4-Hydroxy-6-methoxyquinoline-3-carboxylic acid

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4-Hydroxy-6-methoxyquinoline-3-carboxylic acid Basic information
Product Name:4-Hydroxy-6-methoxyquinoline-3-carboxylic acid
Synonyms:BUTTPARK 20\09-62;3-CARBOXY-4-HYDROXY-6-METHOXYQUINOLINE;AKOS BB-8879;4-hydroxy-6-methoxy-3-quinoline carboxylic acid;Nsc80675;6-methoxy-4-oxo-1H-quinoline-3-carboxylic acid;3-Quinolinecarboxylic acid, 4-hydroxy-6-methoxy-;4-Hydroxy-6-methoxyquinoline-3-carboxylic acid
CAS:28027-16-9
MF:C11H9NO4
MW:219.19
EINECS:
Product Categories:pharmacetical
Mol File:28027-16-9.mol
4-Hydroxy-6-methoxyquinoline-3-carboxylic acid Structure
4-Hydroxy-6-methoxyquinoline-3-carboxylic acid Chemical Properties
Melting point 278-279 °C (decomp)
Boiling point 418.6±45.0 °C(Predicted)
density 1.444±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
form solid
pka0.74±0.30(Predicted)
AppearanceOff-white to light yellow Solid
InChI1S/C11H9NO4/c1-16-6-2-3-9-7(4-6)10(13)8(5-12-9)11(14)15/h2-5H,1H3,(H,12,13)(H,14,15)
InChIKeyYUXLPEGMXYHPCZ-UHFFFAOYSA-N
SMILESO=C(O)C1=C(O)C2=C(C=CC(OC)=C2)N=C1
CAS DataBase Reference28027-16-9(CAS DataBase Reference)
Safety Information
WGK Germany WGK 3
HS Code 2933499090
Storage Class11 - Combustible Solids
MSDS Information
4-Hydroxy-6-methoxyquinoline-3-carboxylic acid Usage And Synthesis
Synthesis
ETHYL 4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLATE

77156-78-6

4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLIC ACID

28027-16-9

General procedure for the synthesis of 4-hydroxy-6-methoxyquinoline-3-carboxylic acid from ethyl 4-hydroxy-6-methoxyquinoline-3-carboxylate: ethyl 4-hydroxy-6-methoxyquinoline-3-carboxylate (17.8 g, 72 mmol) was suspended in 170 mL of aqueous 2 N sodium hydroxide solution, heated to 90 °C, and the reaction was maintained for 1.5 h. The mixture was cooled to room temperature and slowly poured into ice water. Upon completion of the reaction, the mixture was cooled to room temperature, slowly poured into ice water and the pH was adjusted to 5 with 2 N hydrochloric acid.The precipitated solid was collected by filtration, washed with cold water and dried to give 4-hydroxy-6-methoxyquinoline-3-carboxylic acid (15.8 g, 72 mmol, 99% yield). The product was characterized by 1H-NMR (DMSO-d6): δ= 3.91 (s, 3H), 7.53 (dd, 1H), 7.64 (d, 1H), 7.82 (d, 1H), 8.80 (d, 1H), 13.63 (bs, 1H), 15.55 (s, 1H).Results of LC-MS analysis: retention time (Rt) = 1.20 min; Mass spectrum (MS): m/z = 220 [M+H]+.

References[1] Tetrahedron Letters, 2017, vol. 58, # 8, p. 794 - 796
[2] Journal of the American Chemical Society, 1946, vol. 68, p. 1204,1206
[3] Organic Syntheses, 1955, vol. Coll. Vol. III, p. 272
[4] Journal of the American Chemical Society, 1947, vol. 69, p. 1659,1660
[5] Journal of the Chemical Society, 1946, p. 1033,1035
4-Hydroxy-6-methoxyquinoline-3-carboxylic acid Preparation Products And Raw materials
Raw materialsEthyl 4-hydroxy-6-methoxyquinoline-3-carboxylate-->Water-->Sodium hydroxide
Preparation Products4-Chloro-6-methoxyquinoline
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