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6-Methoxynicotinic acid

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6-Methoxynicotinic acid Basic information

Product Name:
6-Methoxynicotinic acid
Synonyms:
  • 6-Methoxypyridine-3-carboxylic acid, 5-Carboxy-2-methoxypyridine, 2-Methoxypyridine-5-carboxylic acid
  • 6-methoxy-3-pyridinecarboxylic acid
  • 6-methoxy-3-pyridinecarboxylate
  • RARECHEM AL BO 0733
  • 2-METHOXYPYRIDINE-5-CARBOXYLIC ACID
  • 2-METHOXY-5-PYRIDINECARBOXYLIC ACID
  • 6-METHOXYNICOTINIC ACID
  • 6-Methoxypyridine-3-carboxylic acid
CAS:
66572-55-2
MF:
C7H7NO3
MW:
153.14
Product Categories:
  • Heterocycle-Pyridine series
  • Acids & Esters
  • Anisoles, Alkyloxy Compounds & Phenylacetates
  • Carboxylic Acids
  • Pyridines
  • Building Blocks
  • Pyridine
Mol File:
66572-55-2.mol
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6-Methoxynicotinic acid Chemical Properties

Melting point:
171.5-172.5 °C(Solv: water (7732-18-5))
Boiling point:
283.8±20.0 °C(Predicted)
Density 
1.284
storage temp. 
Sealed in dry,Room Temperature
form 
solid
pka
3.74±0.10(Predicted)
color 
Light yellow
CAS DataBase Reference
66572-55-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2933399990
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6-Methoxynicotinic acid Usage And Synthesis

Uses

2-Methoxy-5-pyridinecarboxylic Acid is used in the synthesis of caudatin derivatives as anti-hepatitis B virus agents. In addition it can be used the synthesize potent, selective GSK-3 inhibitors for the use in the treatment of various ailments.

Definition

ChEBI: 6-Methoxy-pyridine-3-carboxylic acid is an aromatic carboxylic acid and a member of pyridines.

Synthesis

26218-80-4

66572-55-2

General procedure for the synthesis of 6-methoxynicotinic acid from methyl 6-methoxynicotinate: sodium hydroxide (0.36 g, 9.0 mmol) was dissolved in a solvent mixture of methanol (5 mL) and water (5 mL). To this solution was added methyl 6-methoxynicotinate (1.00 g, 5.98 mmol), followed by stirring the reaction mixture at 70 °C for 90 minutes. After completion of the reaction, the solution was cooled to room temperature and diluted with 1N sodium hydroxide solution (25 mL). The diluted solution was extracted with ethyl acetate and the aqueous layer was isolated. The aqueous layer was acidified to pH 1 with hydrochloric acid and subsequently extracted three times with ethyl acetate. All organic layers were combined, dried with anhydrous sodium sulfate and concentrated under reduced pressure to give 6-methoxynicotinic acid as a white solid (0.849 g, 92% yield). Mass spectrometry analysis (APCI positive ion mode) showed m/z 154.1 (100%) (M + H).

References

[1] Patent: WO2008/11131, 2008, A2. Location in patent: Page/Page column 138-139
[2] Patent: EP1621537, 2006, A1. Location in patent: Page/Page column 42
[3] Patent: EP1762568, 2007, A1. Location in patent: Page/Page column 40-41
[4] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1988, p. 227 - 234
[5] Patent: US2003/100576, 2003, A1

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