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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561584Generated: October 25, 2026

Water → 3-[(4-Fluoro-2-methylphenyl)(4-fluorophenyl)methyl]-7-[(methylsulfanyl)methyl]-1H-indole

https://huagongshe.com/reaction/561584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantindium(III)chlorideHCID 159675—
Reactant(4-Fluoro-2-methylphenyl)(4-fluorophenyl)methanolHCID 58392149—
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-Fluoro-2-methylphenyl)(4-fluorophenyl)methyl]-7-[(methylsulfanyl)methyl]-1H-indoleHCID 44595236—

Reaction Conditions

Temperature80 °C

Reaction Steps

509 mg (2.17 mmol) of the compound from Example 82A and 437 mg (1.97 mmol) of indium(III) chloride were added to 350 mg (1.97 mmol) of the compound from Example 8 in 15 ml of toluene. The reaction mixture was stirred at 80° C. 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 174 mg (22% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063234B2
Source datasetuspto-grants-2011_11
ORD IDord-582347a2ca0841c687b16d7d189cb27a
Source noteuspto-grants-2011_11