Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 57541Erstellt: 25. Oktober 2026

Trimethylsilyl isocyanate → (R)-tert-butyl 3-ureidopyrrolidine-1-carboxylate

https://huagongshe.com/reaction/57541

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethylsilyl isocyanateHCID 70696—
EduktDiisopropylethylamineHCID 81531—
Edukt(R)-(+)-1-Boc-3-aminopyrrolidineHCID 854070—
LösungsmittelDichloromethaneHCID 6344—
Produkt(R)-tert-butyl 3-ureidopyrrolidine-1-carboxylateHCID 71113416—

Reaktionsschritte

To a solution of (R)-tert-butyl 3-aminopyrrolidine-1-carboxylate (180 mg, 1 mmol) in dichloromethane was added TMS-NCO (1 g, 8.7 mmol) and DIPEA (1.2 g, 10 mmol). The mixture was stirred at room temperature overnight, then was concentrated in vacuo. The residue was treated with EtOAc/H2O, the organic layer was combined, washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated to give the crude title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434726B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-03b908eb6c974305becfdd62d3cb84c4
Quellennotizuspto-grants-2016_09