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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13699Erstellt: 23. Oktober 2026

Trifluoroacetic acid → N-[3-(1-ethyl-5-fluoro-indan-1-yl)-1H-indol-7-yl]-methanesulfonamide

https://huagongshe.com/de/reaction/13699

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
Eduktn-(1h-Indol-7-yl)methanesulfonamideHCID 20231824—
Edukt1-Ethyl-5-fluoroindan-1-olHCID 59340428—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-[3-(1-ethyl-5-fluoro-indan-1-yl)-1H-indol-7-yl]-methanesulfonamideHCID 1126877284,3%

Reaktionsschritte

Combine 1-ethyl-5-fluoro-indan-1-ol (502 mg, 2.79 mmol, 1.30 equivalents), N-(1H-Indol-7-yl)-methanesulfonamide (450 mg, 2.14 mmol, 1.00 equivalents), and trifluoroacetic acid (0.25 ml, 3.21 mmol, 1.50 equivalents) in dichloromethane (5 ml) and stir at room temperature under nitrogen overnight. Load the solution on silica and purify eluting with 0 to 100% ethyl acetate/hexanes over 25 minutes to obtain the title compound (672 mg, 84%). LC-MS m/z 373.0 (M++1). The racemic mixture is separated on a Chiralcel OJ 8×33 cm column eluting with methanol with 0.2% dimethylethylamine (flow: 375 ml/min, UV detection at 230 nm) to provide the individual enantiomers, Examples 1A and 1B, in 96.3% ee and 97.4% ee, respectively.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728150B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-fbe7d318a9d74414884f73b6d827b33f
Quellennotizuspto-grants-2010_06