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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561680Generated: October 26, 2026

Trifluoroacetic acid → 3-[(4-Chlorophenyl)(2,2-difluorocyclopropyl)methyl]-7-[(methylsulfonyl)methyl]-1H-indole

https://huagongshe.com/reaction/561680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactantindium(III)chlorideHCID 159675—
Reactant7-[(Methylsulfonyl)methyl]-1H-indoleHCID 58392294—
Reactant(4-Chlorophenyl)(2,2-difluorocyclopropyl)methanolHCID 58392413—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
Product3-[(4-Chlorophenyl)(2,2-difluorocyclopropyl)methyl]-7-[(methylsulfonyl)methyl]-1H-indoleHCID 58392192—

Reaction Steps

In three parallel batches in each case 3.08 g (13.9 mmol) of indium(III) chloride and 1.6 ml (20.9 mmol) of trifluoroacetic acid were added to in each case 2.54 g (11.6 mmol) of the compound from Example 159A and 2.92 g (13.9 mmol) of the compound from Example 86A in 125 ml of 1,2-dichloroethane, and the mixture was heated under reflux overnight. It was diluted in each case with dichloromethane, and the three batches were combined and washed with saturated aqueous sodium bicarbonate solution, water and saturated aqueous sodium chloride solution, dried over magnesium sulfate, filtered through kieselguhr and concentrated. The residue was purified by preparative SFC (ethylpyridine column; mobile phase: carbon dioxide/methanol gradient; 150 bar; 35° C.) to result in 995 mg (7% of theory) of the title compound as mixture of diastereomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063234B2
Source datasetuspto-grants-2011_11
ORD IDord-e2512a05c353428685d6fef2d48f6ad7
Source noteuspto-grants-2011_11