Basic information Safety Supplier Related

4-BROMO-1-[(4-METHYLPHENYL)SULFONYL]-1H-PYRROLO[2,3-B]PYRIDINE

Basic information Safety Supplier Related

4-BROMO-1-[(4-METHYLPHENYL)SULFONYL]-1H-PYRROLO[2,3-B]PYRIDINE Basic information

Product Name:
4-BROMO-1-[(4-METHYLPHENYL)SULFONYL]-1H-PYRROLO[2,3-B]PYRIDINE
Synonyms:
  • 4-BROMO-1-[(4-METHYLPHENYL)SULFONYL]-1H-PYRROLO[2,3-B]PYRIDINE
  • 1H-Pyrrolo[2,3-b]pyridine, 4-bromo-1-[(4-methylphenyl)sulfonyl]-
  • N-Tosyl-4-bromo-7-azaindole
  • 4-Bormo-1-tosyl-7-azaindole
  • 4-Bromo-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridine
  • 4-Bromo-1-tosyl-1H-pyrrolo[2,3-b]pyridine
  • 4-Bromo-1-tosyl-7-azaindo...
  • 4-BroMo-1-tosyl-7-azaindole
CAS:
348640-07-3
MF:
C14H11BrN2O2S
MW:
351.22
Product Categories:
  • Heterocycle-Pyridine series
Mol File:
348640-07-3.mol
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4-BROMO-1-[(4-METHYLPHENYL)SULFONYL]-1H-PYRROLO[2,3-B]PYRIDINE Chemical Properties

Boiling point:
514.9±60.0 °C(Predicted)
Density 
1.59±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
2.14±0.30(Predicted)
Appearance
Off-white to yellow Solid
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Safety Information

RIDADR 
UN2811
HS Code 
2933998090
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4-BROMO-1-[(4-METHYLPHENYL)SULFONYL]-1H-PYRROLO[2,3-B]PYRIDINE Usage And Synthesis

Synthesis

98-59-9

348640-06-2

348640-07-3

4-Bromo-7-azaindole (3 g, 15.22 mmol) was used as starting material and dissolved in tetrahydrofuran (THF, 50 mL) under nitrogen protection in a round bottom flask. The reaction mixture was cooled to 0 °C and sodium hydride (60% dispersed in mineral oil, 0.67 g, 16.75 mmol) was added in batches, and the outgassing phenomenon was observed during the addition. After the addition, the reaction mixture was stirred at room temperature for 30 min. Subsequently, p-toluenesulfonyl chloride (2.14 mL, 16.75 mmol) was slowly added to the reaction system. The reaction mixture was gradually warmed up to room temperature and stirring was continued for 2 hours. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure and the residue was dissolved with dichloromethane (DCM, 30 mL). The organic phase was washed with 2 M sodium carbonate solution (2 x 30 mL), dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated to give an orange colored oil. Purification was carried out by fast column chromatography with the eluent ethyl acetate:cyclohexane (1:9, v/v) to afford the target compound 4-bromo-1-[(4-methylphenyl)sulfonyl]-1H-pyrrolo[2,3-B]pyridine as an off-white solid in 92% yield. The product was analyzed by LCMS (Method 5, retention time 5.36 min, molecular ion peak m/z 337 [M + H]+) and 1H NMR (500 MHz, CDCl3) to confirm the structure: δ 8.22 (d, 1H), 8.18 (d, 2H), 7.78 (d, 1H), 7.58 (t, 1H), 7.48 (t, 2H), 7.35 (d , 1H), 6.63 (d, 1H).

References

[1] Tetrahedron Letters, 2016, vol. 57, # 42, p. 4718 - 4722
[2] Patent: US2015/274720, 2015, A1. Location in patent: Paragraph 0202
[3] Patent: US2011/306613, 2011, A1. Location in patent: Page/Page column 23
[4] Patent: WO2008/145688, 2008, A2. Location in patent: Page/Page column 42; 89
[5] Patent: WO2007/76320, 2007, A2. Location in patent: Page/Page column 34-35

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