ChemicalBook--->CAS DataBase List--->167631-21-2

167631-21-2

167631-21-2 Structure

167631-21-2 Structure
IdentificationBack Directory
[Name]

ethyl 5-fluoro-3-iodo-1H-indole-2-carboxylate
[CAS]

167631-21-2
[Synonyms]

5-fluoro-3-iodo-1H-indole
ethyl 5-fluoro-3-iodo-1H-indole-2-carboxylate
5-Fluoro-3-iodo-1H-indole-2-carboxylic acid ethyl ester
1H-Indole-2-carboxylic acid, 5-fluoro-3-iodo-, ethyl ester
[Molecular Formula]

C11H9FINO2
[MDL Number]

MFCD13184347
[MOL File]

167631-21-2.mol
[Molecular Weight]

333.1
Chemical PropertiesBack Directory
[density ]

1.824
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Hazard InformationBack Directory
[Synthesis]

ETHYL 5-FLUOROINDOLE-2-CARBOXYLATE

348-36-7

ethyl 5-fluoro-3-iodo-1H-indole-2-carboxylate

167631-21-2

Method A: Ethyl 5-fluoroindole-2-carboxylate (1.0 eq.) was mixed with a DMF solution (5 mL) of KOH (4.0 eq.) at room temperature and stirred until a homogeneous suspension was formed. Subsequently, DMF solution (3 mL) of iodine (1.0 eq.) was added slowly and dropwise. The reaction mixture was stirred at room temperature for 1.5 hours. Upon completion of the reaction, the mixture was poured into a mixture consisting of saturated aqueous NaHSO3 solution (15 mL), 30% NH4OH (2 mL) and water (15 mL). The resulting solid product was collected by filtration and dried under reduced pressure, and the resulting ethyl 5-fluoro-3-iodo-1H-indole-2-carboxylate was used for subsequent reactions without further purification.

[References]

[1] European Journal of Medicinal Chemistry, 2012, vol. 49, p. 379 - 396
[2] European Journal of Organic Chemistry, 2018, vol. 2018, # 45, p. 6314 - 6327
[3] Journal of Medicinal Chemistry, 2008, vol. 51, # 12, p. 3414 - 3421
[4] European Journal of Organic Chemistry, 2008, # 30, p. 5162 - 5175
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