Basic information Safety Supplier Related

5-Fluoroisatonic anhydride

Basic information Safety Supplier Related

5-Fluoroisatonic anhydride Basic information

Product Name:
5-Fluoroisatonic anhydride
Synonyms:
  • 6-FLUORO-2H-3,1-BENZOXAZINE-2,4(1H)-DIONE
  • 6-fluoro-1H-benzo[d][1,3]oxazine-2,4-dione
  • 6-fluoro-1H-3,1-benzoxazine-2,4-dione
  • 6-fluoro-1H-3,1-benzoxazine-2,4-quinone
  • 6-FLUORO ISATIN ANHYDRIDE
  • 5-FLUOROISATOIC ANHYDRIDE
  • 5-FLUOROISATONIC ANHYDRIDE
  • 6-Fluorobenzo[d][1,3]oxazine-2,4-dione
CAS:
321-69-7
MF:
C8H4FNO3
MW:
181.12
EINECS:
640-488-8
Product Categories:
  • Miscellaneous
  • Aromatics
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
Mol File:
321-69-7.mol
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5-Fluoroisatonic anhydride Chemical Properties

Melting point:
259-262°C
Density 
1.502±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
soluble in DMSO
pka
9.61±0.20(Predicted)
form 
powder
color 
Off-white to pale yellow
InChI
InChI=1S/C8H4FNO3/c9-4-1-2-6-5(3-4)7(11)13-8(12)10-6/h1-3H,(H,10,12)
InChIKey
UBKGOWGNYKVYEF-UHFFFAOYSA-N
SMILES
N1C2=CC=C(F)C=C2C(=O)OC1=O
CAS DataBase Reference
321-69-7(CAS DataBase Reference)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36
HazardClass 
IRRITANT
HS Code 
2934999090
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5-Fluoroisatonic anhydride Usage And Synthesis

Chemical Properties

Dark yellow Solid

Uses

5-Fluoroisatoic Anhydride is a versatile pharmaceutical intermediate used in the preparation of insulin secretagogues, HCV polymerase inhibitors, anxiolytic agents and other bioactive compounds.

Preparation

5-Fluoroisatonic anhydride is prepared from 5-fluoro indole (9d) by stirring in a 4:1 mixture of DMF/H2O for 16 h at room temperature.
1 H NMR (DMSO-d6): δ11.19 (s, br., 1H), 7.36 (dd, J = 8.4, 2.6 Hz, 1H), 6.87 (dt, J = 8.4, 2.2 Hz, 1H), 6.74 (dd, J = 9.3, 2.2 Hz, 1H).

Synthesis

443-69-6

321-69-7

Preparation of compound 1: Synthesis of 5-fluoroisocyanic anhydride. In a 250 mL three-necked flask assembled with a magnetic stir bar and condenser, acetic anhydride (90.0 mL), 5-fluoroindigo (20.62 g, 0.125 mol, 1.00 equiv.) and acetic acid (90 mL) were added sequentially. The reaction system was placed in a water bath and heated to 85 °C. Subsequently, chromium(VI) oxide (20.36 g, 0.204 mol, 1.63 eq.) was added in batches (~0.5 g per batch) to the red solution over 40 minutes. After addition, the reaction mixture was continued to be stirred for 15 minutes and subsequently cooled to 10 °C in an ice bath. The resulting solid product was separated by filtration and washed with 400 mL of water to remove most of the green impurities. The resulting solid was dissolved in 300 mL of a 2:1 (v/v) acetic acid/water mixture, filtered again, and dried overnight in a vacuum oven at 50 °C to afford 5-fluoroisocyanic anhydride as a bright yellow solid (14.45 g, 64% yield).

References

[1] Catalysis Science and Technology, 2015, vol. 5, # 10, p. 4830 - 4838
[2] Angewandte Chemie, 1980, vol. 92, # 3, p. 196 - 197
[3] Patent: US5863944, 1999, A
[4] Journal of the Chemical Society, 1957, p. 2916,2917
[5] Journal of medicinal chemistry, 1971, vol. 14, # 12, p. 1233 - 1235

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