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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838363Generated: October 26, 2026

Dichloromethane → 2-Cyano-1-(4-fluorobenzyl)-5-methanesulfonylindole

https://huagongshe.com/reaction/1838363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylamineHCID 8471—
Reactant1-(4-Fluorobenzyl)-5-methanesulfonylindole-2-carboxamideHCID 22504369—
SolventWaterHCID 962—
Product2-Cyano-1-(4-fluorobenzyl)-5-methanesulfonylindoleHCID 2250444871.7%

Reaction Steps

To a mixture of 1-(4-fluorobenzyl)-5-methanesulfonylindole-2-carboxamide (100 mg) and dichloromethane (2 ml), triethylamine (0.09 ml) and anhydrous trifluoroacetic acid (0.09 ml) were added at 15 to 30° C. and the mixture was stirred at the same temperature for 2 hours. Water was added therto, and the mixture was extracted with dichloromethane. The organic layer was washed with water, dried over sodium sulfate and concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography (hexane:ethyl acetate=2:1) to obtain 68 mg of the desired product as a white crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06673797B1
Source datasetuspto-grants-2004_01
ORD IDord-ecba265a845742cb992afb7ab63a0172
Source noteuspto-grants-2004_01