ChemicalBook--->CAS DataBase List--->30062-34-1

30062-34-1

30062-34-1 Structure

30062-34-1 Structure
IdentificationBack Directory
[Name]

Methyl 6-oxo-1,6-dihydropyridine-2-carboxylate
[CAS]

30062-34-1
[Synonyms]

methyl 6-hydroxypicolinate
6-Methoxycarbonyl-2-pyridone
methyl 6-oxo-1H-pyridine-2-carboxylate
methyl 6-hydroxypicolinate hydrochloride
Methyl 6-oxo-1,6-dihydropyridine-2-carboxylate
2-Pyridinecarboxylic acid, 1,6-dihydro-6-oxo-, methyl ester
[Molecular Formula]

C7H7NO3
[MDL Number]

MFCD17015470
[MOL File]

30062-34-1.mol
[Molecular Weight]

153.14
Chemical PropertiesBack Directory
[Melting point ]

109-110 °C
[Boiling point ]

367.6±42.0 °C(Predicted)
[density ]

1.263±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

8.83±0.10(Predicted)
[Appearance]

White to off-white Solid
[InChI]

InChI=1S/C7H7NO3/c1-11-7(10)5-3-2-4-6(9)8-5/h2-4H,1H3,(H,8,9)
[InChIKey]

GJLWQAUHCDNAEK-UHFFFAOYSA-N
[SMILES]

C1(C(OC)=O)NC(=O)C=CC=1
Questions And AnswerBack Directory
[Uses]

Methyl 6-oxo-1,6-dihydropyridine-2-carboxylate, as an important pharmaceutical intermediate and fine chemical raw material, has a wide range of applications and a broad market prospect. In the pharmaceutical field, 2-pyridinemethanol, as an important pharmaceutical intermediate, can be used to synthesize bisacodyl, a blood transfusion drug, and is also a raw material for synthesizing pralidoxime, an organophosphate antidote.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H317
[Precautionary statements ]

P501-P261-P272-P280-P302+P352-P362+P364-P333+P313
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 6-oxo-1,6-dihydropyridine-2-carboxylate(30062-34-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methanol

67-56-1

6-Hydroxypicolinic acid

19621-92-2

Methyl 6-oxo-1,6-dihydropyridine-2-carboxylate

30062-34-1

Step 1: Synthesis of methyl 6-hydroxypyridine-2-carboxylate. 6-Hydroxypyridine-2-carboxylic acid (13.0 g, 93.5 mmol) was dissolved in methanol (150 mL) at room temperature and a dioxane solution of 4N HCl (10 mL) was slowly added. The reaction mixture was stirred at room temperature for 48 hours. Upon completion of the reaction, the solvent was removed by concentration under reduced pressure to afford methyl 6-hydroxypyridine-2-carboxylate (13 g, 90% yield) as a white solid.

[References]

[1] Patent: WO2004/37808, 2004, A1. Location in patent: Page 19-20
[2] Patent: WO2014/154727, 2014, A1. Location in patent: Page/Page column 38; 52
[3] Patent: US2014/296239, 2014, A1. Location in patent: Paragraph 0097; 0098
[4] Patent: WO2014/154726, 2014, A1. Location in patent: Page/Page column 38-39
[5] Patent: US2014/296296, 2014, A1. Location in patent: Paragraph 0106; 0107
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