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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561582Generated: October 26, 2026

Water → 3-{(4-Fluorophenyl)[4-(trifluoromethyl)phenyl]methyl}-7-[(methylsulfanyl)methyl]-1H-indole

https://huagongshe.com/reaction/561582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantindium(III)chlorideHCID 159675—
Reactantalpha-(4-Fluorophenyl)-4-(trifluoromethyl)benzenemethanolHCID 579773—
Reactant3-(2,4-Dichlorophenyl)-3-{5-fluoro-7-[(methylsulfanyl)methyl]-1H-indol-3-yl}propan-1-olHCID 58392305—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product3-{(4-Fluorophenyl)[4-(trifluoromethyl)phenyl]methyl}-7-[(methylsulfanyl)methyl]-1H-indoleHCID 58392363—

Reaction Conditions

Temperature80 °C

Reaction Steps

503 mg (1.86 mmol) of the compound from Example 80A and 75 mg (0.34 mmol) of indium(III) chloride were added to 300 mg (1.69 mmol) of the compound from Example 8 in 15 ml of toluene. The reaction mixture was stirred at 80° C. for 5 h, a further 187 mg (0.85 mmol) of indium(III) chloride were added, and the mixture was again stirred for 5 h. After cooling to RT, the reaction solution was mixed with water and ethyl acetate, and the solid was filtered off. The phases of the filtrate were separated, and the aqueous phase was extracted with ethyl acetate. The combined organic phases were dried over sodium sulfate, filtered and concentrated. Purification of the crude product by preparative HPLC (mobile phase: acetonitrile/water gradient) resulted in 107 mg (15% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063234B2
Source datasetuspto-grants-2011_11
ORD IDord-728b952883bb4306aead89e8d51c5b61
Source noteuspto-grants-2011_11