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2-(4-Fluorophenyl)-5-[(5-iodo-2-methylphenyl)methyl]thiophene

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2-(4-Fluorophenyl)-5-[(5-iodo-2-methylphenyl)methyl]thiophene Basic information

Product Name:
2-(4-Fluorophenyl)-5-[(5-iodo-2-methylphenyl)methyl]thiophene
Synonyms:
  • Thiophene, 2-(4-fluorophenyl)-5-[(5-iodo-2-methylphenyl)methyl]-
  • 2-(4-Fluorophenyl)-5-[(5-iodo-2-methylphenyl)methyl]thiophene
  • 2-(4-Fluorophenyl)-5-(5-iodo-2-Methylbenzyl)thiophene
  • Canagliflozin iMpurity D
  • 2-((5-IODO-2-METHYLPHENYL)METHYL)-5-(4-FLUOROPHENYL)THIOPHENE
  • Canagliflozin INT5
  • Canagliflozin Intermediate1
  • 2-(4-Fluorophenyl)
CAS:
898566-17-1
MF:
C18H14FIS
MW:
408.27
EINECS:
618-312-6
Product Categories:
  • 898566-17-1
Mol File:
898566-17-1.mol
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2-(4-Fluorophenyl)-5-[(5-iodo-2-methylphenyl)methyl]thiophene Chemical Properties

Melting point:
109-110 °C
Boiling point:
450.2±45.0 °C(Predicted)
Density 
1.533
vapor pressure 
0-0Pa at 20-25℃
storage temp. 
2-8°C(protect from light)
solubility 
DMSO (Sparingly), Methanol (Slightly)
form 
Solid
color 
Pale Yellow
InChI
InChI=1S/C18H14FIS/c1-12-2-7-16(20)10-14(12)11-17-8-9-18(21-17)13-3-5-15(19)6-4-13/h2-10H,11H2,1H3
InChIKey
MGXZKAYHSITHMW-UHFFFAOYSA-N
SMILES
C1(C2=CC=C(F)C=C2)SC(CC2=CC(I)=CC=C2C)=CC=1
LogP
7.5 at pH7
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2-(4-Fluorophenyl)-5-[(5-iodo-2-methylphenyl)methyl]thiophene Usage And Synthesis

Chemical Properties

Pale Yellow Solid.

Uses

2-(4-Fluorophenyl)-5-[(5-iodo-2-methylphenyl)methyl]thiophene is an antidiabetic agent and a Canagliflozin (C175190) intermediate. Canagliflozin is a sodium/glucose cotransporter 2 (SGLT2) inhibitor and a candidate for the treatment of type 2 diabetes and obesity.

Synthesis

1030825-20-7

898566-17-1

2-(5-bromo-2-methylbenzyl)-5-(4-fluorophenyl)thiophene (100 g; cf. WO 2005/012326) was dissolved in toluene (300 mL) at room temperature and under nitrogen atmosphere. To this solution, sodium iodide (83 g), cuprous(I) iodide (2.64 g), N,N'-dimethylethylenediamine (2.94 mL) and diethylene glycol dimethyl ether (50 mL) were added sequentially. The reaction mixture was heated to reflux temperature and stirred continuously for 36 hours. Upon completion of the reaction, ethyl acetate (300 mL) was added to the mixture at 40 °C and filtered through a filter pre-coated with activated carbon. The filtrate was washed and concentrated. The resulting residue was suspended in methanol (426 mL) at reflux temperature for 75 minutes. Subsequently, the suspension was cooled to 25 °C and stirring was continued for 1 hour. The precipitate was collected by filtration, washed with methanol and dried under vacuum at 50 °C to afford 2-(5-iodo-2-methylbenzyl)-5-(4-fluorophenyl)thiophene (94.9 g) in white crystalline form. The mass spectrum (APCI) showed a m/z of 409 (M + H); the melting point was 109-110°C. The crystal was found to have the following properties.

References

[1] Patent: WO2009/35969, 2009, A1. Location in patent: Page/Page column 77
[2] Patent: US2010/99883, 2010, A1. Location in patent: Page/Page column 43
[3] Patent: US2016/228375, 2016, A1. Location in patent: Paragraph 0097; 0098

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