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Article

Utility of Sulphones in Heterocyclic Synthesis: Synthesis of Some Pyridine, Chromene and Thiophene Derivatives

1
Department of Chemistry, Faculty of Science, Mansoura University, Mansoura, Egypt
2
Department of Chemistry, Faculty of Education, Suez Canal University, Al-Arish, Egypt
3
National Research Cente Dokki, Cairo, Egypt
*
Author to whom correspondence should be addressed.
Molecules 2000, 5(5), 701-709; https://doi.org/10.3390/50500701
Submission received: 3 August 1999 / Revised: 13 October 1999 / Accepted: 13 October 1999 / Published: 5 May 2000

Abstract

:
Phenylsulfonylacetonitrile (1) when reacted with α,β-unsaturated nitriles (2a,b) and/or 2-hydroxynaphthaldehyde yields pyridine derivatives (3a,b) and / or the imino-chromene derivative (4) respectively. The behavior of (1) towards some α-halogenated compounds has been investigated.

Introduction

This work is the continuation of a program with the aim to develop new simple methods for the synthesis of functionally substituted heterocycles with anticipated biological activity. We have recently extended it to include the investigation of the pharmacological aspects of the newly synthesized he-terocycles based on the finding that some heterocycles can achieve activity in both the pharmacologi-cal and pesticidal areas, e.g. thiabenzdazole, the well known human and veterinary anthelmentic, is also used as a fungicide [1,2].

Results and Discussion

Pyridines and chromene derivatives have recently received considerable attention due to their syn-thetic and pharmaceutical importance and different approaches for their synthesis have been developed [3,5a-c]. In the last few years the authors have been exploring the synthetic potential, scope, and limi-tations of activated nitriles in heterocyclic synthesis [6,7,8]. Several new approaches for the synthesis of five and six membered rings and their fused heterocyclic derivatives have been developed during this work [9,10]. In the present work we explore the synthetic potential of phenylsulfonyl-acetonitrile (1) to form polysubstituted pyridines and chromene heterocycles via the reaction of 1 with α,β-unsaturated nitriles (2a,b) and 2-hydroxynaphthaldehyde respectively.
Thus, compound 1 reacts under TEA catalysis with α,β-unsaturated nitriles (2a,b) in refluxing ethanol to afford 2-amino-3-phenylsulfonyl-4-aryl-5-carbonitrile pyridines 3a,b as coloured solid products [11]. The IR spectrum of these products showed in each case, absorption bands at ν 3350-3400, 2220, and 1610 cm-1 corresponding to NH2, CN, and C=N groups respectively. Structures 3a,b were assigned to these products on the basis of the spectral as well as analytical data (cf. Table 1). The 1H-NMR spectrum of 3a revealed a broad singlet at δ 6.5 ppm assigned to the amine protons and a multiplet at δ 7.8-8.4 ppm assigned to the pyridine-2H and aromatic protons.
Scheme 1.
Scheme 1.
Molecules 05 00701 sch001
Compound (1) reacts with 2-hydroxy naphthaldehyde in refluxing ethanol in the presence of TEA to give 2-imino-3-phenylsulfonyl-benzo[f]chromene (4) in high yield. Mass spectral measurements and analytical data are in complete agreement with structure 4 (M+ 335). Moreover, the resulting coumarin derivatives have latent functional substituents, which have the potential for further chemical transfor-mations giving new routes for the preparation of substituted coumarin derivatives with possible bio-logical activity. 3-Phenylsulfonyl-2H-benzo[f]-2-chromenone (5) was synthesized via hydrolysis of (4) in a mixture of conc. hydrochloric acid and ethanol. The mass spectrum of (5) showed the expected molecular formula C19H12O4S (M+ 336).
Previously, we investigated the reaction of phenyl isothiocyanate with active methylene compounds in alkaline medium, which has proved to be a convenient route for the synthesis of thiazole, pyrazole, oxazine and pyrimidine ring systems [7]. Now, we have extended our synthetic program to the synthe-sis of otherwise inaccessible heterocyclic ring systems, utilizing phenyl isothiocyanate as a key starting material. It is known that a great variety of reactants bearing the N=C=S fragment undergo cyclization on reaction with α-halocarbonyl compounds to afford thiazoles, 2,3-dihydrothiazoles and thiazolidines [12], which have been shown to exhibit local anaesthetic [13], antiprotozoal [14] and fungicidal properties [15]. In this paper, we describe a generally applicable extension of this synthetic approach, first reported by Hantzsch and Weber [16]. Thus, the base-prompted reaction of the acidic methylene com-pound 1 with phenyl isothio-cyanate in dry DMF at room temperature yields the non-isolable interme-diate 6. Treatment of 6 with α-chloroacetamide in boiling DMF yielded a product (8), which analyzed correctly for C17H15N3O3S2. The structure 8 was inferred from its spectral data. Thus, the IR spectrum showed absorption bands at ν 3450, 3150, 1661, 1550, 1270 and 1180 cm-1 corresponding to NH2, NH, C=O, Ph and SO2 functions and the absence of a CN stretching band. Its 1H-NMR spectrum showed a broad singlet at δ 5.5-6.2 ppm (4H), two multiplet signals integrated for (10 H) centered at 7.4 and 8.0 (aromatic protons) and a singlet (1H) at 8.6. On shaking the compound with D2O, the broad band sig-nals at δ 5.5-6.2 ppm and 8.6 disappeared . Based on the foregoing data, structure 8 was assigned to this product. The structure of 8 was further confirmed by its alternative synthesis. Thus, it was found that, treatment of 6 with α-chloroacetamide in refluxing ethanol produced the acyclic intermediate 7. Structure 7 was suggested for the reaction product on the basis of both elemental and spectral analysis. The IR spectrum showed the presence of a cyano absorption band at ν 2220 cm-1, NH2, NH and C=O (amidic) functions at ν 3340, 3150 and 1680 cm-1 respectively. Refluxing 7 in ethanol with a few drops of TEA led to the formation of a product identical in all respects (m.p., mixed m.p., IR, 1H-NMR) to 8.
Scheme 2.
Scheme 2.
Molecules 05 00701 sch002
The intermediate 6 also undergoes in-situ cyclization upon the reaction with equimolar amounts of phenacyl bromide in boiling ethanol and a catalytic amount of TEA, giving a yellow colored product (10). The phenylsulfonyl thiophene structure 10 was suggested for this product on the basis of analyti-cal and spectral data (cf. Table 1). The mass spectrum of 10 showed molecular formula C23H18N2O3S2 (M+ = 434). The reaction may occur through the non-isolable intermediacy of a cyclic derivative (9). Attempts to isolate 9 by refluxing phenacyl bromide with the intermediate 6 in ethanol were unsuc-cessful. Compound 10 is assumed to be formed via the acyclic intermediate 9.
Compound 6 reacted readily with chloroacetone in boiling ethanol to afford the acyclic intermediate 11 by NaCl elimination. Refluxing 11 in ethanol with a catalytic amount of TEA, gave the thiophene derivative 12 whose structure was confirmed by elementary analysis and spectral data. (cf. Table 1). The structure of 12 was further confirmed by its alternative synthesis. Thus, refluxing 6 with chloro-acetone in DMF affords the thiophene derivative 12 in reasonably good yield. Similarly, when the in-termediate 6 is treated with chloroacetonitrile in refluxing ethanol the corresponding acyclic interme-diate 13 is exclusively isolated in good yield. The structure of 13 has been confirmed on the basis of elemental and spectral data. e.g. the IR spectrum exhibits bands at ν 3200 (NH), 2220, 2195 cm-1 (two cyano). Its 1H-NMR spectrum reveals a CH2 signal at δ 3.23 ppm. Furthermore, heating of the interme-diate 13 in ethanol containing a catalytic amount of TEA affords the thiophene derivative 14. The thio-phene structure 14 was established based on its IR spectrum which showed bands related to NH2, NH and CN functions. Its 1H-NMR spectrum reveals a multiplet at (δ ppm) 7.31-7.56 (10 H, aromatic), broad signals at δ 6.5 (2H, NH2) and δ 8.7 ppm (1H, NH). On the other hand, it has been found that it is directly formed by refluxing 6 and chloroacetonitrile in DMF.
Scheme 3.
Scheme 3.
Molecules 05 00701 sch003
When 6 was treated with an equimolar amount of chloroacetyl chloride or with chloroacetic acid in boiling ethanol, a product that analyzed for C19H18N2O4S 2 was isolated in each case in good yield. The acyclic structure 15 was established based on its IR spectrum that showed bands related to NH, CN and CO functions. Its 1 H-NMR spectrum reveals a multiplet at (δ ppm) 7.5-8.56 (10 H, aromatic), a triplet signal at δ 1.3 (3H, CH3), singlet at δ 3.7 ( 2H ), quartet at δ 4.3 ( 2H, CH2) and a D2O exchangeable NH at 8.91 ppm. Alternatively, treatment of 6 with ethyl bromoacetate in refluxing ethanol gives a single product, which is identical in all respects to 15 (m.p., mixed m.p. and IR spectrum). The mass spectrum of 15 showed a molecular formula C19H18N2O4S2 (M+ = 402). Refluxing of 15 in ethanol with a catalytic amount of TEA afforded the corresponding thiophene derivative 16 [16] (cf. Table 1).

Conclusion

We report a facile route for the formation of pyridines, chromenes and thiophene derivatives based on sulfones.

Experimental

General

All melting points are uncorrected. FTIR spectra (KBr disk) were recorded on a Nicolet Magna-IR model 550 spectrophotometer, 1H NMR spectra in CDCl3 were determined on a Brucker WPSY 200 MHZ spectrometer with TMS as internal standard, and the chemical shifts are in δ ppm. Mass spectra were recorded at 70 ev with a Varian MAT 311

Synthesis of pyridine derivatives (3a,b). General procedure

A mixture of phenylsulfonylacetonitrile (1) (0.01 mol), α,β-unsaturated nitriles 2a,b (0.01 mol) and catalytic amounts of TEA in ethanol (15 mL) were refluxed for 6 h. The solid product obtained after cooling was filtered off and recrystallized from ethanol to give the pyridine derivatives 3a,b (cf. Table 1).

Synthesis of 2- imino-3-phenylsulfonyl-2H-benzo[ f ]chromene (4)

A mixture of phenylsulfonylacetonitrile (1) (0.01 mol), 2-hydroxy-1-naphthaldehyde (0.01 mol) and a catalytic amount of TEA in ethanol (15 mL) was refluxed for 2 h. The solid product iminochromene 4 obtained after cooling was recrystallized from ethanol. (cf. Table 1).

Synthesis of 3-phenylsulfonyl-2H-benzo[ f ]-2-chromenone (5)

3-Phenylsulfonyliminochromene (4) (0.01 mol) was heated in a mixture of conc. HCl and ethanol (1:1, 20 mL) for 15 min. The reaction mixture was left to stand at room temperature overnight, and the solid product was filtered and recrystallized from ethanol to give (5).

Preparation of compound (6)

To a stirred suspension of sodium ethoxide (0.23 g, from 0.01 mol sodium and 10 mL ethanol) in DMF (20 mL), phenylsulfonyl acetonitrile (0.01 mol) was added. To the resulting solution the phenyl isothiocyanate (0.01 mol) was added and the reaction mixture stirred for 24 h. at room temperature.

Synthesis of the acyclic intermediates 7, 11, 13 and 15. General procedure

Equimolecular quantities of 6 in ethanol and a α-chloroacetamide and/or chloroacetone and/or chlo-roacetonitrile and/or ethyl bromoacetate were stirred for 6 hr. at room temperature, then left to stand at the same temperature for 24 h. The reaction mixture was washed with water, dried and crystallized from ethanol to give 7, 11, 13 and 15 respectively (cf. Table 1).

Synthesis of thiophene derivatives (10)

A mixture of equimolecular amounts of 6 and phenacyl bromide (0.01 mol) was refluxed in ethanol (20 mL) containing a catalytic amount of TEA for 6 h. The reaction mixture was cooled, filtered and recrystallized from ethanol to give 10 (cf. Table 1).

Synthesis of thiophene derivatives ( 8, 12, 14 and 16 )

Method A

A mixture of equimolecular amounts of 6, and α-halo compounds (0.01 mol) was refluxed in DMF (20 mL) for 6 h. The reaction mixture was cooled, filtered and recrystallized from ethanol to give the corresponding thiophene derivatives. (cf. Table 1).

Method B

Refluxing the acyclic intermediate (7, 11, 13 and/or 15) in ethanol (20 mL) containing a catalytic amount of TEA for 3 h. afforded the corresponding substituted thiophene derivatives 8, 12, 14 and 16 respectively.

References and Notes

  1. Kaliszan, R.; Milczarska, B.; Lega, B. J. Pharmacol. Pharm. 1978, 30(4), 585, (C.A. 1979, 90, 197398y).
  2. Allen, M. P.; Gottlieb, D. Appl. Microbiol. 1970, 20(6), 919.
  3. Fadda, A.A.; Refat, Hala M.; Biehl (Eds.) J. Org. Chem. 1995, 60, 1985.
  4. Fadda, A.A.; Refat, Hala M.; Biehl (Eds.) Heterocycles 1995, 41, 289.
  5. Balasubramanian; et al. J. Chem. Soc. 1955, 3296. Hussien, A.H.; Elghandour, A.H.H.; Ramiz, M.M.M.; Elnagdi, M.H. Synthesis 1989, 775. Dressler, H.; Graham, J. E. J. Org. Chem. 1967, 32(4), 985. [CrossRef]
  6. Fadda, A.A.; Refat, Hala M.; El-Zemaity, M. T.; Biehl (Eds.) Heterocycles 1996, 43, 23.
  7. Fadda, A. A.; Amer, F. A.; Zaki, M. E. A. Phosphorus, Sulfur and Silicon 1999. accepted.
  8. Fadda, A.A.; Refat, Hala M.; Zaki, M. E. A. Synthetic Communications 1999. accepted.
  9. Fadda, A. A.; Abdelrazek, F. M. Z. Naturforsch. 1986, 41b, 499.
  10. Fadda, A.A.; Refat, Hala M. Synthetic Communications 1999. accepted.
  11. Fuentes, L.; Vaquero, J.; Ardid, M. I.; Castillo, J. Del; Soto, L. Jose. Synthesis 1999, 9, 768.
  12. Rao, R. B.; Singh, S. R. J. Indian Chem. Soc. 1973, 50, 492.
  13. Bhargava, P. N.; Sharma, S. C. Bull. Chem. Soc., Jpn. 1962, 35, 1926.
  14. Mallick, S. K.; Martin, A. R.; Lingard, R. G. J. Med. Chem. 1971, 14, 528.
  15. Singh, S. R. J. Indian Chem. Soc. 1975, 52, 734.
  16. Hantzsch, A.; Weber, H. J. Ber. Dtsch. Chem. Ges. 1887, 20, 3118. [CrossRef]
  17. Mehta, M. R.; Teivedi, J. P. Indian J. Chem. Sect. B 1990, 29(12), 1146.
  • Samples Availability: available from the authors.
Table 1. Characterization of the newly prepared compounds.
Table 1. Characterization of the newly prepared compounds.
No.mp° CYld%Mol. formulaAnalysis Calcd. ( Found %)Characterization
CHN
3a18078C19H12N4O4S56.713.1414.71IR: 3350-3450 (NH2), 2220 (CN),
(380.38)(56.84)(3.15)(14.73)1610cm-1 (C=N); 1 H-NMR (CDCl3) δ
6.5 (s, 2H, NH2 exchangeable with
D2O,), 7.8-8.4 (m, 9H, Ar-H), 8.5 (s,
1H, o-Py-H); MS: (m/z) 380 M+.
3b12583C21H19N3O5S59.104.439.87IR: 3350-3450 (NH2), 2220 (CN),
(425.47)(59.29)(4.47)(9.88)1610cm-1 (C=N); 1 H-NMR (CDCl3) δ
3.8 (s, 3H, OCH3), 3.9 (s, 3H, OCH3),
4.0 (s, 3H, OCH3), 7.1 (d, 2H, NH2,
exchangeable with D2O), 7.7-8.0 (m,
6H, Ar-H), 8.5 (s, 1H, o-Py-H); MS:
(m/z) 425 M+ .
422590C19H13NO3S68.003.844.15IR: 3150 (NH), 1650 (C=N), 1561cm-
(335.38)(68.05)(3.88)(4.17)1 (Ph); 1 H-NMR (CDCl3) δ 7.3-8.5
(m, 11H, Ar-H), 8.8 (s, 1H, NH ex-
changeable with D2O), 9.2 (s, 1H, C4-
H); MS: (m/z) 335 M+ .
526798C19H12O4S67.693.56 IR: 1700 (γ-Lactone), 1555cm-1 (Ph);
(336.37)(67.85)(3.57)1 H-NMR (CDCl3) δ 7.55-8.25 (m,
9H, Ar-H), 8.4 (d, J=8.1 Hz, 1H, C9-
H), 8.45 (d, J=8.1 Hz,1H, C10-H), 9.2
(s, 1H, C4-H); MS: (m/z) 336 M+ .
721985C17H15N3O3S254.554.0011.24IR: 3340 (NH2), 3150(NH), 2220
(373.46)(54.69)(4.02)(11.26)(CN), 1680cm-1 (C=O, amidic); 1H-
NMR (CDCl3) δ 3.7(s, 2H, CH2), 6.2
(br, 2H, CONH2 exchangeable with
D2O), 7.2-7.98 (m, 10H, Ar-H), 9.25
(s, 1H, NH exchangeable with D2O);
MS: (m/z) 373 M+ .
814562C17H15N3O3S245.514.0111.23IR: 3450 (NH2), 3150(NH), 1661
(373.46)(45.50)(4.02)(11.26)(CO), 1550 (Ph), 1270, 1180cm-1
(SO2); 1 H-NMR (CDCl3) δ 5.5 (br,
2H, NH2 exchangeable with D2O), 6.2
(br, 2H, CONH2 exchangeable with
D2O), 7.4-8.0 (m, 10H, Ar-H), 8.6 (s,
1H, NH exchangeable with D2O);
MS: (m/z) 373 M+
1015488C23H18N2O3S263.504.126.43IR: 3463 (NH2), 3194(NH), 1720
(434.54)(63.59)(4.14)(6.45)(CO), 1587cm-1 (Ph); 1 H-NMR
(CDCl3) δ 6.5 (br, 2H, NH2 ex-
changeable with D2O), 7.3-8.1 (m,
15H, Ar-H), 9.22 (s, 1H, NH ex-
changeable with D2O); MS: (m/z)
434 M+ .
1119094C18H16N2O3S258.004.297.50IR: 3287(NH), 2220 (CN), 1730
(372.47)(58.06)(4.30)(7.52)(CO), 1603 cm-1 (Ph); 1 H-NMR
(CDCl3) δ 2.3 (s, 3H, CH3), 3.7 (s,
2H, CH2), 7.16-7.97 (m, 10H, Ar-H),
9.25 (s, 1H, NH exchangeable with
D2O); MS: (m/z) 372 M+ .
1216588C18H16N2O3S258.104.287.51IR: 3456 (NH2), 3288 (NH), 1730
(372.47)(58.06)(4.30)(7.52)(CO), 1603cm-1 (Ph); 1 H-NMR
(CDCl3) δ 2.14 (s, 3H, CH3), 5.3 (br,
2H, NH2 exchangeable with D2O),
7.26-7.96 (m, 10H, Ar-H), 9.25 (s,
1H, NH exchangeable with D2O);
MS: (m/z) 372 M+
1318880C17H13N3O2S257.333.6511.82IR: 3200 (NH), 2220, 2195 (two CN),
(355.44)(57.46)(3.66)(11.83)1603 cm-1 (Ph); 1 H-NMR (CDCl3) δ
3.23 (s, 2H, CH2), 7.12-7.87 (m, 10H,
Ar-H), 9.25 (s, 1H, NH exchangeable
with D2O); MS: (m/z) 355M+ .
1415866C17H13N3O2S257.293.6311.81IR: 3456 (NH2), 3266 (NH), 2220
(355.44)(57.46)(3.66)(11.83)(CN), 1603cm-1 (Ph); 1 H-NMR
(CDCl3) δ 6.5 (br, 2H, NH2 ex-
changeable with D2O), 7.31-7.96 (m,
10H, Ar-H), 8.7 (s, 1H, NH ex-
changeable with D2O); MS: (m/z)
355M+ .
1524893C19H18N2O4S256.664.466.95IR: 3278(NH), 2220 (CN), 1730 cm-1
(402.49)(56.71)(4.47)(6.96)(CO); 1 H-NMR (CDCl3) δ 1.3 (t,
J=2.5 Hz, 3H, CH3), 3.7 (s, 2H, CH2),
4.3 (q, J=2.5Hz, 2H, CH2), 7.5-8.56
(m, 10H, Ar-H), 9.25 (s, 1H, NH ex-
changeable with D2O); MS: (m/z)
402 M+ .
1615286C19H18N2O4S256.704.456.94IR: 3448 (NH2), 3243(NH), 1730
(402.50)(56.71)(4.47)(6.96)(CO), 1603cm-1 (Ph); 1 H-NMR
(CDCl3) δ 1.26 (t, J= 2.5 Hz, 3H,
CH3), 4.22 (q, J=2.5Hz, 2H, CH2),
6.55 (br, 2H, NH2 exchangeable with
D2O), 7.18-7.96 (m, 10H, Ar-H), 9.25
(s, 1H, NH exchangeable with D2O);
MS: (m/z) 402 M+ .

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MDPI and ACS Style

Fadda, A.A.; Refat, H.M.; Zaki, M.E.A. Utility of Sulphones in Heterocyclic Synthesis: Synthesis of Some Pyridine, Chromene and Thiophene Derivatives. Molecules 2000, 5, 701-709. https://doi.org/10.3390/50500701

AMA Style

Fadda AA, Refat HM, Zaki MEA. Utility of Sulphones in Heterocyclic Synthesis: Synthesis of Some Pyridine, Chromene and Thiophene Derivatives. Molecules. 2000; 5(5):701-709. https://doi.org/10.3390/50500701

Chicago/Turabian Style

Fadda, A. A., Hala M. Refat, and M. E. A. Zaki. 2000. "Utility of Sulphones in Heterocyclic Synthesis: Synthesis of Some Pyridine, Chromene and Thiophene Derivatives" Molecules 5, no. 5: 701-709. https://doi.org/10.3390/50500701

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