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ChemicalBook--->CAS DataBase List--->30766-22-4

30766-22-4

30766-22-4 Structure

30766-22-4 Structure
IdentificationBack Directory
[Name]

Methyl 5-hydroxynicotinate
[CAS]

30766-22-4
[Synonyms]

METHYL 5-HYDROXYNICOTINATE
5- hydroxyMethyl nicotinate
Methyl 5-hydroxynicotinate 98%
Hydroxynicotinicacidmethylester
METHYL 5-HYDROXYNICOTINATE, 97+%
5-HYDROXYNICOTINIC ACID METHYL ESTER
METHYL 5-HYDROXY-3-PYRIDINECARBOXYLATE
Methyl 5-hydroxypyridine-3-carboxylate
Methyl 5-hydroxynicotinate methy ester
Methyl 5-hydroxynicotinate methyl ester
5-HYDROXYNICOTINIC ACID METHYL ESTER 98+%
5-HYDROXY-3-PYRIDINECARBOXYLIC ACID METHYL ESTER
3-Hydroxy-5-pyridinecarboxylic acid methyl ester
5-Hydroxypyridine-3-carboxylic acid methyl ester
Methyl 5-hydroxypyridine-3-carboxylate, 3-Hydroxy-5-(methoxycarbonyl)pyridine
5-Hydroxynicotinic Acid Methyl Ester 5-Hydroxy-3-pyridinecarboxylic Acid Methyl Ester Methyl 5-Hydroxy-3-pyridinecarboxylate
[Molecular Formula]

C7H7NO3
[MDL Number]

MFCD00191521
[MOL File]

30766-22-4.mol
[Molecular Weight]

153.14
Chemical PropertiesBack Directory
[Appearance]

Light beige powder and lumps
[Melting point ]

190 °C
[Boiling point ]

374.2±22.0 °C(Predicted)
[density ]

1.287±0.06 g/cm3(Predicted)
[storage temp. ]

Keep Cold
[solubility ]

DMSO (Heated, Sonicated), Methanol (Slightly, Sonicated)
[form ]

Powder and Lumps
[pka]

8.44±0.10(Predicted)
[color ]

Light beige
[InChI]

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

KJJSHOHQQHACLE-UHFFFAOYSA-N
[SMILES]

C1=NC=C(O)C=C1C(OC)=O
Hazard InformationBack Directory
[Chemical Properties]

Light beige powder and lumps
[Uses]

Methyl 5-Hydroxynicotinate is an intermediate used to prepare selective cyclooxygenase-2 inhibitors. It is also used to prepare imino sugars as inhibitors of liver glycogen phosphorylase.
[Synthesis]

Methanol

67-56-1

5-Hydroxynicotinic acid

27828-71-3

Methyl 5-hydroxynicotinate

30766-22-4

Method A. Step A. Synthesis of methyl 5-hydroxynicotinate. 5-Hydroxynicotinic acid (833 g, 5.99 mol) was dissolved in methanol (6.7 L), and concentrated sulfuric acid (292 mL) was slowly added dropwise, with the rate of dropwise acceleration controlled to maintain the temperature of the reaction mixture at 30°C. After the dropwise addition, the reaction mixture was stirred under reflux conditions for 7 days. Upon completion of the reaction, the mixture was cooled to room temperature and concentrated under reduced pressure. Water (4 L) was added to the concentrate and the pH of the mixture was adjusted to 8 with sodium bicarbonate (NaHCO3), at which point a white solid precipitated. The mixture was stirred at room temperature for 1 h. The solid was collected by filtration and dried under vacuum at 60 °C for 3 days to afford the target product methyl 5-hydroxynicotinate (783 g, 85% yield) as a white solid. The product was characterized by 1H NMR (DMSO-d6, 400 MHz): δ 10.46 (s, 1H), 8.54 (s, 1H), 8.34-8.35 (d, J = 2.8 Hz, 1H), 7.59 (s, 1H), 3.85 (s, 3H).

[References]

[1] Patent: WO2015/164508, 2015, A1. Location in patent: Page/Page column 52
[2] Patent: WO2008/154563, 2008, A1. Location in patent: Page/Page column 91-92
[3] Bioorganic and Medicinal Chemistry Letters, 2018, vol. 28, # 4, p. 606 - 611
[4] Patent: WO2014/154727, 2014, A1. Location in patent: Page/Page column 43
[5] Patent: US2014/296239, 2014, A1. Location in patent: Paragraph 0114; 0115
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38-41-37/38
[Safety Statements ]

26-36/37/39-39-37/39
[WGK Germany ]

3
[Hazard Note ]

Irritant/Keep Cold
[HS Code ]

29333990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Sulfuric acid-->Thionyl chloride-->Sodium nitrite-->p-Toluenesulfonic acid-->5-Aminonicotinic acid-->Methanol-->5-Hydroxynicotinic acid
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 5-hydroxynicotinate(30766-22-4)MS
Methyl 5-hydroxynicotinate(30766-22-4)1HNMR
Methyl 5-hydroxynicotinate(30766-22-4)13CNMR
Methyl 5-hydroxynicotinate(30766-22-4)IR1
Methyl 5-hydroxynicotinate(30766-22-4)IR2
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