Synthesis of New Spiro-Cyclopropanes Prepared by Non-Stabilized Diazoalkane Exhibiting an Extremely High Insecticidal Activity.

The synthesis of new insecticidal gem-dimethyspiro-cyclopropanes derived from pyrrolidine-2,3-dione have been described, and their biological effect against different insect species has been evaluated. The presented results demonstrate the excellent insecticidal activity of cyclopropane 5c against Aedes aegypti and Musca domestica. Cyclopropane 5c showed the quickest knockdown and the best killing against Aedes aegypti and Musca domestica compared to trans-chrysanthemic acid and pyrethrin. The biological results of the high insecticidal activity were confirmed by the results of docking. This is evident in the binding affinity obtained for cyclopropane 5c, indicating good binding with an important active amino acid residue of the 5FT3 protein.

1. Introduction

Cyclopropanes are one of the best-known strained rings, having attracted the attention of major researchers for over a century due to their powerful and unique reactivity. They not only exist in many natural products [1,2,3,4], but have also been frequently used in many disciplines such as organic synthesis, materials science and biology and as building blocks for general-purpose materials. During the last decade, much research has been carried out to advance original regio-chemo and stereoselective approaches for the preparation and conversions of cyclopropane derivatives [5,6,7,8,9,10]. This research has generated considerable interest since fragments of cyclopropane are present in the structures of numerous biologically active substances, such as anticancer, antibiotics and antimycotic arrangements, regulators of plant development and maturation of fruits and insecticides [11,12]. Chrysanthemic acid and pyrethrins, insecticides isolated from the flower Chrysanthemum cinerariaefolium, are traditionally cited as examples of natural bioactive cyclopropanes. Their 2-vinylcyclopropanecarboxylic structural unit has been a good source of inspiration for the development of other synthetic cyclopropane insecticides for phytopharmaceutical use, such as deltamethrin (Roussel-Uclaf) (Figure 1) [13,14,15].

Figure 1

Structures of the most active cyclopropane derivatives.

The application of spiro-cyclopropane structures in drug discovery has seen a dramatic increase in attention in recent years, alongside major developments in their synthetic chemistry [16]. Various biological activities have also been described for spiro-cyclopropane derivatives, such as anti-inflammatory and cytotoxic activity [17]. The consideration of compounds that include this structure has not been limited to molecules of synthetic origin but rather has been focused on natural products because this functionality has been described in numerous naturally occurring compounds. In the case of spiro-cyclopropanes destined for heterocycles, there are few reports of biological activity, especially the cyclopropane derivatives, which have been used as fungicides, pesticides and insecticides [18,19].

Photochemical diazotization of 1-pyrazoline derivatives is a widely used process in organic preparation to synthesize cyclopropane derivatives [20,21]. Pyrazoline derivatives are presently formed by 1,3-dipolar cycloaddition reactions of diazoalkanes to electron-deficient alkenes [22,23,24,25]. The current work describes the synthesis of spiro-cyclopropane derivatives via the photolysis of pyrazolines obtained by the cycloaddition of diazopropane with (E)-4-arylidene-pyrrolidine-2,3-dione derivatives. This reaction is based on the cycloaddition of diazopropane, generated in the initial oxidative addition step with iodosylbenzene.

2. Results and Discussion

2.1. Synthesis of New Spiro-Cyclopropane

The starting materials 1 was prepared by condensing acetone azine with hydrazine [26], and (E)-4-benzylidene-1-phenylpyrrolidine-2,3-dione derivatives 3a–d were synthesized by the reaction between 1-arylpyrrolidine-2,3-diones and aldehydes, as described in the literature [27,28,29,30]. Diazopropane 2 was prepared in situ by oxidizing acetone azine using iodosylbenzene according to the literature procedure [31]. 1,3-dipolar cycloadditions of 2-diazopropane 2 to (E)-4-benzylidene-1-phenylpyrrolidine-2,3-dione derivatives 3a–d readily occur in dichloromethane at −40 °C. The reaction medium is left stirring for one hour at this temperature, then brought back to 0 °C gradually in a cryostat (Scheme 1) [32].

Scheme 1

Synthesis and evolution of spiro pyrazole derivatives by cycloaddition of (E)-4-arylidene-pyrrolidine-2,3-dione derivatives with 2-diazopropane prepared by oxidizing with iodosylbenzene.

The 1,3-dipoar cycloaddition of 2-diazopropane is, in each case, regiospecific. The chemical shifts of C5 (99.4 to 99.7 ppm) are in excellent agreement with those usually obtained when this quaternary carbon is attached to the nitrogen atom [25]. The FT-IR spectra of all the synthesized pyrazolines 4a–d showed absorption bands in the range of 1525–1530 cm−1 for the azo group (N=N). The formation of the five-membered ring cycle was confirmed by the presence of two methylene protons for the pyrazoline ring. The chemical shifts of two methylene protons of the compounds 4a–d were observed between 1.26 and 129 ppm and 1.72–1.79 ppm. One prominent doublet δ = 2.90–3.25 ppm, J = 18.3 Hz appeared in the 1H-NMR spectra of pyrazolines 4a–d, which corresponds to the hydrogen atoms H-9. The chemical shifts of the singlet corresponding to the hydrogen atom H-4 appeared at 3.54–3.59 ppm. The chemical shifts of the aromatic protons were found between 6.87 and 7.50 ppm. The 13C-NMR of pyrazolines 4a–d revealed carbonyl carbon peaks at 114.2–160.1 ppm. Aromatic carbon atom chemical shifts appeared in the range of 73.1–200.9 ppm. Under stationary irradiations, pyrazolines 4a–d yield the discount cyclopropanes 5a–d. Pyrazoline solutions contained in Pyrex reactors were irradiated with a high-pressure mercury lamp (125 W). The formation of spiro-cyclopropanes 5a–d was confirmed by 13C-NMR. The C-3 spiranic carbon chemical shifts of compounds 5a–d were observed between 34.0 and 34.3 ppm, confirming that the carbon is not attached to the nitrogen atom. In all cases, we used benzophenone as a sensitizer and dichloromethane as the solvent. Yields were excellent for the breakdown of all pyrazolines (Scheme 1) [25,31].

2.2. Biological Activity

The preliminary screening is shown in Table 1. As presented, a number of four spiro-cyclopropanes derivatives were tested against Aedes aegypti using acetone as solvent at different concentrations (0.01, 0.005 and 0.001%) and compared to trans-chrysanthemic acid and pyrethrin. Cyclopropane derivatives 5a–d exhibit a knockdown and killing effect similar to or even superior to that of trans-chrysanthemic acid and pyrethrin (Table 1).

Table 1

Effects of cyclopropanes 5a–d, trans-chrysanthemic acid and pyrethrin at contact action against Aedes aegypti at three concentrations.

		Number of Mosquitoes that Fell on the Ground
Products	Concentration	1 min	10 min	30 min	60 min	Number of Dead Mosquitoes after 24 h
Acetone	n/a	8.3	0.3	0	0	0.6
Trans-chrysanthemic acid(Reference)	0.001	7.6	8.3	10	10	9.3
	0.005	8	9.3	10	10	10
	0.01	9.3	10	10	10	10
Pyrethrin(Reference)	0.001	8.3	8.9	10	10	10
	0.005	9.3	9.5	10	10	10
	0.01	9.5	10	10	10	10
Cyclopropane 5a	0.001	7.3	8.3	8.9	10	10
	0.005	7.8	8.5	8.9	10	10
	0.01	8.5	8.9	10	10	10
Cyclopropane 5b	0.001	7.6	8.3	8.9	10	10
	0.005	8.3	8.9	9.8	10	10
	0.01	8.6	9.3	10	10	10
Cyclopropane 5c	0.001	8.9	9.5	10	10	10
	0.005	9.3	10	10	10	10
	0.01	9.8	10	10	10	10
Cyclopropane 5d	0.001	7.3	7.6	8.3	9.3	10
	0.005	7.6	8.3	8.9	9.8	10
	0.01	8.3	8.9	9.5	10	10

Table 2 summarizes the activity results of cyclopropane derivatives 5a–c against Aedes aegypti in the vapor phase. As revealed, cyclopropane 5c exhibits higher activity than trans-chrysanthemic acid and pyrethrin. In fact, the achievement of T90 using trans-chrysanthemic acid and pyrethrin required, respectively, 40 min and 38 min, while it just needed 24 min using cyclopropane 5c.

Table 2

Effects of cyclopropanes 5a–d versus trans-chrysanthemic acid and pyrethrin in the vapor phase against Aedes aegypti.

Products (5 mg per Cellulose Paper)	Insect Exposure (h)	Knockdown Time (min)			PercentageKnockdown (8 h)	PercentageKnockdown (24 h)
		T10	T50	T90
Trans-chrysanthemic acid(reference)	0	23	31	40	100	100
	2	6	10	13	100	100
	4	5	9	12	100	100
Pyrethrin(reference)	0	21	27	38	100	100
	2	5	9	11	100	100
	4	4	8	10	100	100
Cyclopropane 5a	0	22	33	41	100	100
	2	14	23	33	100	100
	4	12	19	21	100	100
Cyclopropane 5b	0	22	32	40	100	100
	2	15	22	34	100	100
	4	12	18	19	100	100
Cyclopropane 5c	0	19	21	24	100	100
	2	4	8	10	100	100
	4	3	7	9	100	100
Cyclopropane 5d	0	25	36	45	100	100
	2	16	26	35	100	100
	4	14	21	26	100	100

Cyclopropanes 5a–d conferred a complete knockdown after 8 h and mortality after 24 h against Aedes aegypti. Additionally, the biological results registered for cyclopropanes 5b–d (Table 2) showed a slower knockdown in terms of K10, K50 and T90. In order to estimate the insecticidal activity of cyclopropane 5a–d as space spray against Aedes aegypti and Musca domestica, supplementary evaluations were conducted, and the results are shown in Table 3. All cyclopropane derivatives conferred complete knockdown against Aedes aegypti within 1 h and mortality after 24 h. Particularly, cyclopropane 5c showed a better knockdown effect than that of trans-chrysanthemic acid and pyrethrin (Table 3).

Table 3

Biological efficacy of cyclopropanes 5a–d versus trans-chrysanthemic acid and pyrethrin as a space spray in 22.5 m3 chambers against Aedes aegypti.

Products (0.05 mg m−3)	Knockdown Time (min)			PercentageKnockdown(1 h)	PercentageKnockdown (24 h)
	T10	T50	T90
Trans-chrysanthemic acid	0 min 46 s	1 min 15 s	1 min 37 s	100	100
Pyrethrin	0 min 40 s	1 min 10 s	1 min 25 s	100	100
Cyclopropane 5a	0 min 54 s	1 min 40 s	2 min 35 s	100	100
Cyclopropane 5b	1 min 02 s	1 min 55 s	2 min 44 s	100	100
Cyclopropane 5c	0 min 37 s	1 min 00 s	1 min 20 s	100	100
Cyclopropane 5d	1 min 20 s	1 min 50 s	3 min 07 s	100	99

Cyclopropane 5c achieved the quickest knockdown and the best killing effect against Musca domestica (Table 4).

Table 4

The biological efficacy of cyclopropanes 5a–d versus trans-chrysanthemic acid and pyrethrin as a space spray in 22.5 m3 chambers against Musca domestica.

Products (0.05 mg m−3)	Knockdown Time (min)			PercentageKnockdown (1 h)	PercentageKnockdown (24 h)
	T10	T50	T90
Trans-chrysanthemic acid	5 min 36 s	7 min 20 s	10 min 07 s	100	78
Pyrethrin	5 min 13 s	6 min 30 s	8 min 09 s	100	96
Cyclopropane 5a	0 min 54 s	1 min 40 s	2 min 35 s	100	61
Cyclopropane 5b	1 min 02 s	1 min 55 s	2 min 44 s	100	63
Cyclopropane 5c	0 min 37 s	1 min 00 s	1 min 20 s	100	100
Cyclopropane 5d	1 min 20 s	1 min 50 s	3 min 07 s	100	54

2.3. Docking Studies

The objective of this part is the application of molecular docking of spiro-cyclopropane derivatives in order to find possible protein targets in which they present insecticidal activity. We examine how cyclopropanes derivatives might approach the active site of the main protease of mosquitoes (Aedes aegypti PDB: 5FT3) (Figure 2). The results showed that all selected inhibitors and drugs were in the pocket of the target proteins. Interaction results were evaluated with the docking score (S). The scoring function is used to predict the binding affinity of both ligand and target once it is docked. Inhibitors with the lowest S score tend to establish a strong interaction with proteins. The docking scores for the drugs approved antiviral activity against 5FT3 proteases were calculated using MOE, applying the same parameters as those used for computing the docking scores for the 5a–d against 5FT3 proteases in this study.

Figure 2

Protein 5FT3 (A); largest pocket 5FT3 (B).

Trans-chrysanthemic acid and pyrethrin proved to be very attractive thanks to the small doses needed to kill insects. Both trans-chrysanthemic acid and pyrethrin exhibited a good interaction with protein 5FT3. The docking of trans-chrysanthemic acid with protein 5FT3 shows two polar interactions of the oxygens of carboxylic acid with the Arg112 active amino acid residue (Figure 3A). The pyrethrin docking with protein 5FT3 presents two arene-H interactions of cyclopentane with the His41 and Phe120 active amino acid residues. In this case, the docking score was −6.6755 kcal/mol (Figure 3B).

Figure 3

Two-dimensional interaction images of docking conformations of trans-chrysanthemic acid and pyrethrin with the active proteins: (A) interaction trans-chrysanthemic acid and protein 5FT3; (B) interactions pyrethrin and protein 5FT3.

A reasonable comparative study was conducted between the spiro-cyclopropane derivatives 5a–d, trans-chrysanthemic acid and pyrethrin. Docking scores were detected for 5a–d, ranging from −5.1607 kcal/mol to −6.1161 kcal/mol. The most potent ligand, cyclopropane 5c docking with protein 5FT3, formed one polar interaction with the Arg112 active amino acid residue. Lys136 and Phe120 exhibited arene-H bonds with the proton of the benzene group and cyclopropane ring, respectively. In this case, the docking score was −6.1161 kcal/mol (Figure 4).

Figure 4

Two-dimensional interaction images of docking conformations of the cyclopropanes 5a-d with the active protein 5FT3. (A) Interaction cyclopropane 5a and protein 5FT3, (B) Interactions cyclopropane 5b and protein 5FT3, (C) Interaction cyclopropane 5c and protein 5FT3, (D) Interaction cyclopropane 5d and protein 5FT3.

The 3D image of the molecular docking of cyclopropane 5c against protein 5ft3 is shown in Figure 5. Cyclopropanes 5a and 5b formed three hydrogens bonds with the Glu116, Phe120 and His41 active amino acid residues and one H-arene interaction with His4. Cyclopropane 5d formed two H-arene interactions with His53 and Lys136 active amino acid residues.

Figure 5

The molecular docking of cyclopropane 5c against protein 5FT3.

3. Conclusions

In summary, we have established an efficient, facile and safe batch preparation of gem-dimethyl spiro-cyclopropanes through the photodenitrogenation of spiro-pyrazolines obtained by 1,3-dipolar cycloaddition of highly unstable 2-diazopropane starting from acetone hydrazone and using iodosylbenzene as a perfect oxidizing agent. The reaction of 2-diazopropane with (E)-4-benzylidene-1-phenylpyrrolidine-2,3-dione derivatives 3a–d is regiospecific. The presented results demonstrate an excellent insecticidal activity of cyclopropane 5c against mosquitoes (Aedes aegypti) and house flies (Musca domestica). This result is confirmed by virtual screening established using molecular docking, and we believe that the sipro-cyclopropane derivatives could aid in insecticidal drug discovery. This is clearly manifested in the bond affinity obtained for cyclopropane 5c, indicating good binding with the important active amino acid residue of the 5FT3 protein.

4. Experimental Section

4.1. General Information

Commercially obtainable reagents were used as-supplied or purified by standard methods where required. Non-commercial starting materials were synthesized according to literature procedures. All (E)-4-benzylidene-1-phenylpyrrolidine-2,3-dione derivatives and acetone hydrazone preparation, along with cyclopropanation reactions, were run under a nitrogen atmosphere with oven-dried glassware by means of the usual methods for manipulating air-sensitive product. Dry dichloromethane was prepared by filtration under nitrogen concluded an alumina drying column on a purification system. Thin-layer chromatography was performed on silica gel 254 plates (Merck) with UV (254 nm) visualization, whereas chromatographic separations were conducted on silica gel Si-60–7734. IR spectra (KBr) were recorded on an FTIR 5300 spectrometer. Electrospray Ionization (E.S.I.) mass spectra were measured on a Bruker MicroToF 2. NMR spectra were obtained on a Bruker AV 300 spectrometer operating at 300 MHz for 1H and at 75.47 MHz for 13C. Melting points were determined on a Buchi-510 capillary melting point apparatus. The coupling constants J are given in Hertz. The spectra were recorded in CDCl3 as solvent at room temperature. Elemental analysis was recorded on a PERKIN–ELMER 240B microanalyzer.

4.2. Synthesis of Iodosylbenzene

Iodosylbenzene diacetate (3.0 g, 9.2 mmol, 1.0 equiv) was located in a 100 mL round-bottom flask, and 55 mL of NaOH (3M, 165 mmol, 18.0 equiv) was added. The reaction mixture was stirred for 1 h. The crude product was filtered using a funnel and rinsed with water, and the residual product was then abundantly rinsed with chloroform (200 mL). After dried under reduced pressure immediate, the solid was grounded and place back under vacuum for an additional 1 h. The iodosylbenzene was therefore isolated as a yellow solid (1.6 g, 80%) [28].

4.3. Synthesis of 1,2,7-Triazaspiro[4.4]non-1-ene-8,9-Dione Derivatives ()

In a round-bottom, a threaded inlet 25 mL glass vial equipped with a magnetic bar stirrer was balanced iodosylbenzene (400.0 mg, 1.80 mmol, 1.5 equiv). The bottom was then covered and blushed with nitrogen for five minutes, after which dichloromethane (6 mL) was added. A freshly distillated 6 mL acetone hydrazone (1.80 mmol, 1.5 equiv) dichloromethane was then added over 60 min. The selected alkenes (1.20 mmol, 1.0 equiv) were added. The reaction mixture was vigorously stirred for an additional 30 min at −40 °C. The resulting mixture was then filtrated over celite® and abundantly rinsed with dichloromethane, trailed by evaporation under reduced pressure. The mixture was dried over anhydrous sodium sulfate, filtered and concentrated. The crude cycloadduct was then purified by silica gel chromatography to give the pyrazolines 4a–d.

4.3.1. 3,3-Dimethyl-4,7-Diphenyl-1,2,7-Triazaspiro[4.4]non-1-ene-8,9-Dione (4a)

Yield (85%), white solid. Mp = 139–140 °C, Rf = 0.27 (cyclohexane/EtOAc 3:7). IR (KBr) νmax/cm−1: 1530 (N=N). 1H NMR (300 MHz, CDCl3) δ 1.28 (s, 3H, CH3), 1.75 (s, 3H, CH3), 2.91 and 3.25 (AA’, H9, J = 18.3 Hz), 3.58 (s, 1H, H4), 6.92–7.49 (m, 10H, Harom). 13C NMR (75.47 MHz, CDCl3) δ 24.2 and 28.3 (CH3), 37.5 (C6), 52.8 (C4), 97.4 (C3), 99.4 (C5), 126.4–135.5 (Carom), 173.1 (C8), 200.2 (C9). HRMS (ESI) Calcd for C20H19N3O2 333.1477 [M+]. Found: 333.1480. Elemental analysis: C20H19N3O2 requires C, 72.05, H, 5.74, N, 12.60%; found C, 72.01, H, 5.77, N, 12.57%.

4.3.2. 4-(4-Methoxyphenyl)-3,3-Dimethyl-7-Phenyl-1,2,7-Triazaspiro[4.4]non-1-ene-8,9-Dione (4b)

Yield (80%), white solid. Mp = 112–113 °C, Rf = 0.27 (cyclohexane/EtOAc 3:7). IR (KBr) νmax/cm−1: 1525 (N=N). 1H NMR (300 MHz, CDCl3) δ 1.26 (s, 3H, CH3), 1.72 (s, 3H, CH3), 2.92 and 3.20 (AA’, H6, J = 18.3 Hz), 3.54 (s, 1H, H4), 3.80 (s, 3H, OCH3), 6.87–7.50 (m, 9H, Harom). 13C NMR (75.47 MHz, CDCl3) δ 24.1 and 28.1 (CH3), 37.3 (C6), 52.1 (C4), 97.0 (C3), 99.2 (C5), 114.2–159.2 (Carom), 173.1 (C8), 200.3 (C9). HRMS (ESI) Calcd for C21H21N3O3 363.1583 [M+]. Found: 363.1590. Elemental analysis: C21H21N3O3 requires C, 69.41; H, 5.82; N, 11.56%; found C, 69.38; H, 5.88; N, 11.51%.

4.3.3. 7-(4-Methoxyphenyl)-3,3-Dimethyl-4-Phenyl-1,2,7-Triazaspiro[4.4]non-1-ene-8,9-Dione (4c)

Yield (75%), white solid. Mp = 123–124 °C, Rf = 0.29 (cyclohexane/EtOAc 3:7). IR (KBr) νmax/cm−1: 1530 (N=N). 1H NMR (300 MHz, CDCl3) δ 1.29 (s, 3H, CH3), 1.76 (s, 3H, CH3), 2.90 and 3.25 (AA’, H9, J = 18.3 Hz), 3.59 (s, 1H, H4), 3.84 (s, 3H, OCH3), 6.93–7.37 (m, 9H, Harom). 13C NMR (CDCl3; 75.47 MHz) δ 23.5 and 28,6 (CH3), 37.8 (C6), 53.1 (C4), 55.9 (OCH3), 97.7 (C3), 99.7 (C5), 114.9–160.1 (Carom), 173.7 (C8) and 200.8 (C9). HRMS (ESI) Calcd for C21H21N3O3 363.1583 [M+]. Found: 363.1580. Elemental analysis: C21H21N3O3 requires C, 69.41; H, 5.82; N, 11.56%; found C, 69.39; H, 5.85; N, 11.52%.

4.3.4. 4,7-bis(4-Methoxyphenyl)-3,3-Dimethyl-1,2,7-Triazaspiro[4.4]non-1-ene-8,9-Dione (4d)

Yield (65%), white solid. Mp = 97–98 °C, Rf = 0.26 (cyclohexane/EtOAc 3:7). IR (KBr) νmax/cm−1: 1530 (N=N). 1H NMR (300 MHz, CDCl3) δ 1.27 (s, 3H, CH3), 1.74 (s, 3H, CH3), 2.92 and 3.21 (AA’, H9, J = 18.3 Hz), 3.55 (s, 1H, H4), 3.83 (s, 3H, OCH3), 3.82 (s, 3H, OCH3), 6.87–7.28 (m, 8H, Harom). 13C NMR (CDCl3; 75.47 MHz) δ 24.5 and 28.5 (CH3), 37.6 (C6), 52.5 (C4), 55.7 (OCH3), 55.9 (OCH3), 97.3 (C3), 99.4 (C5), 114.5–160.1 (Carom), 173.6 (C8) and 200.9 (C9). HRMS (ESI) Calcd for C22H23N3O4 393.1689 [M+]. Found: 393.1685. Elemental analysis: C22H23N3O4 requires C, 67.16; H, 5.89; N, 10.68%; found C, 67.19; H, 5.91; N, 10.64%.

4.4. General Procedure for the Irradiation of the Spiro-Pyrazolines ()

All irradiations were carried out using similar conditions. Five moles of pyrazoline were dissolved in ether pretreated by stirring with solid (NaCO3), filtered and flushed with nitrogen and irradiated at 5 °C for a total of 30 min or until the starting material was consumed (TLC). After this period, the solvent was removed in a vacuum without heating to give a brown oil, which was subjected to rapid silica filtration. Recrystallization from dichloromethane/light petroleum.

4.4.1. 1,1-Dimethyl-2,5-Diphenyl-5-Azaspiro[2.4]heptane-6,7-Dione (5a)

Yield (85%), white solid. Mp = 186–187 °C, Rf = 0.32 (cyclohexane/EtOAc 3:7). 1H NMR (300 MHz, CDCl3) δ 1.20 (s, 3H, CH3), 1.64 (s, 3H, CH3), 2.59 and 2.74 (AA’, H4, J = 19.2 Hz), 3.04 (s, 1H, H2), 7.14–7.53 (m, 10H, Harom). 13C NMR (CDCl3; 75.47 MHz) δ 20.7 and 20.9 (CH3), 31.3 (C4), 31.9 (C1), 34.1 (C3), 40.3 (C2), 126.7–134.3 (Carom), 175.2 (C6) 200.5 (C7). HRMS (ESI) Calcd for C20H19NO2 305.1416 [M+]. Found: 305.1410. Elemental analysis: C20H19NO2 requires C, 78.66; H, 6.27; N, 4.59%; found C, 78.68; H, 6.25; N, 4.55%.

4.4.2. 5-(4-Methoxyphenyl)-1,1-Dimethyl-2-Phenyl-5-Azaspiro[2.4]heptane-6,7-Dione (5b)

Yield (90%), white solid. Mp = 145–146 °C, Rf = 0.31 (cyclohexane/EtOAc 3:7). 1H NMR (300 MHz, CDCl3) δ 1.12 (s, 3H, CH3), 1.64 (s, 3H, CH3), 2.59 and 2.74 (AA’, H74 J = 19.2 Hz), 3.04 (s, 1H, H2), 3.85 (s, 3H, OCH3), 7.00–7.40 (m, 9H, Harom). 13C NMR (CDCl3; 75.47 MHz) δ 21.1 and 21.2 (CH3), 31.6 (C4), 32.1 (C1), 34.3 (C3), 40.5 (C2), 55.9 (OCH3), 114.8–159.8 (Carom), 175.9 (C6) 200.2 (C7). HRMS (ESI) Calcd for C21H21NO3 335.1521 [M+]. Found: 335.1525. Elemental analysis: C21H21NO3 requires C, 75.20; H, 6.31; N, 4.18%; found C, C, 75.18; H, 6.29; N, 4.20%.

4.4.3. 2-(4-Methoxyphenyl)-1,1-Dimethyl-5-Phenyl-5-Azaspiro[2.4]heptane-6,7-Dione (5c)

Yield (75%), white solid. Mp = 151–153 °C, Rf = 0.31 (cyclohexane/EtOAc 3:7). 1H NMR (300 MHz, CDCl3) δ 1.18 (s, 3H, CH3), 1.62 (s, 3H, CH3), 2.63 and 2.79 (AA’, H74 J = 19.2 Hz), 3.03 (s, 1H, H2), 3.84 (s, 3H, OCH3), 6.99–7.39 (m, 9H, Harom). 13C NMR (CDCl3; 75.47 MHz) δ 20.8 and 20.9 (CH3), 31.3 (C4), 31.8 (C1), 34.0 (C3), 40.2 (C2), 55.6 (OCH3), 114.5–159.4 (Carom), 175.6 (C6) 200.8 (C7). HRMS (ESI) Calcd for C21H21NO3 335.1521 [M+]. Found: 335.1516. Elemental analysis: C21H21NO3 requires C, 75.20; H, 6.31; N, 4.18%; found C, C, 75.17; H, 6.28; N, 4.17%.

4.4.4. 2,5-bis(4-Methoxyphenyl)-1,1-Dimethyl-5-Azaspiro[2.4]heptane-6,7-Dione (5d)

Yield (70%), white solid. Mp = 163–164 °C, Rf = 0.29 (cyclohexane/EtOAc 3:7). 1H NMR (300 MHz, CDCl3) δ 1.17 (s, 3H, CH3), 1.61 (s, 3H, CH3), 2.61 and 2.76 (AA’, H74 J = 19.2 Hz), 2.95 (s, 1H, H2), 3.81 (s, 3H, OCH3), 3.84 (s, 3H, OCH3), 6.87–8.04 (m, 8H, Harom). 13C NMR (CDCl3; 75.47 MHz) δ 20.7 and 20.9 (CH3), 31.3 (C4), 31.9 (C1), 34.0 (C3), 39.7 (C2), 55.4 (OCH3), 55.6 (OCH3), 113.8–159.4 (Carom), 175.6 (C6) 200.9 (C7). HRMS (ESI) Calcd for C22H23NO4 365.1627 [M+]. Found: 365.1630. Elemental analysis: C22H23NO4 requires C, 72.31; H, 6.34; N, 3.83%; found C, 72.29; H, 6.31; N, 3.81%.

4.5. Study of the Insecticidal Activity of Spiro-Cyclopropane , the Trans-Chrysanthemic Acid and Pyrethrin

Biological laboratory tests have been carried out to screen new products for their effectiveness against mosquitoes (Aedes aegypti) and house flies (Musca domestica). Detailed rearing procedures for each insect are provided in the Supplementary Material.

4.5.1. Effects of Cyclopropanes 5a–d at Contact Action against Aedes aegypti

The mosquitoes were obtained in the egg state and subsequently stored at a temperature of 30 °C and relative humidity of 47%. Each test was performed in a test tube and was repeated 3 times. Acetone was used as the dilution solvent. The spiro-cyclopropanes 5a–d, the trans-chrysanthemic acid and pyrethrin were dissolved in acetone at different concentrations (C = 0.001, 0.005 and 0.01%). The sheets of cellulose paper were immersed with the solutions prepared at the rate of 0.12 μL of mm−2 solution and then dried and placed in the test tubes. The tests were carried out with ten female mosquitoes aged 1 to 3 days. The mosquitoes were released inside the tube, and then the cap was closed. Knockdown of Aedes aegypti was observed at the indicated intervals up to 60 min. Subsequently, the mosquitoes were placed in untreated glass (250 mL) containing cotton soaked in firm sugar water. Rollover and mortality were observed for 24 h (Table 1).

4.5.2. Effects of Cyclopropanes 5a–d in the Vapor Phase against Aedes aegypti

This test was carried out in a stainless-steel enclosure with three doors, with a volume of 22.5 m3 and the following dimensions: length 3 m; width 3 m; height 2.5 m. The temperature inside the chamber was maintained at 21–25 °C and the relative humidity at 50–60%. The mosquitoes were introduced into mesh polyester cages of dimensions: length 8 cm, diameter 8 cm and mesh 2 mm. Then, they were suspended from the ceiling of the stainless-steel enclosure at a height of 1.5 and 0.5 m from the walls (see Figure 1). The insecticidal effect was studied by keeping 20 mixed-sex mosquitoes for 3 days in each wire cage. Cellulose papers (10 × 10 cm) immersed in a solution of each cyclopropane, trans-chrysanthemic acid and pyrethrin (5 mg) were placed above the fans for 8 h. Let T10, T50 and T90 represent the times required to kill 10, 50 and 90% of mosquitoes, respectively. Results were recorded every 2 h. The insects were removed from the cages after 12 h and transferred to glasses (250 mL) provided with cellulose pads soaked in a 10% sugar solution. Mortality was recorded 24 h after treatment (Table 2).

4.5.3. Aerosols Effects of Cyclopropanes 5a–d Liquid Formulation against Aedes aegypti and Musca Domestica

This test was carried out in a stainless-steel enclosure with three doors, with a volume of 22.5 m3 and the following dimensions: length 3 m; width 3 m; height 2.5 m. The temperature inside the chamber was maintained at 21–25 °C and the relative humidity at 50–60%. The mosquitoes were introduced into mesh polyester cages (length 8 cm, diameter 8 cm, mesh 2 mm) and were suspended from the ceiling of the stainless-steel enclosure at a height of 1.5 and 0.5 m from the walls. The prepared solution was sprayed vertically at a height of 1 m in the center of the enceinte. A fan placed on the floor operated for 5 min. The times T10, T50 and T90 were recorded every 2 h. The insects were removed from the cages after 12 h and transferred to glasses (250 mL) provided with cellulose pads soaked in a 10% sugar solution. Mortality was recorded 24 h after treatment (Table 3 and Table 4).

4.6. Docking

4.6.1. Preparation of Cyclopropanes 5a–d and Trans-Chrysanthemic Acid for Docking Analysis

All these molecular structures were reproduced in Chem-drawn ultra-version, and then all ligands were saved in mol format, with the aim of opening these files in MOE after structure preparation, and these were protonated 3D with energy minimized through MOE using default parameters.

4.6.2. Preparation of Protein and Molecular Docking

The crystal structure of the protein (PDB: 5FT3) was obtained from the RSCB data bank (https://www.rcsb.org, accessed on 8 January 2021). The protein was prepared by removing the complexed inhibitor ligand and water molecules. Then, the polar hydrogens were added, followed by appending Kollman charges. Hence, the grid box with dimensions of 40 × 40 × 40 points, spacing of 1.0 Å and centered with coordinates x: −11.993, y: 15.425, and z: 65.951, was generated based on the N3 binding position in the target protein binding site. While performing docking, the ligand atom was selected, and rescoring1 was set at London dG and rescoring2 at GBVI/WSA dG, running to note the ligand interaction with protein. Protein–ligand docking score, ligand properties and 2D and 3D structures were saved. The docking calculations have been carried out using an Intel (R) Core (TM) CPU @ 3.4 GHz Workstation.