141.79, 138.15, 133.01, 132.88, 132.81, 130.14, 127.12, 125.84, 123.90, 123.50, 116.23, 64.49, 19.91 ppm; DEPT 135 (126 MHz, DMSO-d6): δ 138.16, 133.01, 130.14, 127.12, 125.84, 123.90, 123.50, 116.23, 64.49, 19.91; FTIR (cm–1): 1710 (s), 1633 (w), 1567 (w), 1524 (m), 1470 (w), 1443 (w), 1409 (w), 1348 (m), 1316 (w), 1273 (m), 1237 (w), 1206 (m), 1156 (w), 1124 (w), 1063 (w), 924 (w), 792 (w), 762 (m), 741 (m), 706 (m); m/z: calcd for C15H13N3O3 [M + H]+, 284.10297, found 284.1037, [M + Na]+, calcd 306.08491; found, 306.0855, [M + K]+, calcd 322.05885; found, 322.0588.

3-((4.5-Dimethyl-2-nitrophenyl)amino)isoindolin-1-one (10c)

This product was synthesized according to general procedure A as a yellow solid (0.23 g; 77%). Melting point: 257 °C; 1H NMR (500 MHz, DMSO-d6): δ 9.31 (s, 1H), 8.06 (d, J = 8.5 Hz, 1H), 7.91 (s, 1H), 7.75 (d, J = 7.5 Hz, 1H), 7.70 (dt, J = 7.5, 1.0 Hz, 1H), 7.66 (d, J = 7.0 Hz, 1H), 7.62 (dt, J = 7.5, 1.0 Hz, 1H), 7.15 (s, 1H), 6.49 (d, J = 8.0 Hz, 1H), 2.26 (s, 3H), 2.20 (s, 3H); 13C NMR (126 MHz, DMSO-d6): δ 169.34, 147.88, 145.14, 142.21, 133.07, 132.76, 130.86, 130.21, 126.75, 126.06, 123.93, 123.48, 116.54, 64.27, 20.65, 18.56 ppm; DEPT 135 (126 MHz, DMSO-d6): δ 133.07, 130.21, 126.06, 123.93, 123.93, 123.48, 116.54, 64.27, 20.65, 18.56; FTIR (cm–1): 1707 (s), 1632 (w), 1569 (w), 1508 (m), 1471 (w), 1446 (w), 1409 (w), 1330 (w), 1279 (m), 1248 (m), 1210 (w), 1119 (m), 1054 (w), 846 (w), 733 (m); m/z: calcd for C16H15N3O3 [M + H]+, 298.11862; found, 298.1318, [M + Na]+, calcd 320.10056; found, 320.1008, [M + K]+, calcd 336.0745; found, 336.0748.

3-((4-Methoxy-2-nitrophenyl)amino)isoindolin-1-one (10d)

This product was synthesized according to general procedure A as an orange solid (0.25 g; 83%). Melting point: 208 °C; 1H NMR (500 MHz, DMSO-d6): δ 9.24 (s, 1H), 8.03 (d, J = 8.5 Hz, 1H), 7.74 (d, J = 7.5 Hz, 1H), 7.68 (t, J = 7.0 Hz, 1H), 7.64 (d, J = 7.0 Hz, 1H), 7.61 (t, J = 7.5 Hz, 1H), 7.57 (d, J = 3 Hz, 1H), 7.30 (dd, J = 9.5, 3.0 Hz, 1H), 7.18 (d, J = 9.5 Hz, 1H), 6.47 (d, J = 8.5 Hz, 1H), 3.77 (s, 3H); 13C NMR (126 MHz, DMSO-d6): δ 169.27, 150.88, 145.19, 138.94, 133.01, 132.82, 132.73, 130.15, 126.66, 123.91, 123.51, 117.86, 107.76, 64.74, 56.21 ppm; 13C NMR DEPT 135 (126 MHz, DMSO-d6): δ 133.01, 130.15, 126.66, 123.91, 123.51, 117.86, 107.76, 64.74, 56.21; FTIR (cm–1): 1707 (s), 1576 (w), 1526 (m), 1509 (w) 1416 (w), 1343 (w), 1237 (m), 1206 (w), 1058 (m), 1037 (m), 741 (m); m/z: calcd for C15H13N3O4 [M + H]+, 300.09788; found, 300.0993, [M + Na]+, calcd 322.07983; found, 322.0805, [M + K]+, calcd 338.05376; found, 338.0540.

3-((5-Methoxy-2-nitrophenyl)amino)isoindolin-1-one (10e)

This product was synthesized according to general procedure A as a pale yellow solid (0.27 g; 90%). Melting point: 257 °C; 1H NMR (500 MHz, DMSO-d6): δ 9.37 (s, 1H), 8.50 (d, J = 8.0 Hz, 1H), 8.09 (d, J = 9.5 Hz, 1H), 7.77 (d, J = 7.5 Hz, 1H), 7.70 (dd, J = 6.5, 1.0 Hz, 2H), 7.63 (dt, J = 7.0, 1.5 Hz, 1H), 6.57 (d, J = 8.0 Hz, 2H), 6.45 (dd, J = 9.5, 2.5 Hz, 1H), 3.83 (s, 3H); 13C NMR (126 MHz, DMSO-d6): δ 169.35, 165.94, 146.29, 144.85, 133.16, 132.77, 130.28, 129.10, 127.09, 123.98, 123.55, 107.24, 97.70, 64.17, 56.46 ppm; 13C NMR DEPT 135 (126 MHz, DMSO-d6): δ 133.16, 130.28, 129.10, 123.98, 123.55, 107.24, 97.70, 64.18, 56.46; FTIR (cm–1): 1709 (s), 1615 (m), 1584 (m), 1499 (m), 1421 (m), 1365 (w), 1313 (w), 1236 (s), 1122 (m), 1088 (w), 1071 (m), 845 (s), 785 (m), 735 (m); m/z: calcd for C15H13N3O4 [M + H]+, 300.09788; found, 300.1072, [M + Na]+, calcd 322.07983; found, 322.0800, [M + K]+, calcd 338.05376; found, 338.0541.

3-((4-Chloro-2-nitrophenyl)amino)isoindolin-1-one (10f)

This product was synthesized according to general procedure A as a yellow solid (0.24 g; 79%). Melting point: 236 °C; 1H NMR (500 MHz, DMSO-d6): δ 9.26 (s, 1H), 8.20 (d, J = 8.0 Hz, 1H), 8.12 (d, J = 2.5 Hz, 1H), 7.75 (d, J = 7.5 Hz, 1H), 7.68 (dt, J = 7.5, 1.0 Hz, 1H), 7.65 (d, J = 2.5 Hz, 1H), 7.63 (t, J = 2.5 Hz, 1H), 7.61 (dd, J = 7.0, 1.0 Hz, 1H), 7.23 (d, J = 9.5 Hz, 1H), 6.51 (d, J = 8 Hz, 1H); 13C NMR (126 MHz, DMSO-d6): δ 169.29, 144.80, 142.53, 136.46, 133.33, 133.04, 132.84, 130.22, 125.63, 123.96, 123.54, 120.96, 118.18, 64.46 ppm; DEPT 135 (126 MHz, DMSO-d6): δ 136.46, 133.04, 130.22, 125.63, 123.96, 123.54, 118.18, 64.46; FTIR (cm–1): 1708 (s), 1615 (w), 1564 (w), 1520 (m), 1501 (m), 1442 (w), 1409 (m), 1345 (m), 1298 (w), 1265 (s), 1210 (w), 1155 (m), 1123 (w), 1057 (w), 893 (m), 818 (m), 729 (m), 704 (m); m/z: calcd for C14H10ClN3O3 [M + H]+, 304.04835; found, 304.1496, [M + Na]+, calcd 326.03029; found, 326.0305, [M + K]+, calcd 342.00423; found, 342.0034.

3-((4,5-Dichloro-2-nitrophenyl)amino)isoindolin-1-one (10g)

This product was synthesized according to general procedure A as a yellow solid (0.30 g; 87%). Melting point: 257 °C; 1H NMR (500 MHz, DMSO-d6): δ 9.32 (s, 1H), 8.32 (s, 1H), 8.18 (d, J = 8.5 Hz, 1H), 7.75 (d, J = 7.5 Hz, 1H), 7.70 (dt, J = 7.5, 1.0 Hz, 1H), 7.66 (d, J = 7 Hz, 1H), 7.63 (dt, J = 7.5, 1.0 Hz, 1H), 7.57 (s, 1H), 6.56 (d, J = 8.5 Hz, 1H); 13C NMR (126 MHz, DMSO-d6): δ 169.32, 144.50, 142.82, 139.66, 133.06, 132.79, 132.33, 130.31, 127.79, 124.06, 123.50, 119.11, 117.65, 64.33 ppm; DEPT 135 (126 MHz, DMSO-d6): δ 133.09, 130.31, 127.79, 124.06, 123.50, 117.65, 64.33; FTIR (cm–1): 1713 (s), 1615 (m), 1553 (m), 1469 (s), 1331 (w), 1276 (m), 1260 (s), 1218 (m), 1072 (m), 756 (s), 633 (s); m/z: calcd for C14H9Cl2N3O3 [M + H]+, 338.00937; found, 338.0095, [M + Na]+, calcd 359.99132; found, 359.9914, [M + K]+, calcd 375.96525; found, 375.9636.

3-((2-Nitro-4-(trifluoromethyl)phenyl)amino)isoindolin-1-one (10h)

This product was synthesized according to general procedure A as a yellow solid (0.13 g; 39%). Melting point: 209 °C; 1H NMR (500 MHz, DMSO-d6): δ 9.28 (s, 1H), 8.50 (d, J = 8.5 Hz, 1H), 8.37 (d, J = 1.5 Hz, 1H), 7.88 (dd, J = 9.0, 2.0 Hz, 1H), 7.76 (d, J = 7.5 Hz, 1H), 7.69 (dt, J = 7.5, 1.0 Hz, H), 7.66 (d, J = 6.5 Hz, 1H), 7.63 (dt, J = 7.5, 1.5 Hz, 1H), 7.37 (d, J = 9.5 Hz, 1H), 6.59 (d, J = 8 Hz, 1H); 13C NMR (126 MHz, DMSO-d6): δ 169.35, 145.76, 144.55, 133.07, 132.84, 132.43, 130.28, 125.17, 124.47, 124.43, 124.00, 123.58, 117.59, 117.36, 64.32 ppm; DEPT 135 (126 MHz, DMSO-d6): δ 133.07, 132.43, 130.28, 124.47, 124.43, 124.00, 123.58, 117.36, 64.32; FTIR (cm–1): 1709 (s), 1635 (m), 1571 (w), 1534 (m), 1469 (w), 1446 (w), 1426 (w), 1335 (s), 1303 (w), 1271 (m), 1238 (w), 1211 (w), 1159 (m), 1111 (s), 1089 (w), 1064 (w), 914 (w), 763 (w), 744 (m), 715 (m); m/z: calcd for C15H10F3N3O3 [M + H]+, 338.0747; found, 338.0761, [M + Na]+, calcd 360.0567; found, 360.0571, [M + K]+, calcd 376.0306; found, 376.0296.

General Procedure B

The isoindolin-1-one derivative (0.1 g; 0.3 mmol) was dissolved in 10 mL of 5% KOH in MeOH, and the mixture was heated for 30 min. The color of the solution turned brown, the reaction was quenched with water, and extraction with ethyl acetate was performed. The organic layer was then dried over anhydrous MgSO4, and the solvent was evaporated under reduced pressure. The resulting product was purified and identified as the cinnoline or benzotriazine ester.

General Procedure C

The isoindolin-1-one derivative (0.1 g; 0.3 mmol) was dissolved in 10 mL of 5% KOH in MeOH, and the mixture was heated for 30 min. The color of the solution turned brown, the reaction was quenched with water, and extraction with ethyl acetate was performed. The aqueous layer was then acidified with concentrated HCl. The crude precipitate was filtrated using a Buchner funnel. The product was recrystallized in 2 mL of methanol, collected by vacuum filtration, and washed with cold methanol and identified as the cinnoline or benzotriazine acid.

Methyl 2-(4-Cyanocinnolin-3-yl)benzoate (14)

This product was synthesized according to general procedure B. It was purified by recrystallization in 2 mL of ethanol and collected by filtration as yellow crystals (0.62 mg; 60%). Melting point: 144 °C; 1H NMR (500 MHz, CDCl3): δ 8.72–8.74 (m, 1H), 8.21–8.23 (m, 2H), 8.00–8.02 (m, 2H), 7.77 (dt, J = 7.5, 1.0 Hz, 1H), 7.66–7.71 (m, 2H), 3.70 (s, 3H); 13C NMR (126 MHz, CDCl3): δ 166.67, 156.64, 148.74, 136.69, 134.13, 132.47, 131.77, 131.45, 131.09, 130.47, 130.30, 124.23, 123.87, 114.04, 106.84, 52.40 ppm; DEPT 135 (126 MHz, CDCl3): δ 134.13, 132.47, 131.77, 131.45, 131.09, 130.96, 130.30, 124.23, 52.41; FTIR (cm–1): 1716 (s), 1564 (w), 1434 (w), 1294 (w), 1272 (s), 1128 (m), 1084 (m), 1064 (w), 1048 (w), 1030 (m), 772 (s), 771 (m); m/z: calcd for C17H11N3O2 [M + H]+, 290.0924; found, 290.0921, [M + Na]+, calcd 312.07435; found, 312.0741, [M + K]+, calcd 328.04828; found, 328.0484.

2-(4-Cyanocinnolin-3-yl)benzoic Acid (15)

This product was synthesized according to general procedure C as yellow crystals (0.33 mg; 34%). Melting point: 205 °C; 1H NMR (500 MHz, CDCl3): δ 8.71–8.72 (m, 1H), 8.24 (d, J = 8 Hz, 1H), 8.19–8.22 (m, 1H), 8.00–8.02 (m, 2H), 7.78 (dt, J = 7.25, 1.0 Hz, 1H), 7.69 (d, J = 8 Hz, 1H), 7.65 (dt, J = 8.0, 0.5 Hz, 1H); 13C NMR (126 MHz, CDCl3): δ 169.46, 156.45, 148.70, 136.91, 134.17, 133.02, 131.84, 131.78, 131.57, 130.89, 130.35, 129.63, 124.24, 123.95, 113.95, 106.99 ppm; DEPT 135 (126 MHz, CDCl3): δ 134.18, 133.03, 131.85, 131.79, 131.57, 130.89, 130.36, 124.25; FTIR (cm–1): 1700 (w), 1684 (s), 1679 (s), 1673 (s), 1662 (s), 1279 (m), 1148 (w), 1136 (w), 727 (s); m/z: calcd for C16H9N3O2 [M + H]+, 276.07675; found, 276.0766, [M + Na]+, calcd 298.0587; found, 298.0587, [M + K]+, calcd 314.03263; found, 314.0241.

Methyl 2-(benzo[e][1,2,4]triazin-3-yl)benzoate (16a)

This product was synthesized according to general procedure B. It was purified by recrystallization in 2 mL of ethanol and collected by filtration as yellow crystals (0.46 mg; 45%). Melting point: 145 °C; 1H NMR (500 MHz, CDCl3): δ 8.59 (qd, J = 8.5, 0.5 Hz, 1H), 8.21 (dd, J = 7.5, 1.0 Hz, 1H), 8.11 (qd, J = 8.5, 0.5 Hz, 1H), 8.00–8.03 (m, 1H), 7.89–7.92 (m, 2H), 7.71 (dt, J = 7.5, 1.5 Hz, 1H), 7.64 (dt, J = 7.5, 1.5 Hz, 1H), 3.73 (s, 3H); 13C NMR (126 MHz, CDCl3): δ 169.04, 161.41, 145.94, 140.61, 136.44, 135.68, 132.83, 131.38, 130.89, 130.69, 130.27, 129.68, 129.68, 128.99, 52.31 ppm; DEPT 135 (126 MHz, CDCl3): δ 135.68, 131.38, 130.89, 130.70, 130.27, 129.68, 129.68, 128.99, 52.31; FTIR (cm–1): 2923 (w), 1735 (s), 1683 (m), 1625 (w), 1604 (w), 1572 (w), 1524 (m), 1509 (w), 1260 (w), 1096 (w), 867 (w), 778 (m), 743 (m), 705 (s); m/z: calcd for C15H11N3O2 [M + H]+, 266.0924; found, 266.0926, [M + Na]+, calcd 288.07435; found, 288.0743, [M + K]+, calcd 304.04828; found, 304.0485.

2-(Benzo[e][1,2,4]triazine-3-yl)benzoic Acid (17a)

This product was synthesized according to the general procedure C as yellow crystals (0.48 mg; 51%). Melting point: 180 °C; 1H NMR (500 MHz, CDCl3): δ 8.54 (dd, J = 8.5, 0.5 Hz, 1H), 8.10 (d, J = 8.5 Hz, 2H), 7.97–8.01 (m, 2H), 7.86–7.89 (m, 1H), 7.73 (dt, J = 7.5, 1.0 Hz, 1H), 7.63 (dt, J = 7.5, 1.0 Hz, 1H); 13C NMR (126 MHz, CDCl3): δ 172.25, 161.55, 145.85, 140.60, 136.97, 135.83, 131.99, 131.77, 131.15, 130.83, 130.43, 130.19, 129.56, 128.97 ppm; DEPT 135 (126 MHz, CDCl3): δ 135.83, 131.99, 131.15, 130.83, 130.43, 130.19, 129.55, 128.96; FTIR (cm–1): 2928 (w), 1705 (s), 1489 (w), 1451 (w), 1391 (w), 1238 (s) 1120 (m), 1015 (m), 1003 (m), 806 (m), 775 (s), 762 (s), 726 (s), 631 (m); m/z: calcd for C14H9N3O2 [M + H]+, 252.07675; found, 252.0767, [M + Na]+, calcd 274.0587; found, 274.0587, [M + K]+, calcd 290.03263; found, 290.0243.

Methyl 2-(7-Methylbenzo[e][1,2,4]triazin-3-yl)benzoate (16b)

This product was synthesized according to general procedure B. It was purified by recrystallization in 2 mL of ethanol and collected by filtration as yellow crystals (0.20 mg; 20%). Melting point: 143 °C; 1H NMR (500 MHz, CDCl3): δ 8.33 (s, 1H), 8.20 (dd, J = 8.0, 1.0 Hz, 1H), 7.99 (d, J = 8.5 Hz, 1H), 7.88 (dd, J = 8.0, 1.5 Hz, 1H), 7.84 (dd, J = 8.5, 2.0 Hz, 1H), 7.70 (dt, J = 7.5, 1.5 Hz, 1H), 7.62 (dt, J = 7.5, 1.0 Hz, 1H), 3.72 (s, 3H), 2.68 (s, 3H); 13C NMR (126 MHz, CDCl3): δ 169.17, 160.95, 145.98, 141.65, 139.33, 138.29, 136.49, 132.82, 131.29, 130.77, 130.10, 129.61, 128.45, 127.88, 52.26, 22.05 ppm; DEPT 135 (126 MHz, CDCl3): δ 138.29, 131.29, 130.77, 130.10, 129.60, 128.45, 127.88, 52.26, 22.05; FTIR (cm–1): 1727 (s), 1558 (m), 1501 (m), 1431 (m), 1417 (m), 1318 (m), 1287 (s), 1249 (m), 1119 (m), 1087 (m), 827 (m), 734 (s); m/z: calcd for C16H13N3O2 [M + H]+, 280.10805; found, 280.1078, [M + Na]+, calcd 302.0900; found, 302.0898, [M + K]+, calcd 318.06393; found, 318.0640.

2-(7-Methylbenzo[e][1,2,4]triazin-3-yl)benzoic Acid (17b)

This product was synthesized according to general procedure C as yellow crystals (0.58 mg; 61%). Melting point: 196 °C; 1H NMR (500 MHz, CDCl3): δ 8.30 (d, J = 0.5 Hz, 1H), 8.13 (dd, J = 7.5, 0.5 Hz, 1H), 8.01 (t, J = 9.0 Hz, 2H), 7.83 (dd, J = 8.5, 1.5 Hz, 1H), 7.73 (dt, J = 7.5, 1.5 Hz, 1H), 7.63 (dt, J = 7.5, 0.5 Hz, 1H), 2.97 (s, 3H); 13C NMR (126 MHz, CDCl3): δ 171.60, 161.04, 145.93, 141.91, 139.33, 138.54, 136.92, 131.96, 161.67, 131.16, 130.56, 130.10, 128.40, 127.78, 22.06 ppm; DEPT 135 (126 MHz, CDCl3): δ 138.54, 131.96, 131.16, 130.56, 130.10, 128.40, 127.78, 22.07; FTIR (cm–1): 1690 (m), 1653 (w), 1263 (m), 1007 (w), 836 (m), 761 (m), 710 (w), 672 (w); m/z: calcd for C15H11N3O2 [M + H]+, 266.0924; found, 266.0925, [M + Na]+, calcd 288.07435; found, 288.0744, [M + K]+, calcd 304.04828; found, 304.0413.

Methyl 2-(6,7-Dimethylbenzo[e][1,2,4]triazin-3-yl)benzoate (16c)

This product was synthesized according to general procedure B. It was purified by silica gel column chromatography (9:1 hexane/ethyl acetate) and obtained as a yellow solid (0.48 mg; 48%). Melting point: 150 °C; 1H NMR (500 MHz, CDCl3): δ 8.28 (s, 1H), 8.20 (dd, J = 8.0, 1.0 Hz, 1H), 7.87 (dd, J = 7.7, 1.0 Hz, 1H), 7.82 (s, 1H), 7.68 (dt, J = 7.5, 1.5 Hz, 1H), 7.60 (dt, J = 7.6, 1.5 Hz, 1H), 3.71 (s, 3H), 2.58 (s, 3H), 2.56 (s, 3H); 13C NMR (126 MHz, CDCl3): δ 169.30, 160.93, 147.74, 145.40, 141.94, 139.90, 136.62, 132.83, 131.22, 130.71, 129.99, 129.53, 128.05, 127.45, 52.26, 21.11, 20.55 ppm; DEPT 135 (126 MHz, CDCl3): δ 131.22, 130.71, 129.99, 129.52, 128.04, 127.45, 52.26, 21.11, 20.55; FTIR (cm–1): 2923 (m), 1723 (s), 1456 (w), 1377 (w), 1331 (w), 1286 (m), 1249 (w), 1114 (m), 1089 (m), 1049 (m), 1023 (w), 999 (w), 862 (w), 771 (m), 719 (s), 706 (w);m/z: calcd for C17H15N3O2 [M + H]+, 294.1237; found, 294.1234, [M + Na]+, calcd 316.10565; found, 316.1056, [M + K]+, calcd 332.07958; found, 322.0797.

2-(6,7-Dimethylbenzo[e][1,2,4]triazin-3-yl)benzoic Acid (17c)

This product was synthesized according to general procedure C as yellow crystals (0.32 mg; 34%). Melting point: 214 °C; 1H NMR (500 MHz, CDCl3): δ 8.28 (s, 1H), 8.20 (dd, J = 7.5, 1.0 Hz, 1H), 8.07 (dd, J = 7.5, 1.0 Hz, 1H), 7.85 (s, 1H), 7.73 (dt, J = 7.6, 1.5 Hz, 1H), 7.64 (dt, J = 7.6, 1.0 Hz, 1H), 2.58 (s, 3H), 2.56 (s, 3H); 13C NMR (126 MHz, CDCl3): δ 170.87, 160.94, 148.27, 145.37, 142.36, 139.81, 136.76, 131.90, 131.77, 131.25, 130.82, 130.10, 127.96, 127.33, 21.11, 20.57 ppm; DEPT 135 (126 MHz, CDCl3): δ 131.89, 131.25, 130.82, 130.09, 127.95, 127.32, 21.11, 20.57; FTIR (cm–1): 2925 (w), 1706 (s), 1653 (w), 1468 (w), 1442 (w), 1332 (w), 1260 (w), 1220 (m), 1126 (m), 1020 (w), 997 (w), 870 (m), 794 (m), 771 (s), 754 (w), 724 (s), 668 (s), 634 (m); m/z: calcd for C16H13N3O2 [M + H]+, 280.10805; found, 280.1078, [M + Na]+, calcd 302.0900; found, 302.0899, [M + K]+, calcd 318.06393; found, 318.0602.

Methyl 2-(7-Methoxybenzo[e][1,2,4]triazin-3-yl)benzoate (16d)

3-((4-Methoxy-2-nitrophenyl)amino)isoindolin-1-one 10d (0.1 g, 0.3 mmol) was dissolved in 10 mL of 5% KOH in MeOH, and the mixture was heated for 15 min. The color of the solution turned orange, the reaction was quenched with water, and extraction with ethyl acetate was performed. The organic layer was then dried with anhydrous MgSO4, and the solvent was evaporated under reduced pressure. The product was recrystallized in 2 mL of ethanol and collected by filtration as orange crystals (0.54 mg; 54%). Melting point: 151 °C; 1H NMR (500 MHz, CDCl3): δ 8.21 (dd, J = 7.5, 1.0 Hz, 1H), 7.99 (d, J = 9.5 Hz, 1H), 7.90 (dd, J = 7.5, 1.0 Hz, 1H), 7.78 (d, J = 2.5 Hz, 1H), 7.71 (dt, J = 7.5, 1.5, 1H), 7.67 (dd, J = 9.5, 2.5, 1H), 7.63 (dt, J = 7.5, 1.0 Hz, 1H), 4.09 (s, 3H), 3.75 (s, 3H); 13C NMR (126 MHz, CDCl3): δ 169.24, 161.03, 160.36, 147.33, 137.72, 136.50, 132.70, 131.27, 130.62, 130.35, 129.99, 129.94, 129.58, 105.05, 56.23, 52.25 ppm; DEPT 135 (126 MHz, CDCl3): δ 131.27, 130.62, 130.35, 129.99, 129.94, 129.58, 56.23, 52.25; FTIR (cm–1): 1726 (s), 1618 (w), 1506 (w), 1426 (s), 1290 (m), 1254 (w), 1199 (s), 1171 (w), 1089 (s), 1015 (m), 838 (s), 776 (m), 763 (s), 737 (m), 696 (m), 604 (s); m/z: calcd for C16H13N3O3 [M + H]+, 296.1029; found, 296.1027, [M + Na]+, calcd 318.0850; found, 318.0848, [M + K]+, calcd 334.0589; found, 334.0588.

2-(7-Methoxybenzo[e][1,2,4]triazin-3-yl)benzoic Acid (17d)

3-((4-Methoxy-2-nitrophenyl)amino)isoindolin-1-one 10d (0.1 g, 0.3 mmol) was dissolved in 10 mL of 5% KOH in MeOH, and the mixture was heated for 15 min. The color of the solution turned orange, the reaction was quenched with water, and extraction with ethyl acetate was performed. The aqueous layer was then acidified with concentrated HCl and extracted again with ethyl acetate. The latter was dried with anhydrous MgSO4, and the solvent was evaporated under reduced pressure. The product was recrystallized in 2 mL of methanol and collected by filtration as yellow crystals (0.40 mg; 42%). Melting point: 230 °C; 1H NMR (500 MHz, DMSO-d6): δ 12.88 (s, 1H), 8.08 (d, J = 9.5 Hz, 1H), 7.96 (dd, J = 7.5, 1.0 Hz, 1H), 7.92 (d, J = 2.5 Hz, 1H), 7.89 (dd, J = 7.5, 1.0 Hz, 1H), 7.85 (dd, J = 9.0, 2.5 Hz, 1H), 7.76 (dt, J = 7.5, 1.5 Hz, 1H), 7.69 (dt, J = 7.5, 1.0 Hz, 1H), 4.05 (s, 3H); 13C NMR (126 MHz, DMSO-d6): δ 169.55, 161.32, 161.06, 147.27, 137.31, 137.10, 133.85, 131.69, 131.05, 131.02, 130.40, 130.35, 129.78, 105.46, 56.92 ppm; DEPT 135 (126 MHz, DMSO-d6): δ 131.70, 131.05, 131.02, 130.40, 130.35, 129.78, 105.46, 56.92; FTIR (cm–1): 1705 (s), 1620 (w), 1501 (m), 1432 (m), 1288 (w), 1228 (s), 1204 (s), 1178 (w), 1117 (m), 1042 (m), 1015 (s), 850 (s), 773 (s), 723 (m), 668 (m); m/z: calcd for C15H11N3O3 [M + H]+, 282.0867; found, 282.0870, [M + Na]+, calcd 304.0692; found, 304.0692, [M + K]+, calcd 320.0432; found, 320.0368.

Methyl 2-(6-Methoxybenzo[e][1,2,4]triazin-3-yl)benzoate (16e)

3-((5-Methoxy-2-nitrophenyl)amino)isoindolin-1-one 10e (0.1 g, 0.3 mmol) was dissolved in 10 mL of 5% KOH in MeOH, and the mixture was heated for 15 min. The color of the solution turned light brown, the reaction was quenched with water, and extraction with ethyl acetate was performed. The organic layer was then dried by anhydrous MgSO4, and the solvent was evaporated under reduced pressure. The product was purified by silica gel column chromatography (6:4 hexane/ethyl acetate) and obtained as an oily/sticky brown solid (0.48 mg; 47%). 1H NMR (500 MHz, CDCl3): δ 8.39 (d, J = 9.5 Hz, 1H), 8.15 (dd, J = 7.5, 1.0 Hz, 1H), 7.89 (dd, J = 7.5, 1.0 Hz, 1H), 7.69 (dt, J = 7.5, 1.0 Hz, 1H), 7.61 (dt, J = 7.5, 1.5 Hz, 1H), 7.49 (dd, J = 10.0, 2.5 Hz, 1H), 7.24 (d, J = 2.5 Hz, 1H), 4.03 (s, 3H), 3.72 (s, 3H); 13C NMR (126 MHz, CDCl3): δ 169.13, 165.18, 161.70, 143.67, 143.52, 136.79, 132.75, 131.29, 130.95, 130.72, 130.07, 129.61, 125.33, 104.56, 56.33, 52.28 ppm; DEPT 135 (126 MHz, CDCl3): δ 131.29, 130.95, 130.72, 130.07, 129.61, 125.33, 104.56, 56.33, 52.28; FTIR (cm–1): 1724 (s), 1615 (s), 1510 (w), 1468 (s), 1432 (w), 1410 (s), 1318 (w), 1291 (m), 1241 (w), 1219 (s), 1180 (w), 1113 (m), 1088 (m), 1048 (w), 1013 (m), 836 (m), 770 (m), 728 (s), 708 (m); m/z: calcd for C16H13N3O3 [M + H]+, 296.10297; found, 296.1027, [M + Na]+, calcd 318.0849; found, 318.0850, [M + K]+, calcd 334.0588; found, 334.0590.

2-(6-Methoxybenzo[e][1,2,4]triazin-3-yl)benzoic Acid (17e)

3-((5-Methoxy-2-nitrophenyl) amino)isoindolin-1-one 10e (0.1 g, 0.3 mmol) was dissolved in 10 mL of 5% KOH in MeOH, and the mixture was heated for 15 min. The color of the solution turned light brown, the reaction was quenched with water, and extraction with ethyl acetate was performed. The aqueous layer was then acidified with concentrated HCl and extracted again with ethyl acetate. The latter was dried with anhydrous MgSO4, and the solvent was evaporated under reduced pressure. The product was recrystallized in 2 mL of methanol and collected by filtration as yellow crystals (0.43 mg; 45%). Melting point: 212 °C; 1H NMR (500 MHz, DMSO-d6): δ 12.90 (s, 1H), 8.46 (d, J = 9.5 Hz, 1H), 7.93 (dd, J = 7.5, 1.0 Hz, 1H), 7.89 (dd, J = 7.5, 1.0 Hz, 1H), 7.75 (dt, J = 7.5, 1.5 Hz, 1H), 7.66–7.71 (m, 2H), 7.44 (d, J = 2.5 Hz, 1H), 4.05 (s, 3H); 13C NMR (126 MHz, DMSO-d6): δ; 168.30, 164.38, 161.36, 142.39, 142.23, 136.30, 132.88, 130.52, 129.94, 129.94, 129.35, 128.67, 124.91, 104.27, 56.12 ppm; DEPT 135 (126 MHz, DMSO-d6): δ 130.52, 129.94, 129.94, 129.36, 128.67, 124.91, 104.27, 56.12; FTIR (cm–1): 1717 (s), 1615 (s), 1469 (s), 1319 (w), 1221 (m), 1179 (w), 1116 (m), 1089 (w), 1013 (m), 837 (m), 769 (m), 726 (m); m/z: calcd for C15H11N3O2 [M + H]+, 282.08732; found, 282.0872, [M + Na]+, calcd 304.06926; found, 304.0694, [M + K]+, calcd 320.0432; found, 320.0400.

Methyl 2-(7-Chlorobenzo[e][1,2,4]triazin-3-yl)benzoate (16f)

This product was synthesized according to general procedure B. It was purified by recrystallization in 2 mL of ethanol and collected by filtration as orange crystals (0.82 mg; 78%). Melting point: 113 °C; 1H NMR (500 MHz, CDCl3): δ 8.58 (d, J = 2.0 Hz, 1H), 8.18 (dd, J = 7.5, 1.0 Hz, 1H), 8.06 (d, J = 9.0 Hz, 1H), 7.94 (dd, J = 9.0, 2.5 Hz, 1H), 7.91 (dd, J = 7.5, 1.0 Hz, 1H), 7.72 (dt, J = 7.5, 1.5 Hz, 1H), 7.65 (dt, J = 7.5, 1.5 Hz, 1H), 3.73 (s, 3H); 13C NMR (126 MHz, CDCl3): δ 168.87, 161.62, 145.76, 139.24, 136.89, 136.56, 136.09, 132.79, 131.44, 130.88, 130.53, 130.48, 129.77, 128.25, 52.34 ppm; DEPT 135 (126 MHz, CDCl3): δ 136.90, 131.44, 130.88, 130.53, 130.48, 129.77, 128.25, 52.34; FTIR (cm–1): 1729 (s), 1689 (w), 1506 (m), 1413 (m), 1288 (s), 1118 (m), 1084 (m), 1043 (w), 1011 (m), 902 (m), 849 (m), 839 (m), 774 (m), 741 (m), 721 (s), 705 (m); m/z: calcd for C15H10ClN3O2 [M + H]+, 300.05343; found, 300.0534, [M + Na]+, calcd 322.03537; found, 322.0351, [M + K]+, calcd 338.00931; found, 338.0094.

2-(7-Chlorobenzo[e][1,2,4]triazin-3-yl)benzoic Acid (17f)

This product was synthesized according to general procedure C as yellow crystals (0.19 mg; 19%). Melting point: 177 °C; 1H NMR (500 MHz, CDCl3): δ 8.53 (d, J = 2.5 Hz, 1H), 8.04–8.09 (m, 2H), 8.00 (d, J = 7.5 Hz, 1H), 7.92 (dd, J = 9.0, 2.0 Hz, 1H), 7.74 (dt, J = 7.5, 1.0 Hz, 1H), 7.65 (dt, J = 7.5, 1.0 Hz, 1H); 13C NMR (126 MHz, CDCl3): δ 172.14, 161.77, 145.70, 139.24, 137.01, 136.74, 136.70, 132.09, 131.63, 131.10, 130.56, 130.43, 130.38, 128.10 ppm; DEPT 135 (126 MHz, CDCl3): δ 137.01, 132.09, 131.10, 130.56, 130.43, 130.38, 128.11; FTIR (cm–1): 1704 (s), 1488 (w), 1431 (w), 1417 (w), 1224 (s), 1206 (m), 1117 (m), 1043 (m), 1019 (m), 1006 (m), 847 (s), 804 (w), 772 (s), 720 (m), 668 (s), 652 (m), 647 (m), 636 (m); m/z: calcd for C14H8ClN3O2 [M + H]+, 286.03778; found, 286.0378, [M + Na]+, calcd 308.01972; found, 308.0198, [M + K]+, calcd 323.99366; found, 323.0094.

Methyl 2-(7-Chloro-6-methoxybenzo[e][1,2,4]triazin-3-yl)benzoate (16g)

This product was synthesized according to general procedure B. It was purified by recrystallization in 2 mL of ethanol and collected by filtration as yellow crystals (0.42 mg; 42%). Melting point: 165 °C; 1H NMR (500 MHz, CDCl3): δ 8.55 (s, 1H), 8.13 (dd, J = 8.0, 1.0 Hz, 1H), 7.90 (dd, J = 8.0, 1.0 Hz, 1H), 7.69 (dt, J = 7.6, 1.5 Hz, 1H), 7.62 (dt, J = 7.6, 1.5 Hz, 1H), 7.33 (s, 1H), 4.13 (s, 3H), 3.72 (s, 3H); 13C NMR (126 MHz, CDCl3): δ 168.99, 161.78, 160.67, 142.73, 142.12, 136.49, 132.69, 131.37, 130.70, 130.25, 130.20, 129.87, 129.70, 105.74, 57.25, 52.32 ppm; DEPT 135 (126 MHz, CDCl3): δ 131.37, 130.70, 130.25, 129.87, 129.70, 105.74, 57.25, 52.33; FTIR (cm–1): 1727 (s), 1695 (w), 1602 (w), 1474 (m), 1410 (m), 1282 (m), 1242 (w), 1226 (m), 1116 (w), 1089 (m), 1040 (m), 1023 (w), 999 (w), 880 (w), 841 (m), 732 (s); m/z: calcd for C16H12ClN3O3 [M + H]+, 330.0640; found, 330.0637, [M + Na]+, calcd 352.04594; found, 352.0459, [M + K]+, calcd 368.01988; found, 368.0198.

2-(7-Chloro-6-methoxybenzo[e][1,2,4]triazin-3-yl)benzoic Acid (17g)

This product was synthesized according to general procedure C as yellow crystals (0.46 mg; 48%). Melting point: 215 °C; 1H NMR (500 MHz, CDCl3): δ 8.49 (s, 1H), 8.11 (dd, J = 8.0, 1.0 Hz, 1H), 7.98 (dd, J = 7.5, 1.0 Hz, 1H), 7.72 (dt, J = 7.6, 1.5 Hz, 1H), 7.63 (dt, J = 7.6, 1.0 Hz, 1H), 7.37 (s, 1H), 4.03 (s, 3H); 13C NMR (126 MHz, CDCl3): δ 171.88, 161.63, 160.82, 142.71, 142.11, 136.68, 131.91, 131.86, 131.03, 130.49, 130.42, 130.29, 129.71, 105.79, 57.23 ppm; DEPT 135 (126 MHz, CDCl3): δ 131.92, 131.03, 130.42, 130.29, 129.71, 105.76, 57.23; FTIR (cm–1): 1705 (s), 1598 (w), 1474 (s), 1413 (s), 1264 (m), 1244 (s), 1225 (m), 1123 (w), 1041 (m), 1021 (m), 997 (m), 768 (s); m/z: calcd for C15H10ClN3O3 [M + H]+, 316.04835; found, 316.0483 [M + Na]+, calcd 338.03029; found, 338.0305, [M + K]+, calcd 354.00423; found, 353.9991.

Methyl 2-(7-(Trifluoromethyl)benzo[e][1,2,4]triazin-3-yl)benzoate (16h)

This product was synthesized according to general procedure B. It was purified by silica gel column chromatography (9:1 hexane/ethyl acetate) and obtained as an oily/sticky yellow solid (0.44 mg, 44%). 1H NMR (500 MHz, CDCl3): δ 8.91 (s, 1H), 8.24 (d, J = 9 Hz, 1H), 8.18 (d, J = 7.5 Hz, 1H), 8.16 (dd, J = 8.75, 2.0 Hz, 1H), 7.94 (d, J = 7.5 Hz, 1H), 7.73 (t, J = 7.5 Hz, 1H), 7.67 (t, J = 8 Hz, 1H), 3.74 (s, 3H); 13C NMR (126 MHz, CDCl3): δ 168.69, 162.71, 144.65, 141.56, 135.91, 132.87, 132.22, 131.56, 131.06, 130.81, 130.72, 129.88, 127.92, 124.10, 121.93, 52.40 ppm; DEPT 135 (126 MHz, CDCl3): δ 132.87, 132.22, 131.56, 131.06, 130.81, 130.72, 129.89, 127.92, 52.40; FTIR (cm–1): 1731 (s), 1684 (m), 1561 (m), 1421 (m), 1322 (s), 1186 (m), 1149 (m), 1122 (s), 1092 (m), 1056 (m), 772 (m), 745 (m), 708 (s), 614 (s); m/z: calcd for C16H10F3N3O2 [M + H]+, 334.07979; found, 334.0796, [M + Na]+, calcd 356.06173; found, 356.0614, [M + K]+, calcd 372.03567; found, 372.0358.

2-(7-(Trifluoromethyl)benzo[e][1,2,4]triazin-3-yl)benzoic Acid (17h)

This product was synthesized according to general procedure C as yellow crystals (0.49 mg; 51%). Melting point: 161 °C; 1H NMR (500 MHz, CDCl3): δ 8.88 (s, 1H), 8.27 (d, J = 8.5 Hz, 1H), 8.16 (dd, J = 9.0, 1.5 Hz, 1H), 8.12 (d, J = 7.5 Hz, 1H), 8.04 (d, J = 7.5 Hz, 1H), 7.77 (t, J = 7.5 Hz, 1H), 7.68 (t, J = 7.5 Hz, 1H); 13C NMR (126 MHz, CDCl3): δ 171.77, 162.80, 144.67, 141.55, 136.61, 132.35, 132.27, 131.50, 131.30, 131.16, 130.76, 130.71, 130.53, 127.87, 127.84 ppm; DEPT 135 (126 MHz, CDCl3): δ 132.28, 131.32, 131.18, 130.77, 130.71, 130.54, 127.87; FTIR (cm–1): 1722 (m), 1423 (w), 1323 (s), 1235 (m), 1188 (m), 1155 (w), 1123 (s), 1057 (w), 1009 (w), 847 (m), 771 (m), 730 (m), 654 (m); m/z: calcd for C15H8F3N3O2 [M + H]+, 320.06414; found, 320.0643, [M + Na]+, calcd 342.04608; found, 342.0463, [M + K]+, calcd 358.02002; found, 358.0122.