Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 216019Erstellt: 25. Oktober 2026

Dicyclohexylcarbodiimide → Tert-butyl 4-(3-(4-fluorophenoxy)phenylcarbamoyl)-4-methylpiperidine-1-carboxylate

https://huagongshe.com/reaction/216019

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDicyclohexylcarbodiimideHCID 10868—
EduktHOAtHCID 181649—
Edukt1-[(Tert-butoxy)carbonyl]-4-methylpiperidine-4-carboxylic acidHCID 23282848—
Edukt3-(4-Fluorophenoxy)anilineHCID 23506015—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
ProduktTert-butyl 4-(3-(4-fluorophenoxy)phenylcarbamoyl)-4-methylpiperidine-1-carboxylateHCID 68989388—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

1-(tert-butoxycarbonyl)-4-methylpiperidine-4-carboxylic acid (243 mg, 1.0 mmol), 3-(4-fluorophenoxy)aniline (203 mg, 1.0 mmol), DCC (206 mg, 1.0 mmol), and HOAt (138 mg, 1.01 mmol) were combined in EtOAc (50 mL) and DMF (5 mL). The reaction mixture was heated at 80° C. for 20 hours. Most of the EtOAc was evaporated, resulting in precipitation of a solid, which was removed by filtration. The filtrate was diluted with EtOAc, washed with 1 N aq. HCl, water, and brine, dried, and concentrated under vacuum to give the title compound. MS (ES+) [M+H]+=429.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08193202B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-6984cfa846b849f798264fda96d7ebfc
Quellennotizuspto-grants-2012_06