Basic information Safety Supplier Related

1H-Pyrrolo[2,3-b]pyridine, 1-(phenylsulfonyl)-

Basic information Safety Supplier Related

1H-Pyrrolo[2,3-b]pyridine, 1-(phenylsulfonyl)- Basic information

Product Name:
1H-Pyrrolo[2,3-b]pyridine, 1-(phenylsulfonyl)-
Synonyms:
  • 1-(Phenylsulphonyl)-7-azaindole
  • N-Benzenesulfonyl-7-azaindole
  • 1-(benzenesulfonyl)-1H-pyrrolo[2,3-b]pyridine
  • 1-(Benzenesulfonyl)pyrrolo[2,3-b]pyridine
  • 1H-Pyrrolo[2,3-b]pyridine, 1-(phenylsulfonyl)-
  • 1-(Phenylsulfonyl)-7-azaindole
CAS:
143141-23-5
MF:
C13H10N2O2S
MW:
258.3
Product Categories:
  • Heterocycle-Pyridine series
Mol File:
143141-23-5.mol
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1H-Pyrrolo[2,3-b]pyridine, 1-(phenylsulfonyl)- Chemical Properties

Melting point:
130-132 °C
Boiling point:
465.8±37.0 °C(Predicted)
Density 
1.34±0.1 g/cm3(Predicted)
storage temp. 
Store at 0-8 °C
pka
1.38±0.30(Predicted)
Appearance
brown solid
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
HS Code 
2933998090
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1H-Pyrrolo[2,3-b]pyridine, 1-(phenylsulfonyl)- Usage And Synthesis

Synthesis

271-63-6

98-09-9

143141-23-5

4.2.4 Synthesis of 1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine (5) In a dry and nitrogen purged round bottom flask, 1H-pyrrolo[2,3-b]pyridine (1.01 g, 8.58 mmol), tetrabutylammonium bromide (81 mg, 0.25 mmol), finely ground sodium hydroxide (1.02 g, 25.41 mmol) and dichloromethane (20 mL) were added. The mixture was cooled to 0 °C in an ice bath and stirred, followed by the slow dropwise addition of benzenesulfonyl chloride (1.35 mL, 10.59 mmol). The reaction mixture was gradually warmed to room temperature and stirred continuously at this temperature for 1 hour. Upon completion of the reaction, water (20 mL) was added for hydrolysis and then extracted twice with dichloromethane. The organic layers were combined, washed with saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give 2.38 g of a beige solid. The crude product was purified by silica gel column chromatography (eluent: cyclohexane/ethyl acetate=7:3) to give 2.17 g of white solid target product in 99% yield. 1H NMR (300 MHz, CDCl3) δ (ppm): 8.45 (dd, J = 1.5, 4.8 Hz, 1H), 8.20 (d, J = 7.5 Hz, 2H), 7.86 (dd, J = 1.5, 7.8 Hz, 1H), 7.73 (d, J = 4.0 Hz, 1H), 7.57 (dd, J = 7.4 Hz, 1H ), 7.52-7.47 (m, 2H), 7.19 (dd, J = 4.8, 7.8 Hz, 1H), 6.61 (d, J = 4.0 Hz, 1H). 13C NMR (75 MHz, CDCl3) δ (ppm): 144.7 (2C), 138.3, 134.1, 129.9, 129.1 (2C), 128.0 (2C), 126.5, 123.0, 119.0, 105.5.

References

[1] European Journal of Medicinal Chemistry, 2016, vol. 108, p. 701 - 719
[2] Patent: WO2016/114816, 2016, A1. Location in patent: Paragraph 0290
[3] Organic Letters, 2015, vol. 17, # 19, p. 4710 - 4713
[4] Tetrahedron, 1997, vol. 53, # 10, p. 3637 - 3648
[5] Patent: WO2006/50076, 2006, A1. Location in patent: Page/Page column 61

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