Reaktion #85819

Reaktionsgleichung

(R)-tert-butyl 3-aminopyrrolidine-1-carboxylate

TMS-NCO

DIPEA

→

crude title compound

(R)-tert-butyl 3-ureidopyrrolidine-1-carboxylate

Lösungsmittel

dichloromethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   Einengenwas concentrated in vacuo
2. 2
   workup.ADDITIONThe residue was treated with EtOAc/H2O
3. 3
   Waschenwashed with brine
4. 4
   Trocknendried over anhydrous sodium sulfate
5. 5
   Filtrationfiltered
6. 6
   Einengenconcentrated

Vorschrift

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.

Quelle