4-CHLORO-6-IODOQUINOLINE Chemical Properties

Melting point:

138-140℃

Boiling point:

338℃

Density 

1.919

Flash point:

158℃

storage temp. 

under inert gas (nitrogen or Argon) at 2–8 °C

pka

2.81±0.16(Predicted)

Appearance

Off-white to light yellow Solid

InChI

InChI=1S/C9H5ClIN/c10-8-3-4-12-9-2-1-6(11)5-7(8)9/h1-5H

InChIKey

XPXHGYKMODLJBY-UHFFFAOYSA-N

SMILES

N1C2C(=CC(I)=CC=2)C(Cl)=CC=1

4-CHLORO-6-IODOQUINOLINE Usage And Synthesis

Uses

4-Chloro-6-iodoquinoline is a commonly used synthetic intermediate in the fields of medicine and materials science, and can be used for cross-coupling reactions to synthesize different diarylquinoline compounds.

Synthesis

The general procedure for the synthesis of 4-chloro-6-iodoquinoline from 6-iodo-4-hydroxyquinoline was as follows: 6-iodo-4-hydroxyquinoline (100 g, 369 mmol) was suspended in phosphorus oxychloride (POCl3, 340 mL, 3.7 mol) at room temperature. After 1 hour of reaction, the reaction mixture was concentrated. The concentrated residue was carefully placed in an ice water bath and neutralized with saturated sodium bicarbonate solution. The resulting brown suspension was filtered and the solid was washed with water (2 x 500 mL) and subsequently dried under vacuum overnight to afford 4-chloro-6-iodoquinoline as a brown solid (103 g, 92% yield). The product was characterized by 1H NMR (400 MHz, DMSO-d6): δ 8.88 (d, J = 4.8 Hz, 1H), 8.54 (d, J = 1.8 Hz, 1H), 8.15 (dd, J = 8.8, 2.0 Hz, 1H), 7.88 (d, J = 8.8 Hz, 1H), 7.82 (d, J = 4.8 Hz, 1H); mass spectrum (MS) showed m/z of 289.9 ([M + H]+).

References

[1] Patent: US2012/41024, 2012, A1. Location in patent: Page/Page column 8; 10; 16
[2] Patent: EP2566477, 2015, B1. Location in patent: Paragraph 0157; 0160
[3] Journal of Medicinal Chemistry, 2016, vol. 59, # 10, p. 4867 - 4880
[4] Patent: WO2005/63739, 2005, A1. Location in patent: Page/Page column 64

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