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