Basic information Safety Supplier Related

6-bromo-4-chlorocinnoline

Basic information Safety Supplier Related

6-bromo-4-chlorocinnoline Basic information

Product Name:
6-bromo-4-chlorocinnoline
Synonyms:
  • 6-bromo-4-chlorocinnoline
  • Cinnoline, 6-broMo-4-chloro-
  • 6-bromo-4-chlorocinnoline - [B24879]
CAS:
68211-15-4
MF:
C8H4BrClN2
MW:
243.49
Mol File:
68211-15-4.mol
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6-bromo-4-chlorocinnoline Chemical Properties

Melting point:
127-128℃
Boiling point:
359.6±45.0 °C(Predicted)
Density 
1.762
storage temp. 
Storage temp. -20°C
pka
-1.08±0.10(Predicted)
Appearance
Light yellow to light brown Solid
InChI
InChI=1S/C8H4BrClN2/c9-5-1-2-8-6(3-5)7(10)4-11-12-8/h1-4H
InChIKey
WAKDQKOZUBTOEX-UHFFFAOYSA-N
SMILES
N1=C2C(C=C(Br)C=C2)=C(Cl)C=N1
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6-bromo-4-chlorocinnoline Usage And Synthesis

Synthesis

876-88-0

68211-15-4

General procedure for the synthesis of 4-chloro-6-bromocinnoline from 6-bromocinnolin-4-ol: Thionyl chloride (3 mL) and N,N-dimethylformamide (30 μL) were sequentially added to 6-bromoquinolin-4(1H)-one (300 mg, 1.33 mmol), and the reaction mixture was heated to reflux for 30 min. After completion of the reaction, the reaction solution was concentrated under reduced pressure and saturated aqueous sodium bicarbonate was added to the residue and extracted with ethyl acetate. The organic layers were combined, washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and distilled under reduced pressure to remove the solvent. The resulting crude product was purified by silica gel column chromatography (eluent: hexane/ethyl acetate) to afford 4-chloro-6-bromocinnoline (288 mg, 89% yield) as a yellow solid.

References

[1] Patent: JP6378918, 2018, B2. Location in patent: Paragraph 0721; 0724
[2] Patent: US2015/259331, 2015, A1. Location in patent: Paragraph 0192
[3] Bioorganic and Medicinal Chemistry, 2006, vol. 14, # 20, p. 6832 - 6846
[4] Patent: US2003/187026, 2003, A1
[5] Journal of the Chemical Society, 1950, p. 384,389

6-bromo-4-chlorocinnolineSupplier

Xi'an Jurenhexin Pharmaceutical Technology Co., Ltd Gold
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029-86518151 13629269978
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Zaozhuang Benefit Chemical Co., Ltd. Gold
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0531-69958783 15508681609
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Capot Chemical Co., Ltd
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+86 (0) 571 85 58 67 18
Shanghai Ennopharm Co., Ltd.
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+86 (21) 6435-5022
China Langchem Inc.
Tel
0086-21-58956006
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