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ETHYL 4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLATE

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ETHYL 4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLATE Basic information

Product Name:
ETHYL 4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLATE
Synonyms:
  • ETHYL 4-HYDROXY-6-METHOXY-3-QUINOLINECARBOXYLATE
  • ETHYL 4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLATE
  • BUTTPARK 20\09-61
  • 4-HYDROXY-6-METHOXY-QUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER
  • 4-Hydroxy-6-methoxy-3-quinolinecarboxylic acid ethyl ester
  • 4-keto-6-methoxy-1H-quinoline-3-carboxylic acid ethyl ester
  • ethyl 6-methoxy-4-oxo-1H-quinoline-3-carboxylate
  • Ethyl 4-hydroxy-6-(methyloxy)-3-quinolinecarboxylate
CAS:
77156-78-6
MF:
C13H13NO4
MW:
247.25
EINECS:
804-439-6
Product Categories:
  • blocks
  • Carboxes
  • Quinolines
Mol File:
77156-78-6.mol
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ETHYL 4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLATE Chemical Properties

Melting point:
280-283℃
Boiling point:
373.2±37.0 °C(Predicted)
Density 
1.277
storage temp. 
Sealed in dry,Room Temperature
pka
2.72±0.50(Predicted)
Appearance
Light brown to brown Solid
InChI
InChI=1S/C13H13NO4/c1-3-18-13(16)10-7-14-11-5-4-8(17-2)6-9(11)12(10)15/h4-7H,3H2,1-2H3,(H,14,15)
InChIKey
VNGGYIBIGOOVNP-UHFFFAOYSA-N
SMILES
N1C2C(=CC(OC)=CC=2)C(O)=C(C(OCC)=O)C=1
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36
Safety Statements 
26
WGK Germany 
3
HS Code 
2933499090
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ETHYL 4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLATE Usage And Synthesis

Synthesis

83507-70-4

77156-78-6

A solution was prepared from diethyl 2-[(4-methoxyanilino)methylene]malonate (CAS: 83507-70-4, 71.4 g, 0.24 mol) in 150 mL of diphenyl ether. The reaction system was placed in a metal bath and slowly heated to 243 °C and maintained at this temperature for 3 hours. During the reaction, 15 mL of liquid was distilled. Upon completion of the reaction, the mixture was cooled to room temperature and subsequently dissolved by adding 250 mL of hexane. After stirring the mixture for 3 hours, a filtration operation was performed. The resulting solid was washed with hexane and dried to give ethyl 4-hydroxy-6-methoxyquinoline-3-carboxylate (25.0 g, 0.10 mol, 41% yield), the purity of which meets the requirements for direct use in subsequent reactions. The structure of the product was confirmed by 1H-NMR (CDCl3) and LC-MS: 1H-NMR (CDCl3) δ= 1.28 (t, 3H), 3.85 (s, 3H), 4.21 (q, 2H), 7.34 (dd, 1H), 7.55-7.62 (m, 2H), 8.49 (s, 1H); LC-MS: Rt = 1.17 min ; MS: m/z = 248 [M + 1]+.

References

[1] Patent: WO2006/2047, 2006, A2. Location in patent: Page/Page column 60
[2] European Journal of Medicinal Chemistry, 2015, vol. 103, p. 1 - 16
[3] Organic Process Research and Development, 2014, vol. 18, # 11, p. 1482 - 1491
[4] Tetrahedron Letters, 2017, vol. 58, # 8, p. 794 - 796
[5] Journal of the American Chemical Society, 1946, vol. 68, p. 1204,1206

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