Facial Regioselective Synthesis of Novel Bioactive Spiropyrrolidine/Pyrrolizine-Oxindole Derivatives via a Three Components Reaction as Potential Antimicrobial Agents

Abstract

This article presents the synthesis of new derivatives of spirooxindole-spiropiperidinone- pyrrolidines 6a–j and spirooxindole-spiropiperidinone-pyrrolizines 8a–j, through a 1,3-dipolar cycloaddition reaction of azomethineylides generated from isatin, sarcosine, and l-proline, through a decarboxylative route with dipolarophile 4a–j. All of the newly synthesized compounds were evaluated for their antimicrobial activities and their minimum inhibitory concentration (MIC) against most of the test organisms. The tested compounds displayed excellent activity against all of the tested microorganisms.

1. Introduction

In recent years, multicomponent reactions (MCR’s) [1,2,3] leading to interesting heterocyclic scaffolds have emerged as powerful tools for the diverse needs in combinatorial approaches for the synthesis of bioactive compounds, creating distinct chemical libraries of drug-like molecules for biological screening [4,5]. Spiro compounds represent an important class of naturally occurring substances with highly pronounced biological properties [6,7]. Spirooxindole ring systems are found in a number of alkaloids, such as horsifiline, spirotryprostain, and (+) elacomine [8], and are used in biological applications as antimicrobial and antitumor agents and as inhibitors of the human NKI receptor [9]. Additionally, spirooxindole rings containing the pyrrolidine and pyrrolizine ring system are found in various natural products as fundamental nuclei and are well recognized for exhibiting a wide range of pharmacological and biochemical behaviors [10,11,12]. The 1,3-cycloaddition methodology is one of the simplest tools for the construction of five-membered heterocycles. The ease of generating a 1,3-dipolar, coupled with the observed highly regio- and stereoselective nature of cycloaddition, has led to a number of syntheses that utilize such a reaction [13]. Combining several transformations into a one-pot reaction has proved to be an excellent strategy for increasing the efficiency of organic synthesis [14]. In particular, azomethineylides have been used to synthesize pyrrolidines and pyrrolizines with various substitutions, allowing the introduction of several functional groups in a single operation [15]. As part of our own interest in the synthesis of biologically active heterocyclic compounds [16,17,18,19,20,21,22,23], we report an efficient methodology for the synthesis of novel spirooxindole-spiropiperidinone-pyrrolidine and spirooxindole-spiropiperidinone-pyrrolizine derivatives, and investigate their antimicrobial activities.

2. Results and Discussion

2.1. Chemistry

In our initial endeavor, the Knoevenagel adduct 4 was prepared via condensation of 1-ethoxycarbonyl-4-piperidinone with aromatic aldehydes, in the presence of a base catalyst [24]. Then, the three-component reaction of isatin 1, sarcosine 2, and ethyl 3,5-bis[phenylmethylidene]-4-oxopiperidine-N-carboxylate 4a, as a simple model substrate, was investigated, to establish the feasibility of the strategy and optimize the reaction conditions. The reaction was carried out at 60 °C in methanol and took around 120 min. It was then cooled to room temperature and the solid that formed was filtered and recrystallized from methanol to furnish the functional dispiropyrrolidinyloxindole in a highly regioselective manner, to afford 6a (Scheme 1).

The dispiroheterocyclic ring structure of products 6a–j was confirmed by spectroscopic data (IR, ¹H- and ¹³C-NMR) and elemental analysis. The IR spectrum of 6a revealed the presence of a carbonyl stretching vibration band at 1685 cm⁻¹, showing an increase of 18 cm⁻¹ from the normal value observed for 3,5-bis[phenylmethylidene]-4-oxipiperidine-N-carboxylate 4a, indicating the loss of conjugation from one side. It also exhibited two bands at 1718 and 1710 cm⁻¹, due to the carbonyl group of oxindole and ester moiety, respectively. On the other hand, the ¹H-NMR spectrum of 6a showed a sharp singlet signal at δ 1.98 for thepyrroline-N-CH₃ proton. The benzylic proton H_a exhibited a doublet of the doublet in the region δ 4.82, with (J = 10.7, 9.0 Hz). The H_c and H_b protons appeared as a doublet of the doublet in the region δ 3.91 with (J = 10.7, 7.0 Hz) and 3.43 with (J = 9.0, 7.0 Hz), respectively. The protons of the piperidinone ring appeared as a multiple signal in the region δ 3.32–3.39. Also, the olefinic proton was observed at δ 7.59 as a singlet, whereas the aromatic protons appeared as multiplets in the region δ 6.75–7.47, and as a broad singlet at δ 8.56 for the NH proton of the oxindole ring.

The regiochemistry of the product 6a was confirmed by the ¹H-NMR spectra. The benzylic proton H_a was observed at δ 4.82, as a doublet of the doublet. If the other isomer was formed, one would expect a singlet, instead of a doublet of the doublet, for this benzylic proton. The ¹³C-NMR spectra of 6a exhibited peaks at δ 64.2 ppm and 76.2 ppm for two spiro carbons. The peaks at δ 154.32, δ 173.2, and at δ 202.12 ppm, were due to the ester carbonyl, oxindole carbonyl, and keto carbonyl carbons of the N-COOEt piperidinone ring system, respectively. The mass spectra of 6a showed a molecular ion peak at m/z 521 (M⁺), which further confirmed the formation of a mono-adduct.

After the formation of the mono-adduct, the reaction failed to give the bis-adduct, even with an excess of 1,3-dipole and a prolonged reaction time. This may be due to the steric hindrance and fixing of the geometry of the spiropyrrolidine ring, which prevents afurther attack of 1,3-dipole on the other exocyclic double bond. However, bis-adducts are formed if a small 1,3-dipole is generated [25].

This reaction proceeds through the decarboxylative condensation of isatin 1 with sarcosine 2, to generate an azomethineylide 3. The generated 1,3-dipole cycloaddition with the dipolarophile 4a–j produces novel dispiro-oxindolopyrrolidines 6a–j (Scheme 1).

To enhance the yield, endeavors were made to streamline other response parameters, including the solvents and reaction temperature. Thus, the reaction was studied in different solvents that included THF, toluene, CH₃CN, CH₃OH, EtOH, and H₂O (

Table 1. Optimization of reaction condition.

Entry	Solvent	Temp (°C)	Yield a (%)
1	THF	60	54
2	Toluene	60	trace
3	CH3CN	60	72
4	CH3OH	60	92
5	EtOH	60	85
6	Water	60	NR
7	CH3OH	30	58
8	CH3OH	45	66

^a isolated yield based on isatin.

, entries 1–6). To our satisfaction, the reaction in methanol led to the desired product with an almost quantitative yield (92%) (Table 1, entry 4), while ethanol as a solvent produced the product with only an 85% yield (Table 1, entry 5). In general, the reactions carried out in protic solvents yielded better results than those in aprotic solvents. However, when water was employed as the solvent, no product was detected (Table 1, entry 6). This might be caused by the poor solubility of isatin 1 and ethyl 3,5-bis[phenylmethylidene]-4-oxopiperidine-N-carboxylate 4a–j in water.

The temperature influenced the rate of the reaction. Reducing the reaction temperature resulted in low reactivity (Table 1, entries 7 and 8), while elevating the temperature to 60 °C provided the best results. Based on the comprehensive consideration of the reaction temperature and yield, the optimal reaction conditions were established, as shown in Table 1 entry 4.

Considering the optimized conditions, the 1,3-dipolar cycloaddition reaction of Knoevenagel adducts with different structures, was investigated. As shown in

Table 2. Yields of spiropyrrolidine and spiropyrrolizinebisoxindoles.

Entry	Ar	6 & 8	Yield a (%)
1	C6H5	6a	92
2	4-NO2C6H4	6b	95
3	4-ClC6H4	6c	91
4	4-FC6H4	6d	92
5	4-OCH3C6H4	6e	84
6	3,4-Cl2C6H3	6f	87
7	2,4-F2C6H3	6g	89
8	3,4-OCH3·C6H3	6h	79
9	4-F3CC6H4	6i	86
10	3,4,5-OCH3 C6H2	6j	81
11	C6H5	8a	90
12	4-NO2C6H4	8b	88
13	4-ClC6H4	8c	82
14	4-FC6H4	8d	85
15	4-OCH3C6H4	8e	80
16	3,4-Cl2C6H3	8f	82
17	2,4-F2C6H3	8g	83
18	3,4-OCH3·C6H3	8h	81
19	4-F3CC6H4	8i	79
20	3,4,5-OCH3 C6H2	8j	87

^a isolated yield based on isatin.

, a variety of Knoevenagel adducts proved to be excellent dipolarophiles for this reaction and provided the corresponding spiropyrrolidine bisoxindoles with good yields (up to 95%) (Table 2, entries 1–10).

Substituents on the aryl groups lightly influenced the yields. Generally, Knoevenagel adducts with electron-donating groups produced lower yields than those with electron-withdrawing groups (Table 2).

On the basis of the above mentioned results, we extended our protocol to the synthesis of dispiro-oxindolopyrrolizines 8a–j from isatin 1, aminoacid 7 such as l-proline, and ethyl 3,5-bis[arylmethylidene]-4-oxipiperidine-N-carboxylate 4a–j in methanol, to yield a single product, as evidenced by TLC and spectral analysis (Scheme 2).

For example, in the ¹H-NMR spectra of 8a, the H_a appears as a doublet at δ 3.26 ppm (J = 10.2 Hz) and multiplet of H_b at δ 2.51–2.55 ppm. The singlet at δ 8.53 ppm is due to the NH of the oxindole ring. The ¹³C-NMR spectra of 8a exhibited peaks at δ 62.1 ppm and 71.4 ppm for two spiro carbons. The peaks at δ 154.5, δ 173.2, and δ 199.2 ppm were due to the ester carbonyl, oxindole carbonyl, and keto carbonyl carbons of the N-COOEt piperidinone ring system, respectively. The mass spectra of 8a showed a molecular ion peak at m/z 547 (M⁺), which further confirmed the formation of a mono-adduct.

Several advantages, such as a high yield, and simple experimental and isolation procedures, render the methanol an efficient route for the synthesis of spiro-frameworks from isatin, sarcosine, and l-proline, that are important compounds in organic and medicinal chemistry.

2.2. Antimicrobial Activity

The in vitro antimicrobial screening of compounds prepared in this study was carried out using the cultures of four bacteria species, namely, the Gram positive bacteria, Streptococcus pneumonia (RCMB 010010) (SP) and Bacillis subtilis (RCMB 010067) (BS), and the Gram negative bacteria, Pseudomonas aeruginosa (RCMB 010043) (PS), and Escherichia coli (RCMB 010052) (EC); as well as four fungal strains, including Aspergillus fumigates (RCMB 02568) (AF), Syncephalastrumracemosum (RCMB 05922) (SR), Geotricumcandidum (RCMB 05097) (GC), and Candida albicans (RCMB05036) (CA). Amphotericin B as an antifungal agent, Ampicillin as an antibacterial agent for gram (+) bacteria, and Gentamicin as an antibacterial agent for gram (−) bacteria, were used as references to evaluate the potency of the tested compounds under the same conditions. Most of the newly synthesized compounds showed excellent results with respect to the control drugs. The results of antimicrobial activities are shown in

Table 3. Antimicrobial activity of the synthesized compounds.

Compd. No.	Gram Positive Bacteria		Gram Negative Bacteria		Fungi
	S. pneumoniae	B. subtilis	P. aeruginosa	E. coli	A. fumigatus	S. racemosum	G. candidum	C. albicans
6b	42.34 ± 0.15	74.25 ± 0.42	NA	49.25 ± 0.53	42.36 ± 0.33	49.32 ± 0.25	63.25 ± 0.34	NA
6c	96.25 ± 0.2	97.24 ± 0.3	49.25 ± 0.1	74.29 ± 0.3	96.25 ± 0.1	74.25 ± 0.2	95.36 ± 0.2	91.29± 0.1
6e	53.21 ± 0.43	63.28 ± 0.53	NA	24.29 ± 0.25	53.24 ± 0.58	63.29 ± 0.25	74.16 ± 0.38	NA
6g	49.21 ± 0.44	53.21 ± 0.67	NA	21.34 ± 0.46	25.36 ± 0.25	49.24 ± 0.34	49.24 ± 0.58	NA
6i	74.12 ± 0.63	74.95 ± 0.32	NA	42.34 ± 0.46	53.21 ± 0.36	63.24 ± 0.44	78.21 ± 0.58	NA
6j	63.24 ± 0.63	74.21 ± 0.32	NA	34.25 ± 0.46	42.15 ± 0.36	49.21 ± 0.44	53.21 ± 0.58	NA
8b	74.52 ± 0.44	91.25 ± 0.63	NA	49.25 ± 0.25	74.32 ± 0.39	82.63 ± 0.16	90.33 ± 0.58	NA
8c	34.25 ± 0.44	42.67 ± 0.25	NA	22.14 ± 0.33	39.25 ± 0.25	39.46 ± 0.58	42.67 ± 0.17	NA
8e	78.26 ± 0.34	96.25 ± 0.25	NA	49.25 ± 0.58	74.25 ± 0.63	78.23 ± 0.27	82.34 ± 0.35	NA
8g	95.44 ± 0.44	95.34 ± 0.58	22.14 ± 0.58	74.21 ± 0.19	53.22 ± 0.34	74.25 ± 0.25	92.68 ± 0.58	NA
8i	74.25 ± 0.44	96.25 ± 0.63	NA	34.24 ± 0.25	74.25 ± 0.39	49.25 ± 0.58	78.34 ± 0.58	NA
8j	74.65 ± 0.43	78.34 ± 0.53	NA	42.37 ± 0.33	82.65 ± 0.25	78.34 ± 0.25	98.25 ± 0.38	NA
Ampicillin	96.25 ± 0.2	97.24 ± 0.3	NA	NA	NA	NA	NA	NA
Gentamicin	NA	NA	49.25±0.1	74.29 ± 0.3	NA	NA	NA	NA
Amphotericin B	NA	NA	NA	NA	96.25 ± 0.1	74.25 ± 0.2	95.36 ± 0.2	91.29 ± 0.1

NA: No activity.

. The data in Table 3 revealed that most of the compounds have a superior and significant antibacterial potency to antifungal activity. It is clear from the data in Table 3 that compounds 8b, 8e, 8g and 6c exhibited the highest potency against tested organisms, with respect to the reference drugs. The other derivatives showed moderate activity against the microorganisms used. The compounds 6c and 8g exhibited antimicrobial activity against all of the tested microorganisms. It has also been observed that the newly synthesized compounds exhibited more promising antibacterial activity against Gram positive bacteria than Gram negative bacteria, displaying the highest activity against Bacillis subtilis (RCMB 010067).

The minimum inhibitory concentration (MIC) of the most active synthesized compounds against highly inhibited organisms, is reported in

Table 4. Antimicrobial Activity as MICS (µg/mL) of tested samples against tested microorganisms.

Compd. No.	Gram Positive Bacteria		Gram Negative Bacteria		Fungi
	S. pneumoniae	B. subtilis	P. aeruginosa	E. coli	A. fumigatus	S. racemosum	G. candidum	C. albicans
6c	0.12	0.015	15.63	1.95	0.015	1.95	0.015	0.06
8b	1.95	0.06	NA	15.63	1.95	0.49	0.12	NA
8e	0.98	0.015	NA	15.63	1.95	0.98	0.49	NA
8g	0.015	0.015	NA	1.95	7.81	1.95	0.03	NA
Amphotericin B	NA	NA	NA	NA	0.015	1.95	0.015	0.06
Ampicillin	0.015	0.007	NA	NA	NA	NA	NA	NA
Gentamicin	NA	NA	15.63	1.95	NA	NA	NA	NA

NA: No activity.

. Compounds 8b, 8e, 8g and 6c revealed the lowest MICs (0.06, 0.015, 0.015, and 0.015 µg/mL) against Bacillis subtilis (RCMB 010067), respectively.

The inhibitory concentration of the most active synthesized compounds against 50% of microorganism growth (IC₅₀), is reported in

Table 5. Antimicrobial Activity as IC₅₀ (µg/mL) of tested samples against tested microorganisms.

Compd. No.	Gram Positive Bacteria		Gram Negative Bacteria		Fungi
	S. pneumoniae	B. subtilis	P. aeruginosa	E. coli	A. fumigatus	S. racemosum	G. candidum	C. albicans
6c	3.98	1.34	36.25	17.63	1.96	16.37	1.45	2.16
8b	16.35	2.92	NA	32.84	18.36	10.64	4.29	NA
8e	12.36	1.36	NA	32.12	16.32	11.32	9.25	NA
8g	1.73	1.24	>125	15.98	21.36	16.38	2.09	NA
Amphotericin B	NA	NA	NA	NA	1.25	14.27	1.16	2.48
Ampicillin	1.53	1.06	NA	NA	NA	NA	NA	NA
Gentamicin	NA	NA	20.31	16.62	NA	NA	NA	NA

NA: No activity.

. Compounds 8b, 8e, 8g and 6c revealed the lowest IC₅₀ values (2.92, 1.34, 1.36, and 1.24 µg/mL) against Bacillis subtilis (RCMB 010067), respectively.

Then, a study of the structure-activity relationships (SAR) showed that 8 compounds with a phenyl-hexahydro-1H-pyrrolizine ring, were more capable of improving the antimicrobial activity than compounds 6 with (-CH₃) a pyrrolidine ring.

According to the antimicrobial data, we evaluated the effect of introducing different substituent group(s) at phenyl rings in synthesized compounds. The introduction of electron-withdrawing groups (halogen groups or -NO₂) showed better antimicrobial effects than the electron-donating group (4-OCH₃, 3,4,5-(OCH₃)₃).

3. Experimental Section

3.1. General Procedures

Melting points were determined using a Gallenkamp electro-thermal apparatus and wereuncorrected. IR spectra were recorded as KBr disc, using a Shimadzu FTIR-prestige 21 spectrophotometer. ¹H- and ¹³C-NMR spectra were recorded in DMSO-d₆ as solvents (at 300 MHz for ¹H and 75 MHz for ¹³C) on a Varian Mercury NMR spectrometer, using TMS as the internal standard. Chemical shifts δ are reported in parts per million units (ppm), and J values are given in hertz. The mass spectra were recorded on a GCeMS-QP1000 EX mass spectrometer at 70 eV. Elemental analyzes were measured using a German made elementary vario LIII CHNS analyzer. Antibacterial activity was studied at the Regional Center for Mycology and Biotechnology at Al-Azhar University, Cairo, Egypt. Compounds 4a–c, 4e and 4h were prepared as previously reported in the respective literature [24].

3.2. General Procedure for the Preparation of 3,5-bis[Arylmethylidene]-4-oxopiperidine-N-carboxylate (4d,f,g,i,j)

A mixture of 1-ethoxycarbonyl-4-piperidinone (1.71 mL, 10 mmol) and aromatic aldehydes (20 mmol) in methanol (20 mL), in the presence of potassium hydroxide, was used as the base catalyst (1 g). The mixture was stirred at room temperature for 30 min. The solid formed was collected, washed with methanol, and crystallized from proper solvent, to give the compounds, as listed below:

Ethyl 3,5-bis[4-fluorophenyl-methylidene]-4-oxopiperidine-N-carboxylate (4d). Yellow solid, m.p. 210–212 °C (EtOH); IR (KBr): 1717, 1687 (2CO) cm⁻¹. ¹H-NMR (DMSO-d₆); 1.12 (t, 3H, J = 7.2 Hz, CH₃ of CH₂CH₃), 3.92 (s, 4H, 2CH₂ of piperidinone), 4.75 (q, 2H, J = 7.2 Hz, CH₂ of CH₂CH₃), 7.40–7.55 (m, 8H, Ar-H), 7.67 (s, 2H, 2CH=). ¹³C-NMR (DMSO-d₆); 13.2, 59.5, 45.5, 117.0, 128.2, 133.2, 142.3, 145.9, 164.2, 155.3, 185.1. MS m/z (%): 385 (M⁺ + 2, 40), 384 (M⁺ + 1, 23), 383 (M⁺, 45), 206 (14), 97 (30), 57 (15). Anal. for C₂₂H₁₉F₂NO₃ (383.39): calcd. C, 68.92; H, 5.0; N, 3.65. Found C, 68.65; H, 5.10; N, 3.54.

Ethyl 3,5-bis[3,4-dichlorophenyl-methylidene]-4-oxopiperidine-N-carboxylate (4f). Yellow solid, m.p. 208–210 °C (EtOH/Dioxane); IR (KBr): 1720, 1688 (2CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.13 (t, 3H, J = 7 Hz, CH₃ of CH₂CH₃), 3.93 (s, 4H, 2CH₂ of piperidinone), 4.73 (q, 2H, J = 7 Hz, CH₂ of CH₂CH₃), 7.45–7.56 (m, 6H, Ar-H), 7.66 (s, 2H, 2CH=). MS m/z (%): 487 (M⁺ + 2, 50), 486 (M⁺ + 1, 30), 485 (M⁺, 32), 167 (15), 147 (10). Anal. For C₂₂H₁₇Cl₄NO₃ (485.18): calcd. C, 54.46; H, 3.54; N, 2.89. Found: C, 54.45; H, 3.82; N, 2.63.

Ethyl 3,5-bis[2,4-difluorophenyl-methylidene]-4-oxopiperidine-N-carboxylate (4g). Yellow solid, m.p. 167–168 °C (EtOH/Dioxane); IR (KBr): 1715, 1686 (2CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.2 (t, 3H, J = 7.2 Hz, CH₃ of CH₂CH₃), 3.91 (s, 4H, 2CH₂ of piperidinone), 4.56 (q, 2H, J = 7.2 Hz, CH₂ of CH₂CH₃), 7.53–7.76 (m, 6H, Ar-H), 7.84 (s, 2H, 2CH=). ¹³C-NMR (DMSO-d₆): δ 14.22, 59.3, 46.7, 105, 112.2, 119.2, 130.4, 140.2, 145.9, 154.7, 160.3, 165.1, 185.8. MS m/z (%): 421 (M⁺ + 2, 5), 420 (M⁺ + 1, 23), 419 (M⁺, 42), 206 (12), 97 (10), 57 (9). Anal. for C₂₂H₁₇F₄NO₃ (419.38): calcd. C, 63.00; H, 4.27; N, 3.62. Found: C, 63.11; H, 4.26; N, 3.42.

Ethyl 3,5-bis[4-trifluoromethylphenyl-methylidene]-4-oxo-piperidine-N-carboxylate (4i). Yellow solid, m.p. 147–149 °C (EtOH/Dioxane); IR (KBr): 1709, 1691 (2CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.19 (t, 3H, J = 7.1 Hz, CH₃ of CH₂CH₃), 3.86 (s, 4H, 2CH₂ of piperidinone), 4.24 (q, 2H, J = 7.1 Hz, CH₂ of CH₂CH₃), 7.21–7.53 (m, 8H, Ar-H), 7.83 (s, 2H, 2CH=). MS m/z (%): 485 (M⁺ + 2, 25), 484 (M⁺ + 1, 38), 483 (M⁺, 62), 158 (23), 145 (20). Anal. for C₂₄H₁₉F₆NO₃ (483.41): calcd. C, 59.63; H, 3.96; N, 2.90. Found: C, 59.91; H, 4.00; N, 2.71.

Ethyl 3,5-bis[3,4,5-trimethoxyphenyl-methylidene]-4-oxopiperidine-N-carboxylate (4j). Yellow solid, m.p. 126–127 °C (EtOH); IR (KBr): 1718, 1686 (2CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.2 (t, 3H, J = 7.2 Hz, CH₃ of CH₂CH₃), 2.49 (s, 4H, 2CH₂ of piperidinone), 3.17 (s, 6H, CH₃ of OCH₃), 3.65 (s, 6H, CH₃ of OCH₃), 3.72 (s, 6H, CH₃ of OCH₃), 4.8 (q, 2H, J = 7.2 Hz, CH₂ of CH₂CH₃), 6.84 (s, 4H, Ar-H), 7.24 (s, 2H, 2CH=). ¹³C-NMR (DMSO-d₆): δ 13.6, 58.9, 46.4, 56.1, 56.5, 105, 129.2, 140.1, 151.2, 140.5, 145.7, 154.9, 186.7. MS m/z (%): 529 (M⁺ + 2, 6), 528 (M⁺ + 1, 20), 527 (M⁺, 63), 97 (15), 57 (9). Anal. for C₂₈H₃₃NO₉ (527.57): calcd. C, 63.75; H, 6.31; N, 2.66. Found: C, 63.50; H, 6.41; N, 2.69.

3.3. General Synthesis of Dispiropyrrolidine Oxindole Derivatives (6a–j)

A reaction mixture of isatin 1 (1.47 g, 10 mmol), sarcosine 2 (0.89 g, 10 mmol), and Ethyl 3,5-bis(arylmethylidene)-N-carboxyl-4-piperidinone 4a–j (10 mmol), was produced by refluxing it in methanol for 120 min at 60 °C, and was then poured on water. The solid formed was collected and crystallized from a suitable solvent to produce white to brown crystals of compounds (6a–j).

Ethyl 1-N-methyl-spiro[2.3′]oxindole-spiro[3.3′′]5′′-benzylidene-1′′-N-carboxylate-4′′-piperidinone-4-phenyl-pyrrolidine (6a). White crystals, m.p. 160–162 °C (EtOH/Dioxane); IR (KBr): 3253 (NH), 1718, 1710, 1685 (3CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.15 (t, 3H, J = 7.2 Hz, CH₃ of CH₂CH₃), 1.98 (s, 3H, NCH₃), 3.32, 3.39 (2s, 4H, 2CH₂ of piperidinone ring), 3.43 (dd, J = 9.0, 7.0 Hz, 1H_b), 3.91 (dd, J = 10.7, 7.0 Hz, 1H_c), 4.39 (q, 2H, J = 7.2 Hz, CH₂ of CH₂CH₃), 4.82 (dd, J = 10.7, 9.0 Hz, 1H_a), 6.75–7.47 (m, 14H, Ar-H), 7.59 (s, 1H, CH=), 8.56 (s, 1H, D₂O-exchangeable, NH). ¹³C-NMR (DMSO-d₆): δ 13.7, 29.9, 38.1, 43.2, 46.7, 55.3, 59.3, 64.2, 76.2, 121.6, 124.1, 126.3, 126.4, 126.5, 127.4, 127.9, 128.2, 128.5, 136.2, 136.4, 138.2, 139.5, 141.2, 153.9, 154.3, 173.2, 202.1. MS m/z (%): 523 (M⁺ + 2, 9), 522 (M⁺ + 1, 25), 521 (M⁺, 35), 130 (14), 77 (30). Anal. for C₃₂H₃₁N₃O₄ (521.62): calcd. C, 73.68; H, 5.99; N, 8.06.Found C, 73.53; H, 5.94; N, 8.02.

Ethyl 1-N-methyl-spiro[2.3′]oxindole-spiro[3.3′′]5′′-(4-nitro)benzylisdene-1′′-N-carboxylate-4′′-piperidinone-4-(4-nitro)phenyl-pyrrolidine (6b). Yellow crystals, m.p. 175–176 °C (Dioxane); IR (KBr): 3262 (NH), 1714, 1701, 1692(3CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.18 (t, 3H, J = 7 Hz, CH₃ of CH₂CH₃), 2.03 (s, 3H, NCH₃), 3.22 (dd, J = 9.0, 7.0 Hz, 1H_b), 3.30, 3.45 (2s, 4H, 2CH₂ of piperidinone ring), 3.84 (dd, J = 10.7, 7.0 Hz, 1H_c), 4.18 (q, 2H, J = 7 Hz, CH₂ of CH₂CH₃), 4.79 (dd, J = 10.7, 9.0 Hz, 1H_a), 6.76–7.82 (m, 12H, Ar-H), 8.40 (s, 1H, CH=), 11.01 (s, 1H, D₂O-exchangeable, NH). ¹³C-NMR (DMSO-d₆): δ 13.5, 29.9, 37.8, 43.5, 46.9, 55.8, 58.9, 64.3, 76.5, 121.6, 124.1, 126.1, 126.4, 126.6, 127.1, 127.4, 128.6, 128.8, 128.9, 136.2 , 136.3, 138.2, 139.5, 141.5, 153.9, 158.3, 175.2, 201.5. MS m/z (%): 613 (M⁺ + 2, 8), 612 (M⁺ + 1, 35), 611 (M⁺, 98), 242 (12), 205 (15), 97 (15). Anal. For C₃₂H₂₉N₅O₈ (611.61): calcd. C, 62.84; H, 4.78; N, 11.45. Found: C, 62.78; H, 4.69; N, 11.36.

Ethyl 1-N-methyl-spiro[2.3′]oxindole-spiro[3.3′′]5′′-(4-chloro)benzylidene-1′′-N-carboxylate-4′′-piperidinone-4-(4-chloro)phenyl-pyrrolidine (6c). Yellow crystals, m.p. 185–187 °C (EtOH/Dioxane); IR (KBr): 3251 (NH), 1716, 1708, 1686 (3CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.16 (t, 3H, J = 7.2 Hz, CH₃ of CH₂CH₃), 1.97 (s, 3H, NCH₃), 3.11 (dd, J = 9.0, 7.0 Hz, 1H_b), 3.29, 3.38 (2s, 4H, 2CH₂ of piperidinone ring), 3.89 (dd, J = 10.7, 7.0 Hz, 1H_c), 4.20 (q, 2H, J = 7.2 Hz, CH₂ of CH₂CH₃), 4.72 (dd, J = 10.7, 9.0 Hz, 1H_a), 6.72–7.49 (m, 12H, Ar-H), 7.56 (s, 1H, CH=), 10.48 (s, 1H, D₂O-exchangeable, NH). ¹³C-NMR (DMSO-d₆): δ 13.8, 29.8, 37.8, 43.2, 46.6, 55.5, 59.1, 63.9, 76.1, 121.2, 124.1, 126.4, 127.2,128.4, 128.6, 128.8, 130.1, 131.1, 133.4, 133.8, 136.6 , 137.6, 139.3, 139.7, 152.6, 154.0, 172.3, 203.9. MS m/z (%): 592 (M⁺ + 2, 6), 591 (M⁺ + 1, 34), 590 (M⁺, 88), 242 (12), 97 (15). Anal. For C₃₂H₂₉Cl₂N₃O₄ (589.50): calcd. C, 65.09; H, 4.95; N, 7.12.Found C, 65.01; H, 4.86; N, 7.06.

Ethyl 1-N-methyl-spiro[2.3′]oxindole-spiro[3.3′′]5′′-(4-fluoro) benzylidene-1′′-N-carboxylate-4′′-piperidinone-4-(4-fluoro)phenyl-pyrrolidine (6d). Brown crystals, m.p. 215–217 °C (Dioxane); IR (KBr): 3256 (NH), 1720, 1711, 1684 (3CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.19 (t, 3H, J = 7.4 Hz, CH₃ of CH₂CH₃), 2.18 (s, 3H, NCH₃), 3.17 (dd, J = 9.0, 7.0 Hz, 1H_b), 3.36, 3.48 (2s, 4H, 2CH₂of piperidinone ring), 3.86 (dd, J = 10.5, 7.0 Hz, 1H_c), 4.19 (q, 2H, J = 7.4 Hz, CH₂ of CH₂CH₃), 4.71 (dd, J = 10.5, 9.0 Hz, 1H_a), 6.75–7.33 (m, 12H, Ar-H), 7.40 (s, 1H, CH=), 10.5 (s, 1H, D₂O-exchangeable, NH).¹³C-NMR (DMSO-d₆): δ 13.5, 29.7, 37.9, 42.9, 46.6, 54.7, 59.1, 63.7, 76.1, 114.7 ,115.3, 121.4, 124.3, 126.2, 128.1, 128.5, 130.2, 130.9, 136.4, 136.7, 137.9, 139.5, 159.8, 162.2, 152.6, 154.4, 173.4, 201.6. MS m/z (%): 559 (M⁺ + 2, 3), 558 (M⁺ + 1, 35), 557 (M⁺, 85), 206 (10), 97 (8). Anal for C₃₂H₂₉F₂N₃O₄ (557.60): calcd. C, 68.93; H, 5.24; N, 7.54.Found C, 68.87; H, 5.21; N, 7.49.

Ethyl 1-N-methyl-spiro[2.3′]oxindole-spiro[3.3′′]5′′-(4-methoxy) benzylidene-1′′-N-carboxylate-4′′-piperidinone-4-(4-methoxy)phenyl-pyrrolidine (6e). Yellow crystals, m.p. 118–120 °C (Methanol); IR (cm⁻¹): 3251 (NH), 1716, 1702, 1674 (3CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.13 (t, 3H, J = 7.2 Hz, CH₃ of CH₂CH₃), 2.09 (s, 3H, NCH₃), 3.25 (dd, J = 9.0, 7.0 Hz, 1H_b), 3.33, 3.49 (2s, 4H, 2CH₂ of piperidinone ring), 3.85, 3.87 (2s, 6H, 2OCH₃), 3.89 (dd, J = 10.8, 7.0 Hz, 1H_c), 4.22 (q, 2H, J = 7.2 Hz, CH₂ of CH₂CH₃), 4.79 (dd, J = 10.8, 9.0 Hz, 1H_a), 6.72–7.59 (m, 12H, Ar-H), 7.65 (s, 1H, CH=), 10.41 (s, 1H, D₂O-exchangeable, NH). ¹³C-NMR (DMSO-d₆): δ 13.9, 29.6, 38.0, 43.4, 46.9, 54.9, 55.9, 56.2, 59.3, 64.2, 76.2, 113.4, 114.1, 121.3, 124.2, 126.3, 127.3, 128.4, 129.4, 129.6, 133.4, 136.1, 138.3, 139.6, 152.8, 154.2, 157.6, 159.8, 172.0, 202.5. MS m/z (%): 583 (M⁺ + 2, 4), 582 (M⁺ + 1, 35), 581 (M⁺, 90), 244 (10), 206 (8), 95 (19). Anal. For C₃₄H₃₅N₃O₆ (581.67): calcd. C, 70.21; H, 6.07; N, 7.22. Found C, 70.19; H, 6.10; N, 7.20.

Ethyl 1-N-methyl-spiro[2.3′]oxindole-spiro[3.3′′]5′′-(3,4-dichloro)benzylidene-1′′-N-carboxylate-4′′- piperidinone-4-(3,4 dichloro)phenyl-pyrrolidine (6f). Yellow crystals, m.p. 213–214 °C (Dioxane);; IR (cm⁻¹): 3400 (NH), 1715, 1713, 1692 (3CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.12 (t, 3H, J = 7.1 Hz, CH₃ of CH₂CH₃), 1.98 (s, 3H, NCH₃), 3.18 (dd, J = 9.1, 7.0 Hz, 1H_b), 3.30, 3.45 (2s, 4H, 2CH₂ of piperidinone ring), 3.88 (dd, J = 10.6, 7.0 Hz, 1H_c), 4.28 (q, 2H, J = 7.1 Hz, CH₂ of CH₂CH₃), 4.73 (dd, J = 10.6, 9.1 Hz, 1H_a), 6.80–7.65 (m, 10H, Ar-H), 7.66 (s, 1H, CH=), 10.4 (s, 1H, D₂O-exchangeable, NH). ¹³C-NMR (DMSO-d₆): δ 13.6, 29.2, 38.2, 42.9, 46.7, 54.7, 59.3, 63.2, 76.1, 121.6, 124.1, 126.4, 127.9, 129.5, 129.8, 128.9, 130.2, 130.3, 136.1, 132.5, 132.6, 133.4, 134.8, 137.8, 139.5, 140.6, 153.9, 154.5, 173.1, 202.8. MS m/z (%): 661 (M⁺ + 2, 48), 660 (M⁺ + 1, 34.5), 659 (M⁺, 89), 657 (70), 357 (10), 339 (20), 338 (5), 145 (5). Anal. For C₃₂H₂₇Cl₄N₃O₄ (659.38): calcd. C, 58.29; H, 4.13; N, 6.37.Found C, 58.28; H, 4.11; N, 6.36.

Ethyl 1-N-methyl-spiro[2.3′]oxindole-spiro[3.3′′]5′′-(2,4-difluoro)-benzylidene-1′′-N-carboxylate-4′′-piperidinone-4-(2,4-difluoro)phenyl-pyrrolidine (6g). Yellow crystals, m.p. 130–132 °C (EtOH/Dioxane); IR: 3255 (NH), 1716, 1692, 1660 (3CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.15 (t, 3H, J = 7.2 Hz, CH₃ of CH₂CH₃), 1.98 (s, 3H, NCH₃), 3.29 (dd, J = 9.0, 7.0 Hz, 1H_b), 3.34, 3.46 (2s, 4H, 2CH₂ of piperidinone ring), 3.82 (dd, J = 10.7, 7.0 Hz, 1H_c), 4.29 (q, 2H, J = 7.2 Hz, CH₂ of CH₂CH₃), 4.73 (dd, J = 10.7, 9.0 Hz, 1H_a), 6.73–7.21 (m, 10H, Ar-H), 7.52 (s, 1H, CH=), 10.52 (br., 1H, D₂O-exchangeable, NH). MS m/z (%): 595 (M⁺ + 2, 6), 594 (M⁺ + 1, 35), 593 (M⁺, 78), 339 (20), 325 (8), 306 (7), 113 (5). Anal. For C₃₂H₂₇F₄N₃O₄ (593.58): calcd. C, 64.75; H, 4.59; N, 7.08. Found: C, 64.69; H, 4.50; N, 7.02.

Ethyl 1-N-methyl-spiro[2.3′]oxindole-spiro[3.3′′]5′′-(3,4-dimethoxy)benzylidene-1′′-N-carboxylate-4′′-piperidinone-4-(3,4-dimethoxy)phenyl-pyrrolidine (6h). Brown crystals, m.p. 95–98 °C (Methanol); IR: 3260 (NH), 1712, 1695, 1659 (3CO) cm⁻¹. ¹H-NMR (DMSO-d₆); δ 1.18 (t, 3H, J = 6.9 Hz, CH₃ of CH₂CH₃), 2.04 (s, 3H, NCH₃), 3.23 (dd, J = 9.0, 7.0 Hz, 1H_b), 3.33, 3.47 (2s, 4H, 2CH₂of piperidinone ring), 3.67, 3.69 (2s, 6H, 2OCH₃), 3.79, 3.82 (2s, 6H, 2OCH₃), 3.87 (dd, J = 10.5, 7.0 Hz, 1H_c), 4.22 (q, 2H, J = 6.9 Hz, CH₂ of CH₂CH₃), 4.69 (dd, J = 10.5, 9.0 Hz, 1H_a), 6.55–7.59 (m, 10H, Ar-H), 7.62 (s, 1H, CH=), 10.3 (s, 1H, D₂O-exchangeable, NH). ¹³C-NMR (75 MHz, δ ppm, DMSO-d₆); 13.9, 29.7, 37.8, 43.1, 46.9, 54.7, 56.3, 56.4, 56.8, 56.9, 59.0, 63.8, 76.7, 111.5, 113.7, 114.7, 115.4, 119.8,120.2, 121.5, 124.5, 126.3, 128.4, 128.6, 134.4, 136.0, 137.8, 139.7, 146.6, 148.9, 149.0, 149.8, 152.9, 154.5, 172.2, 204.1. MS m/z (%): 643 (M⁺ + 2, 8), 642 (M⁺ + 1, 39), 641 (M⁺, 70), 329 (10), 318 (9), 137 (4). Anal. For C₃₆H₃₉N₃O₈ (641.72): calcd. C, 67.38; H, 6.13; N, 6.55. Found: C, 67.31; H, 6.08; N, 6.48.

Ethyl 1-N-methyl-spiro[2.3′]oxindole-spiro[3.3′′]5′′-(4-trifluro-methyl)benzylidene-1′′-N-carbo-xylate-4′′-piperidinone-4-(4-trifluro-methyl)phenyl-pyrrolidine (6i). Green crystals, m.p. 136–137 °C (EtOH/Dioxane); IR: 3367 (NH), 1709, 1701, 1654 (3CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.15 (t, 3H, J = 7.2 Hz, CH₃ of CH₂CH₃), 2.09 (s, 3H, NCH₃), 3.24 (dd, J = 9.0, 7.0 Hz, 1H_b), 3.32, 3.46 (2s, 4H, 2CH₂of piperidinone ring), 3.82 (dd, J = 10.7, 7.0 Hz, 1H_c), 4.23 (q, 2H, J = 7.2 Hz, CH₂ of CH₂CH₃), 4.76 (dd, J = 10.7, 9.0 Hz, 1H_a), 6.51–7.71 (m, 12H, Ar-H), 7.75 (s, 1H, CH=), 10.39 (s, 1H, D₂O-exchangeable, NH). MS m/z (%): 659 (M⁺ + 2, 7), 658 (M⁺ + 1, 39), 657 (M⁺, 90), 344 (12), 339 (20), 145 (8). Anal. For C₃₄H₂₉F₆N₃O₄ (657.61): calcd. C, 62.1; H, 4.44; N, 6.39.Found: C, 62.13; H, 4.36; N, 6. 37.

Ethyl 1-N-methyl-spiro[2.3′]oxindole-spiro[3.3′′]5′′-(3,4,5-trimethoxy)benzylidene-1′′-N-carboxylate-4′′-piperidinone-4-(3,4,5-trimethoxy)phenyl-pyrrolidine (6j). Yellow crystals, m.p. 115–116 °C (EtOH/Dioxane); IR: 3309 (NH), 1715, 1696, 1655 (3CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.20 (t, 3H, J = 7 Hz, CH₃ of CH₂CH₃), 2.12 (s, 3H, NCH₃), 3.26 (dd, J = 9.0, 7.0 Hz, 1H_b), 3.27, 3.44 (2s, 4H, 2CH₂ of piperidinone ring), 3.69, 3.71 (2s, 6H, 2OCH₃), 3.74, 3.75 (2s, 6H, 2OCH3), 3.80, 3.82 (2s, 6H, 2OCH₃), 3.87 (dd, J = 10.7, 7.0 Hz, 1H_c), 4.23 (q, 2H, J = 7 Hz, CH₂ of CH₂CH₃), 4.75 (dd, J = 10.7, 9.0 Hz, 1H_a), 6.43–6.81 (m, 8H, Ar-H), 7.25 (s, 1H, CH=), 9.88 (s, 1H, D₂O-exchangeable, NH). MS m/z (%): 703 (M⁺ + 2, 9), 702 (M⁺ + 1, 43), 701 (M⁺, 92), 364 (12), 368 (19), 339 (20) 167 (7). Anal. For C₃₈H₄₃N₃O₁₀ (701.77): calcd. C, 65.04; H, 6.18; N, 5.99. Found C, 64.95; H, 6.11; N, 5.92.

3.4. General Synthesis of Dispiropyrrolizine Oxindole Derivatives (8a–j)

A reaction mixture of isatin 1 (1.47 g, 1.0 mmol), l-proline 7 (1.15 g, 10 mmol), and ethyl 3,5-bis(aryl-methylidene)-N-carboxyl-4-piperidinone 4a–j (1.0 mmol), was producedby refluxing it in methanol for 120 min at 60 °C, and was then poured on water. The solid that formed was collected and crystallized from suitable solvent to get white to green crystals of compounds 8a–j.

Ethyl spiro[3.3′′]-oxindole-spiro[2.3′]1'-carboxylate-5'-phenylmethylidene-tetra-hydro-4'(1H)-piperidinone-1-phenyl-hexahydro-1H-pyrrolizine (8a). Yellow crystals, m.p. 127–128 °C (EtOH/Dioxane); IR: 3251 (NH), 1720, 1690, 1600 (3CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.15 (t, 3H, J = 6.9 Hz, CH₃ of CH₂CH₃), 1.78–1.90 (m, 4H, 2CH₂ of pyrrolizline), 2.40–2.48 (m, 2H, CH₂ of pyrrolizine), 2.51–2.55 (m, 1H_b), 3.26 (d, J = 10.1 Hz, 1H_a), 3.53, 3.77 (2s, 4H, 2CH₂ of piperidinone ring), 4.11 (q, 2H, J = 6.9 Hz, CH₂ of CH₂CH₃), 6.68-7.53 (m, 14H, Ar-H), 7.64 (s, 1H, CH=), 8.53 (br, 1H, D₂O-exchangeable, NH).¹³C-NMR (DMSO-d₆): δ 13.9, 24.2, 28.5, 51.6, 32.7, 42.9, 46.6, 59.2, 61.1, 62.1, 71.4, 121.5, 124.5, 126.2, 126.3, 126.6, 128.2, 128.3, 128.4, 128.5, 128.7, 135.7, 136.1, 137.5, 139.4, 139.5, 152.9, 154.5, 173.2, 199.2. MS m/z (%): 549 (M⁺ + 2, 5), 548 (M⁺ + 1, 37), 547 (M⁺, 65), 470 (3), 457 (9), 412 (5), 302 (34), 257 (30), 206 (10), 158 (9), 97 (8), 77 (3). Anal. For C₃₄H₃₃N₃O₄ (547.65): calcd. C, 74.57; H, 6.07; N, 7.67. Found C, 74.33; H, 6.1; N, 7.6.

Ethyl spiro[3.3′′]-oxindole-spiro[2.3′]1'-carboxylate-5'-(4-nitro)phenylmethylidene-tetrahydro-4'(1H)-piperidinone-1-(4-nitro)phenyl-hexahydro-1H-pyrrolizine (8b). Yellow crystals, m.p. 160–161 °C (Dioxane); IR: 3255 (NH), 1701, 1692, 1620 (3CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.15 (t, 3H, J = 7 Hz, CH₃ of CH₂CH₃), 1.78–1.98 (m, 4H, 2CH₂ of pyrrolizline), 2.32–2.38 (m, 2H, CH₂ of pyrrolizine), 2.71–2.75 (m, 1H_b), 3.28 (d, J = 10.3 Hz, 1H_a), 3.52, 3.71 (2s, 4H, 2CH₂ of piperidinone ring), 4.21 (q, 2H, J = 7 Hz CH₂ of CH₂CH₃), 6.76–7.52 (m, 12H, Ar-H), 7.66 (s, 1H, CH=), 8.62 (br, 1H, D₂O-exchangeable, NH). ¹³C-NMR (DMSO-d₆): δ 13.9, 23.7, 29.5, 31.6, 42.5, 46.7, 50.6, 59.1, 60.9, 61.5, 71.2, 120.9, 121.1, 121.4, 124.3, 126.5, 127.4, 128.3, 129.2, 136.0, 137.8, 139.7, 141.3,145.3, 145.7, 147.7, 152.7, 154.6, 172.6, 203.2. MS m/z (%): 639 (M⁺ + 2, 10), 638 (M⁺ + 1, 35), 637 (M⁺, 89), 503 (9), 494 (4), 242 (12), 205 (9), 122 (5), 97 (10). Anal. For C₃₄H₃₁N₅O₈ (637.65): calcd. C, 64.04; H, 4.90; N, 10.98. Found: C, 63.96; H, 4.84; N, 10.86.

Ethyl spiro[3.3′′]-oxindole-spiro[2.3′]1'-carboxylate-5'-(4-chloro)phenylmethylidene-tetrahydro-4'(1H)-piperidinone-1-(4-chloro)phenyl-hexahydro-1H-pyrrolizine (8c). Yellow crystals, m.p. 128–129 °C (EtOH/Dioxane); IR: 3251 (NH), 1701, 1678, 1616 (3CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.15 (t, 3H, J = 7.4 Hz, CH₃ of CH₂CH₃), 1.78–1.89 (m, 4H, 2CH₂of pyrrolizline), 2.33–2.38 (m, 2H, CH₂ of pyrrolizine), 2.51–2.56 (m, 1H_b), 3.35 (d, J = 10.4 Hz, 1H_a), 3.78, 3.84 (2s, 4H, 2CH₂ of piperidinone ring), 4.39 (q, 2H, J = 7.4 Hz, CH₂ of CH₂CH₃), 6.72–7.49 (m, 12H, Ar-H), 7.56 (s, 1H, CH=), 8.48 (s, 1H, D₂O-exchangeable, NH). ¹³C-NMR (DMSO-d₆): δ 13.7, 23.8, 29.2, 32.0, 42.5, 46.0, 51.5, 59.0, 60.8, 61.8, 71.1, 121.4, 124.3, 126.7, 127.8, 128.0, 128.6, 128.9, 129.6, 131.6, 133.4, 133.7, 136.3, 137.4, 137.6, 139.8, 152.7, 154.4, 172.5, 200.2. MS m/z (%): 617 (M⁺ + 2, 67), 616 (M⁺ + 1, 59), 615 (M⁺, 80), 494 (7), 482 (14), 337 (20), 292 (15), 219 (8), 206 (20), 97 (10), 57 (6). Anal. For C₃₄H₃₁Cl₂N₃O₄ (616.54): calcd. C, 66.24; H, 5.07; N, 6.82. Found: C, 66.13; H, 5.02; N, 6.80.

Ethyl spiro[3.3′′]-oxindole-spiro[2.3′]1'-carboxylate-5'-(4-fluoro)phenylmethylidene-tetrahydro-4'(1H)-piperidinone-1-(4-fluoro)phenyl-hexahydro-1H-pyrrolizine (8d). White crystals, m.p. 185–187 °C (Dioxane); IR: 3394 (NH), 1715, 1692, 1620 (3CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.18 (t, 3H, J = 7.2 Hz, CH₃ of CH₂CH₃),1.75–1.96 (m, 4H, 2CH₂ of pyrrolizline), 2.49–2.55 (m, 2H, CH₂ of pyrrolizine), 2.51–2.57 (m, 1H_b), 3.26 (d, J = 10.2 Hz, 1H_a), 3.46, 3.77 (2s, 4H, 2CH₂ of piperidinone ring), 4.24 (q, 2H, J = 7.2 Hz, CH₂ of CH₂CH₃), 6.79–7.35 (m, 12H, Ar-H), 7.36 (s, 1H, CH=), 8.35 (s, 1H, D₂O-exchangeable, NH). ¹³C-NMR (DMSO-d₆): δ 13.7, 23.9, 28.9, 32.7, 42.4, 46.8, 50.8, 59.0, 60.8, 61.6, 71.2, 115.2, 115.3, 121.3, 124.2, 126.0, 128.2, 128.2, 129.9, 130.8,134.9, 136.5, 137.3, 139.7, 152.8, 154.4, 160.3, 162.2,173.1, 199.9. MS m/z (%): 585 (M⁺ + 2, 7), 584 (M⁺ + 1, 37), 583 (M⁺, 86), 206 (10), 97 (10). Anal. For C₃₄H₃₁F₂N₃O₄ (583.64): calcd. C, 69.97; H, 5.35; N, 7.20. Found: C, 69.90; H, 5.28; N, 7.15.

Ethyl spiro[3.3′′]-oxindole-spiro[2.3′]1'-carboxylate-5'-(4-methoxy)phenylmethylidene-tetrahydro-4'(1H)-piperidinone-1-(4-methoxy)phenyl-hexahydro-1H-pyrrolizine (8e). Yellow crystals, m.p. 158–160 °C (EtOH/Dioxane); IR: 3421 (NH), 1715, 1662, 1600 (3CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.14 (t, 3H, J = 6.9 Hz, CH₃ of CH₂CH₃), 1.78–1.96 (m, 4H, 2CH₂ of pyrrolizline), 2.44–2.50 (m, 2H, CH₂ of pyrrolizine), 2.59–2.65 (m, 1H_b), 3.25 (d, J = 10.2 Hz, 1H_a), 3.68, 3.82 (2s, 4H, 2CH₂ of piperidinone ring), 3.69,3.75 (2s, 6H, 2OCH₃), 4.25 (q, 2H, J = 6.9 Hz, CH₂ of CH₂CH₃), 7.05–7.52 (m, 12H, Ar-H), 7.65 (s, 1H, CH=), 8.8 (s, 1H, D₂O- exchangeable, NH). ¹³C-NMR (DMSO-d₆): δ 13.8, 24.1, 29.1, 32.5 , 42.5, 46.7, 50.6, 56.1, 58.8, 58.9, 60.8, 61.6, 71.2, 114.2, 114.3, 121.5, 124.1, 126.9, 127.5, 127.7, 128.2, 129.2, 131.7, 136.3, 137.2, 139.6, 152.7, 154.2, 157.9, 159.9, 173.0, 202.2. MS m/z (%): 609 (M⁺ + 2, 8), 608 (M⁺ + 1, 97), 607 (M⁺, 45), 333 (20), 288 (30), 215 (15), 120 (8). Anal. For C₃₆H₃₇N₃O₆ (607.71): calcd. C, 71.15; H, 6.14; N, 6.91. Found: C, 71.13; H, 6.12; N, 6.87.

Ethyl spiro[3.3′′]-oxindole-spiro[2.3′]1'-carboxylate-5'-(3,4-dichloro)phenylmethylidene-tetrahydro-4'(1H)-piperidinone-1-(3,4-dichloro)phenyl-hexahydro-1H-pyrrolizine (8f). White crystals, m.p. 158–159 °C (EtOH/Dioxane); IR: 3255 (NH), 1701, 1681, 1620 (3CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.16 (t, 3H, J = 7.2 Hz, CH₃ of CH₂CH₃), 1.77–1.98 (m, 4H, 2CH₂ of pyrrolizline), 2.46–2.52 (m, 2H, CH₂ of pyrrolizine), 2.55–2.75 (m, 1H_b), 3.26 (d, J = 10.2 Hz, 1H_a), 3.34, 3.62 (2s, 4H, 2CH₂ of piperidinone ring), 4.32 (q, 2H, J = 7.2 Hz, CH₂ of CH₂CH₃), 6.79–7.35 (m, 10H, Ar-H), 7.38 (s, 1H, CH=), 8.45 (s, 1H, D₂O-exchangeable, NH). MS m/z (%): 685 (M⁺, 49), 684 (100), 683 (78), 371 (21), 353 (14), 327 (14), 143 (8). Anal. For C₃₄H₂₉Cl₄N₃O₄ (685.42) calcd. C, 59.58; H, 4.26; N, 6.13. Found: C, 59.56; H, 4.19; N, 6.07.

Ethyl spiro[3.3′′]-oxindole-spiro[2.3′]1'-carboxylate-5'-(2,4-difluoro)phenylmethylidene-tetrahydro-4'(1H)-piperidinone-1-(2,4-difluoro)phenyl-hexahydro-1H-pyrroliz-ine (8g). Pale green crystals, m.p. 132–133 °C (Methanol); IR: 3433 (NH), 1705, 1681, 1616 (3CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.13 (t, 3H, J = 7.4 Hz, CH₃ of CH₂CH₃), 1.72–1.89 (m, 4H, 2CH₂ of pyrrolizline), 2.42–2.49 (m, 2H, CH₂ of pyrrolizine), 2.69–2.75 (m, 1H_b), 3.30 (d, J = 10.0 Hz, 1H_a), 3.45, 3.88 (2s, 4H, 2CH₂ of piperidinone ring), 4.30 (q, 2H, J = 7.4 Hz, CH₂ of CH₂CH₃), 6.71–7.61 (m, 10H, Ar-H), 7.66 (s, 1H, CH=), 8.48 (s, 1H, D₂O-exchangeable, NH). MS m/z (%): 621 (M⁺ + 2, 7), 620 (M⁺ + 1, 38), 619 (M⁺, 55), 294 (23), 393 (9), 221 (4), 93 (4). Anal. for C₃₄H₂₉F₄N₃O₄ (619.62): calcd. C, 65.91; H, 4.72; N, 6.78. Found: C, 65.88; H, 4.68; N, 6.73.

Ethyl spiro[3.3′′]-oxindole-spiro[2.3′]1'-carboxylate-5'-(3,4-dimethoxy)phenylmethylidene-tetrahydro-4'(1H)-piperidinone-1-(3,4-dimethoxy)phenyl-hexahydro-1H-pyrro-lizine (8h). Yellow crystals, m.p. 231–233 °C (EtOH/Dioxane); IR: 3421 (NH), 1700, 1697, 1616 (3CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.14 (t, 3H, J = 7.1 Hz, CH₃ of CH₂CH₃), 1.78–2.02 (m, 4H, 2CH₂ of pyrrolizline), 2.38–2.48 (m, 2H, CH₂ of pyrrolizine), 2.59–2.73 (m, 1H_b), 3.33 (d, J = 10 Hz, 1H_a), 3.52, 3.65 (2s, 4H, 2CH₂of piperidinone ring), 3.69, 3.71 (2s, 6H, 2OCH₃), 3.79, 3.82 (2s, 6H, 2OCH₃), 4.21 (q, 2H, J = 7.1 Hz, CH₂ of CH₂CH₃), 6.79–7.65 (m, 10H, Ar-H), 7.72 (s, 1H, CH=), 8.31 (s, 1H, D₂O-exchangeable, NH). ¹³C-NMR (DMSO-d₆): δ 13.7, 23.6, 29.5, 31.9, 42.5, 46.6, 50.9, 56.2, 56.4, 56.7, 56.8, 59.5, 61.3, 61.4, 71.3, 111.7, 113.2, 115.2, 119.8, 121.6, 121.2, 124.7, 126.5, 128.4, 128.5, 132.6, 136.4, 137.3, 139.2, 147.2, 149.1, 149.7, 149.9, 152.9, 154.5, 173.0, 200.9. MS m/z (%): 669 (M⁺ + 2, 10), 668 (M⁺ + 1, 43), 667 (M⁺, 92), 362 (31), 318 (9), 243 (10), 90 (20), 93 (10). Anal. For C₃₈H₄₁N₃O₈ (667.76): calcd. C, 68.35; H, 6.19; N, 6.29. Found C, 68.28; H, 6.14; N, 6.24.

Ethyl spiro[3.3′′]-oxindole-spiro[2.3′]1'-carboxylate-5'-(4-trifluromethyl)phenyl-methylidene-tetrahydro-4'(1H)-piperidinone-1-(4-trifluromethyl)phenyl-hexahydro-1H-pyrrolizine (8i). Green crystals, m.p. 137–139 °C (EtOH/Dioxane); IR: 3371 (NH), 1701, 1690, 1616 (3CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.18 (t, 3H, J = 7 Hz, CH₃ of CH₂CH₃), 1.76–1.98 (m, 4H, 2CH₂ of pyrrolizline), 2.46–2.50 (m, 2H, CH₂ of pyrrolizine), 2.59–2.74 (m, 1H_b), 3.96 (d, J = 10.3 Hz, 1H_a), 3.35, 3.77 (2s, 4H, 2CH₂ of piperidinone ring), 4.32 (q, 2H, J = 7 Hz, CH₂ of CH₂CH₃), 6.79–7.35 (m, 12H, Ar-H), 7.42 (s, 1H, CH=), 8.42 (s, 1H, D₂O-exchangeable, NH).MS m/z (%): 685 (M⁺ + 2, 7), 684 (M⁺ + 1, 39), 683 (M⁺, 92), 370 (13), 325 (7), 251 (13), 145 (6). Anal. For C₃₆H₃₁F₆N₃O₄ (683.65): calcd. C, 63.25; H, 4.57; N, 6.15. Found: C, 63.18; H, 4.51; N, 6.08.

Ethyl spiro[3.3′′]-oxindole-spiro[2.3′]1'-carboxylate-5'-(3,4,5-trimethoxy)phenyl-methylidene-tetrahydro-4'(1H)-piperidinone-1-(3,4,5-trimethoxy)phenyl-hexahydro-1H-pyrrolizine (8j). Yellow crystals, m.p. 123–124 °C (EtOH/Dioxane); IR: 3464 (NH), 1701, 1692, 1620 (3CO) cm⁻¹. ¹H-NMR (DMSO-d₆): δ 1.15 (t, 3H, J = 6.9 Hz, CH₃ of CH₂CH₃), 1.82–2.09 (m, 4H, 2CH₂ of pyrrolizline), 2.44–2.50 (m, 2H, CH₂ of pyrrolizine), 2.72–2.80 (m, 1H_b), 3.25 (d, J = 10.1 Hz, 1H_a), 3.46, 3.65 (2s, 4H, 2CH₂ of piperidinone ring), 3.69, 3.71 (2s, 6H, 2OCH₃), 3.74,3.76 (2s, 6H, 2OCH₃), 3.82, 3.84 (2s, 6H, 2OCH₃), 4.19 (q, 2H, J = 6.9 Hz, CH₂ of CH₂CH₃), 6.39–7.55 (m, 8H, Ar-H), 7.62 (s, 1H, CH=), 8.37 (s, 1H, D₂O-exchangeable, NH). MS m/z (%): 729 (M⁺ + 2, 2), 728 (M⁺ + 1, 10), 727 (M⁺, 42), 726 (94), 347 (19), 392 (25), 275 (17), 167 (9). Anal. For C₄₀H₄₅N₃O₁₀ (727.81): calcd. C, 66.01; H, 6.23; N, 5.77. Found: C, 65.94; H, 6.14; N, 5.65.

3.5. Microbiological Assay

An agar diffusion well method was used to determine the antimicrobial activity. The microorganism inoculums were uniformly spread using a sterile cotton swab on a sterile Petri dish containing Malt extract agar (for fungi) and nutrient agar (for bacteria). Each sample (100 μL) was added to each well (6 mm diameter holes cut in the agar gel, 20 mm apart from one another). The systems were incubated for 24–48 h at 37 °C (for bacteria) and at 28 °C (for fungi). After incubation, microorganism growth was observed. The inhibition of bacterial and fungal growth was measured in mm. Tests were performed in triplicate [26].

4. Conclusions

In conclusion, we synthesized new derivatives of spirooxindole-spiropiperidinone- pyrrolidinesnd-spirooxindole-spiropiperidinone-pyrrolizinesthrougha 1,3-dipolar cycloaddition reaction of azomethineylides, generated from isatin, sarcosine, and l-proline through a decarboxylative route with dipolarophile 4a–j. All of the newly synthesized compounds were evaluated for their antimicrobial activities and the minimum inhibitory concentration (MIC) of the most active compounds against the test organisms. Four compounds from the series have emerged as potent antibacterial and antifungal agents.