3-Amino-6-ethoxy-4-phenyl-1H-pyrrolo[2,3-b]pyridine-2,5-dicarbonitrile

Panayiotis A. Koutentis; Sophia S. Michaelidou

doi:10.3390/M691

and

Department of Chemistry, University of Cyprus, P.O. Box 20537, 1678 Nicosia, Cyprus

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Author to whom correspondence should be addressed.

Molbank2010, 2010(3), M691;https://doi.org/10.3390/M691

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Abstract

(Z)-2-(4-Chloro-5H-1,2,3-dithiazol-5-ylideneamino)-6-ethoxy-4-phenylpyridine-3,5-dicarbonitrile 1, when treated with either triphenylphosphine (4 equiv.) or polymer bound triphenylphosphine (5 equiv.) in dichloromethane at room temperature for 3 days affords 3‑amino-6-ethoxy-4-phenyl-1H-pyrrolo[2,3-b]pyridine-2,5-dicarbonitrile 2 in 60–62% yields.

Keywords:

pyridine; dithiazole; dithiazolimine; azaindole; indole; heterocycle; polymer bound; solid support

Neutral 1,2,3-dithiazoles, readily prepared from 4,5-dichloro-1,2,3-dithiazolium chloride 2 commonly known as Appel’s salt [], are useful precursors to often difficult to access cyano substituted heteroarenes [,,,]. Recently, we demonstrated the unexpected conversion of 2-(4-chloro-5H-1,2,3-dithiazolylideneamino)benzonitriles into 3-aminoindole-2-carbonitriles using triphenyl-phosphine [].

During this study, we treated (Z)-2-(4-chloro-5H-1,2,3-dithiazol-5-ylideneamino)-6-ethoxy-4-phenylpyridine-3,5-dicarbonitrile 1 [] with triphenylphosphine (4 equiv.) in dichloromethane at room temperature for 3 days and obtained some triphenylphosphine sulfide (93%) and 3‑amino-6-ethoxy-4-phenyl-1H-pyrrolo[2,3-b]pyridine-2,5-dicarbonitrile 2 in 60% yield. By using polymer bound triphenylphosphine (5 equiv.), the chromatographic separation of the triphenylphosphine sulfide could be avoided and the desired pyrrolo[2,3-b]pyridine was isolated by simple filtration in 62% yield.

Experimental

Anhydrous Na₂SO₄ was used for drying organic extracts and volatiles were removed under reduced pressure. The reaction mixture and column eluents were monitored by TLC, using commercial glass backed thin layer chromatography (TLC) plates (Merck Kieselgel 60 F₂₅₄). The plates were observed under UV light at 254 and 365 nm. The technique of dry flash chromatography was used, using Merck Silica Gel 60 (less than 0.063 mm). Melting point was determined using a PolyTherm-A, Wagner & Munz, Kofler-Hotstage Microscope apparatus. IR spectrum was recorded on a Shimadzu FTIR-NIR Prestige-21 spectrometer with Pike Miracle Ge ATR accessory and strong, medium and weak peaks are represented by s, m and w, respectively. ¹H NMR spectrum was recorded on a Bruker Avance 300 machine (at 300 MHz). Deuterated chloroform was used for deuterium lock and the signals are referenced to the residual undeuterated solvent peak. Low resolution (EI) mass spectrum was recorded on a Shimadzu Q2010 GCMS with a direct inlet probe. Microanalysis was performed at London Metropolitan University.

3-Amino-6-ethoxy-4-phenyl-1H-pyrrolo[2,3-b]pyridine-2,5-dicarbonitrile (2)

(a) Using free triphenylphosphine. To a stirred solution of (Z)-2-(4-chloro-5H-1,2,3-dithiazol-5-ylideneamino)-6-ethoxy-4-phenylpyridine-3,5-dicarbonitrile 1 (100 mg, 0.25 mmol) in DCM (4 mL) at ca. 20 °C and protected with a CaCl₂ drying tube, was added triphenylphosphine (262 mg, 1 mmol, 4 equiv.). The mixture was then allowed to stir at ca. 20 °C for 3 days, until no starting materials remained (TLC). The reaction mixture was then adsorbed onto silica and chromatography (hexane/DCM, 5:5) gave triphenylphosphine sulfide (136.7 mg, 93%) as white needles, mp 161–162 °C (from cyclohexane), identical to an authentic sample. Further elusion (hexane/DCM, 2:8) gave the title compound 2 (45.5 mg, 60%) as yellow prisms, mp 191–192 °C (from cyclohexane/EtOH); (Found: C, 67.2; H, 4.4; N, 23.0. C₁₇H₁₃N₅O requires C, 67.3; H, 4.3; N, 23.1%); λ_max (DCM)/nm 243 (log ε 3.21), 276 (3.46), 314 inf (2.80), 328 (2.93), 372 inf (3.39); v_max/cm^-1 3345m (NH), 3231m (NH₂), 2234m (C≡N), 2203s (C≡N), 1587s, 1580s, 1516m, 1489m, 1472m, 1381s, 1315s, 1180m, 1159m, 1024m, 924m, 868m, 793m, 772m, 741s, 702s; δ_H (300 MHz; CDCl₃) 8.31 (1H, br s, NH), 7.59–7.56 (3H, m, Ph H), 7.52–7.48 (2H, m, Ph H), 4.51 (2H, q, J 7.1, CH₂), 3.74 (2H, br s, NH₂), 1.47 (3H, t, J 7.1, CH₃); δ_C (75 MHz, CDCl₃) 163.7, 152.6, 146.0, 138.2, 133.1, 130.4 (Ph CH), 129.2 (Ph CH), 128.3 (Ph CH), 115.2 (C≡N), 113.8 (C≡N), 103.1, 91.2, 87.2, 63.8 (CH₂), 14.3 (CH₃); m/z (EI) 303 (M⁺, 84%), 275 (100), 247 (11), 219 (12), 194 (9), 165 (12), 140 (70), 51 (5).

(b) Using polymer bound triphenylphosphine. To a stirred solution of (Z)-2-(4-chloro-5H-1,2,3-dithiazol-5-ylideneamino)-6-ethoxy-4-phenylpyridine-3,5-dicarbonitrile 1 (100 mg, 0.25 mmol) in DCM (4 mL) at ca. 20 °C and protected with a CaCl₂ drying tube, was added triphenylphosphine polymer bound (328 mg, 1.25 mmol, 5 equiv.). The mixture was then allowed to stir at ca. 20 °C for 3 days, until no starting materials remained (TLC). Filtration of the reaction to remove the polymer, gave 3‑amino-6-ethoxy-4-phenyl-1H-pyrrolo[2,3-b]pyridine-2,5-dicarbonitrile (2) (47 mg, 62%) as yellow prisms mp 191–192 °C (from cyclohexane/EtOH).

Supplementary materials

Supplementary File 1Supplementary File 2Supplementary File 3

Acknowledgements

The authors wish to thank the Cyprus Research Promotion Foundation [Grant No. ΤΕΧΝΟΛΟΓΙΑ/ΘΕΠΙΣ/0308(ΒΕ)/08] and the following organisations in Cyprus for generous donations of chemicals and glassware: the State General Laboratory, the Agricultural Research Institute and the Ministry of Agriculture. Furthermore we thank the A.G. Leventis Foundation for helping to establish the NMR facility in the University of Cyprus.

References and Notes

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