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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1838363Erstellt: 27. Oktober 2026

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

https://huagongshe.com/reaction/1838363

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktTrifluoroacetic acidHCID 6422—
EduktTriethylamineHCID 8471—
Edukt1-(4-Fluorobenzyl)-5-methanesulfonylindole-2-carboxamideHCID 22504369—
LösungsmittelWaterHCID 962—
Produkt2-Cyano-1-(4-fluorobenzyl)-5-methanesulfonylindoleHCID 2250444871,7%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06673797B1
Quelldatensatzuspto-grants-2004_01
ORD IDord-ecba265a845742cb992afb7ab63a0172
Quellennotizuspto-grants-2004_01