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40055-37-6

40055-37-6 Structure

40055-37-6 Structure
IdentificationBack Directory
[Name]

Pyridine, 3-(4,5-dihydro-2-oxazolyl)-
[CAS]

40055-37-6
[Synonyms]

Nicorandil Impurity 3
Nicorandil EP Impurity D
2-(3-Pyridyl)-2-oxazoline
2-(Pyridin-3-yl)-4,5-dihydrooxazole
Pyridine, 3-(4,5-dihydro-2-oxazolyl)-
2-pyridin-3-yl-4,5-dihydro-1,3-oxazole
Nicorandil Impurity 4(Nicorandil EP Impurity D)
[Molecular Formula]

C8H8N2O
[MDL Number]

MFCD00183228
[MOL File]

40055-37-6.mol
[Molecular Weight]

148.16
Chemical PropertiesBack Directory
[Melting point ]

71 °C
[Boiling point ]

260 °C
[density ]

1.23±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[solubility ]

Chloroform (Slightly), Ethyl Acetate (Slightly)
[form ]

Solid
[pka]

4.13±0.12(Predicted)
[color ]

Off-White to Pale Yellow
[Stability:]

Hygroscopic
[Major Application]

pharmaceutical
pharmaceutical small molecule
[InChI]

InChI=1S/C8H8N2O/c1-2-7(6-9-3-1)8-10-4-5-11-8/h1-3,6H,4-5H2
[InChIKey]

FVASBRDDSBRETH-UHFFFAOYSA-N
[SMILES]

C1=NC=CC=C1C1=NCCO1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

2-(3-Pyridyl)-2-oxazoline is an impurity of Nicorandil (N398500). Nicorandil impurity E.
[Synthesis]

3-Pyridinecarboxaldehyde

500-22-1

Monoethanolamine

141-43-5

Pyridine, 3-(4,5-dihydro-2-oxazolyl)-

40055-37-6

General procedure for the synthesis of 3-(4,5-dihydro-2-oxazolyl)-pyridine from 3-pyridinecarboxaldehyde and 2-aminoethanol: To a solution of 3-pyridinecarboxaldehyde (79 mg, 0.5 mmol), 2-aminoethanol (200 μL, 3.2 mmol), and pyridine (80 μL, 1.0 mmol) in methanol (6 mL) was added PTAB (trimethylphenyltrimethyl ammonium trimethylammonium tribromide, 376 mg, 1.0 mmol). The reaction mixture was stirred at room temperature for 22 hours and then treated with 0.5 M aqueous Na2S2O3 (10 mL) and 1.0 M aqueous NaHCO3 (15 mL), followed by extraction with EtOAc (60 mL). The organic layer was washed sequentially with 0.5 M Na2S2O3 aqueous solution and saturated NaCl aqueous solution and dried with MgSO4. After the solvent was removed under vacuum, the residue was purified by column chromatography on silica gel (Wako C-200), the eluent being a mixture of CCl4 and CCl4-CHCl3 (2:1 v/v) to afford 3-(4,5-dihydro-2-oxazolyl)-pyridine (85 mg) in 86% yield.

[References]

[1] Heterocycles, 2017, vol. 94, # 5, p. 979 - 990
Spectrum DetailBack Directory
[Spectrum Detail]

Pyridine, 3-(4,5-dihydro-2-oxazolyl)-(40055-37-6)1HNMR
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