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455-70-9

455-70-9 Structure

455-70-9 Structure
IdentificationBack Directory
[Name]

METHYL 5-FLUOROPYRIDINE-3-CARBOXYLATE
[CAS]

455-70-9
[Synonyms]

Methyl5-fluoronicotinate
5-Fluoro-nicotinic acid methyl ester
Methyl 5-fluoro-3-pyridinecarboxylate
METHYL 5-FLUOROPYRIDINE-3-CARBOXYLATE
5-fluoro-2-methyl-3-pyridinecarboxylate
5-fluoro-3-pyridinecarboxylic acid methyl ester
5-Fluoropyridine-3-carboxylic acid methyl ester
3-Pyridinecarboxylic acid, 5-fluoro-, methyl ester
3-PYRIDINECARBONYL CHLORIDE, 5-FLUORO-, METHYL ESTER
METHYL 5-FLUOROPYRIDINE-3-CARBOXYLATE ISO 9001:2015 REACH
[Molecular Formula]

C7H6FNO2
[MDL Number]

MFCD01692049
[MOL File]

455-70-9.mol
[Molecular Weight]

155.13
Chemical PropertiesBack Directory
[Melting point ]

48 °C
[Boiling point ]

194.5±25.0 °C(Predicted)
[density ]

1.243±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[form ]

solid
[pka]

0.77±0.20(Predicted)
[Appearance]

White to off-white Solid
[InChI]

1S/C7H6FNO2/c1-11-7(10)5-2-6(8)4-9-3-5/h2-4H,1H3
[InChIKey]

PGCFLXMMCWKPDU-UHFFFAOYSA-N
[SMILES]

O=C(OC)C1=CN=CC(F)=C1
Safety DataBack Directory
[Risk Statements ]

36/37/38
[Safety Statements ]

26-37/39
[WGK Germany ]

WGK 3
[HazardClass ]

IRRITANT
[HS Code ]

29333990
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Methyl 5-aminopyridine-3-carboxylate
Hazard InformationBack Directory
[Chemical Properties]

Light yellow solid
[Uses]

Methyl 5-fluoronicotinate
[Synthesis]

Methyl 5-aminopyridine-3-carboxylate

36052-25-2

METHYL 5-FLUOROPYRIDINE-3-CARBOXYLATE

455-70-9

Example 2.26: Synthesis of methyl 5-fluoronicotinate; To a stirring solution of 243 mg (1.6 mmol) of methyl 5-aminonicotinate dissolved in 5 mL of HF-pyridine at 0 °C was slowly added 119 mg (1.72 mmol) of sodium nitrite (NaNO2). The reaction mixture was stirred continuously at 0 °C for 30 min, then warmed up to 50 °C and kept for 1 hour. Upon completion of the reaction, the reaction was quenched with ice and saturated sodium bicarbonate (NaHCO3) solution. The aqueous phase was extracted with chloroform (CHCl3) and the organic phase was dried over anhydrous sodium sulfate (Na2SO4), filtered and concentrated. Purification by fast silica gel column chromatography (eluent: 1% methanol/chloroform) afforded 139 mg of methyl 5-fluoronicotinate as a yellow solid in 56% yield.

[References]

[1] Patent: WO2006/110668, 2006, A1. Location in patent: Page/Page column 62
[2] Journal of Organic Chemistry, 1949, vol. 14, p. 328,331
[3] Angewandte Chemie - International Edition, 2018, vol. 57, # 31, p. 9896 - 9900
[4] Angew. Chem., 2018, vol. 130, p. 10044 - 10048,5
Spectrum DetailBack Directory
[Spectrum Detail]

METHYL 5-FLUOROPYRIDINE-3-CARBOXYLATE(455-70-9)1HNMR
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