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ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyridine compound >  Dihydropyridine >  4,5-DIHYDRO-4-OXOFURO[3,2-C]PYRIDINE

4,5-DIHYDRO-4-OXOFURO[3,2-C]PYRIDINE

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4,5-DIHYDRO-4-OXOFURO[3,2-C]PYRIDINE Basic information

Product Name:
4,5-DIHYDRO-4-OXOFURO[3,2-C]PYRIDINE
Synonyms:
  • FURO[3,2-C]PYRIDIN-4(5H)-ONE
  • 4-OXO-4,5-DIHYDROFURO[3,2-C]PYRIDINE
  • 4,5-DIHYDRO-4-OXOFURO[3,2-C]PYRIDINE
  • 4,5-Dihyro-4-Oxofuro[3,2]Pyridine
  • 4H,5H-furo[3,2-c]pyridin-4-one
  • 5H-Furo[3,2-c]pyridin-4-one
  • Furo[3,2-c]pyridin-4-ol
  • 108561
CAS:
26956-43-4
MF:
C7H5NO2
MW:
135.12
EINECS:
125-856-9
Product Categories:
  • Fused Ring Systems
Mol File:
26956-43-4.mol
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4,5-DIHYDRO-4-OXOFURO[3,2-C]PYRIDINE Chemical Properties

Melting point:
202-204 °C
Boiling point:
372.8±42.0 °C(Predicted)
Density 
1.288±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
12.11±0.20(Predicted)
Appearance
Light yellow to yellow Solid
InChI
InChI=1S/C7H5NO2/c9-7-5-2-4-10-6(5)1-3-8-7/h1-4H,(H,8,9)
InChIKey
FYNCIYHECMWXPK-UHFFFAOYSA-N
SMILES
C1(=O)NC=CC2OC=CC1=2
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Safety Information

Hazard Codes 
T
Risk Statements 
25
Safety Statements 
45
RIDADR 
2811
HazardClass 
6.1
PackingGroup 
HS Code 
2934999090
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4,5-DIHYDRO-4-OXOFURO[3,2-C]PYRIDINE Usage And Synthesis

Synthesis

119924-26-4

26956-43-4

The general procedure for the synthesis of 4,5-dihydro-4-oxofuro[3,2]pyridine from (E)-3-(furan-2-yl)acryloyl azide was as follows: (E)-3-(furan-2-yl)acryloyl azide (150 g, 920 mmol) was added to toluene (800 mL) preheated to 100 °C and the reaction mixture was stirred for 30 min. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was dissolved in o-dichlorobenzene (800 mL) and iodine (1 g) was added as a catalyst. The reaction mixture was stirred at 180 °C for 2 h, followed by evaporation under reduced pressure to remove the solvent. The residue was dissolved in methanol, the precipitate was collected by filtration and the filtrate was concentrated under reduced pressure. Finally, the residue was washed with diisopropyl ether to afford the target product 4,5-dihydro-4-oxofuro[3,2]pyridine (100 g, 80% yield). The product was characterized by 1H-NMR (DMSO-d6): δ 6.85 (1H, dd, J = 7.1, 1.0 Hz), 6.92 (1H, dd, J = 1.9, 1.0 Hz), 7.29 (1H, d, J = 7.1 Hz), 7.86 (1H, d, J = 1.9 Hz), 11.42 (1H, brs).

References

[1] Patent: EP2100895, 2009, A1. Location in patent: Page/Page column 44
[2] Patent: WO2013/163244, 2013, A1. Location in patent: Paragraph 00273
[3] Patent: WO2016/37578, 2016, A1. Location in patent: Page/Page column 146
[4] Patent: WO2004/100947, 2004, A2. Location in patent: Page 20-21; 16
[5] Patent: WO2005/67900, 2005, A2. Location in patent: Page/Page column 39-40

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