Basic information Safety Supplier Related

7-BROMO-4-OXO-1,4-DIHYDRO-QUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER

Basic information Safety Supplier Related

7-BROMO-4-OXO-1,4-DIHYDRO-QUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER Basic information

Product Name:
7-BROMO-4-OXO-1,4-DIHYDRO-QUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER
Synonyms:
  • 7-BROMO-4-OXO-1,4-DIHYDRO-QUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER
  • Ethyl 7-bromo-4-hydroxyquinoline-3-carboxylate
  • Ethyl 4-hydroxy-7-broMoquinoline-3-carboxylate
  • Ethyl7-BroMo-4-hydroxy-3-quinolinecarboxylate
  • 7-bromo-4-hydroxyquinoline-3-carboxylate
  • 3-Quinolinecarboxylic acid, 7-bromo-4-hydroxy-, ethyl ester
  • 3-Quinolinecarboxylicacid, 7-bromo-4-hydroxy-, ethy..
  • ethyl 7-bromo-1,4-dihydro-4-oxo-3-quinolinecarboxylate, 95%
CAS:
179943-57-8
MF:
C12H10BrNO3
MW:
296.12
Mol File:
179943-57-8.mol
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7-BROMO-4-OXO-1,4-DIHYDRO-QUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER Chemical Properties

Melting point:
307-309 °C
Boiling point:
385.5±37.0 °C(Predicted)
Density 
1.593±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
pka
2.16±0.50(Predicted)
Appearance
White to off-white Solid
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Safety Information

HS Code 
2933499090
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7-BROMO-4-OXO-1,4-DIHYDRO-QUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER Usage And Synthesis

Synthesis

351893-47-5

208580-23-8

Dowtherm (50 mL) was added to a 100 mL two-necked round-bottomed flask and heated to 250 °C in a sand bath. Maintaining this temperature, diethyl {[(3-bromophenyl)amino]methylene}malonate (Intermediate 32, 10.0 g, 29.2 mmol) was added to the reaction system and the reaction was continued at 250 °C for 1 hour. After completion of the reaction, the reaction mixture was cooled to room temperature and a white solid was collected by filtration and dried to give ethyl 7-bromo-4-oxo-1,4-dihydroquinoline-3-carboxylate 6.0 g in 69.3% yield. The product was characterized by 1H NMR (400 MHz, DMSO-d6): δ 1.07 (t, 3H), 1.22 (s, 12H), 3.16 (q, 2H), 7.29 (m, 1H), 7.31 (d, 2H), 7.61 (s, 1H), 7.88 (s, 1H), 8.31 (s, 1H), 8.65 (s, 1H), and 9.44 (s, 1H).

References

[1] Journal of Medicinal Chemistry, 2015, vol. 58, # 14, p. 5522 - 5537
[2] Patent: WO2009/147433, 2009, A1. Location in patent: Page/Page column 279
[3] Bioorganic and Medicinal Chemistry, 2012, vol. 20, # 15, p. 4790 - 4800
[4] Bioorganic and Medicinal Chemistry Letters, 2006, vol. 16, # 4, p. 1010 - 1013
[5] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 15, p. 5055 - 5058

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