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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 62699Erstellt: 25. Oktober 2026

Pyrrolidine → N-(2-amino-5-bromophenyl)pyrrolidine-1-carboxamide

https://huagongshe.com/reaction/62699

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyrrolidineHCID 31268—
EduktTriphosgeneHCID 94429—
Edukt5-Bromo-2-nitroanilineHCID 5314766—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(2-amino-5-bromophenyl)pyrrolidine-1-carboxamideHCID 8671253734,4%

Reaktionsschritte

To a solution of 5-bromo-2-nitroaniline (1 g, 4.61 mmol) in dichloromethane (15 mL) were added TEA (8.35 mL, 59.9 mmol, 1.3 eq.) and triphosgene (1.37 g, 4.61 mmol, 1 equiv.) at 0° C. The mixture was stirred for three hours at room temperature and the pyrrolidine (0.39 g, 5.53 mmol, 1.2 equiv.) was added slowly. The reaction was stirred for an additional two hours. The reaction crude was diluted with dichloromethane and washed with water and brine. The organic layers were dried over MgSO4, filtered and evaporated. The residue was purified by column chromatography on eluting ethyl acetate and hexane to allow N-(2-amino-5-bromophenyl)pyrrolidine-1-carboxamide (0.45 g, 31% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09447030B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-bc741af4a26c43ffb06e37aa6e257499
Quellennotizuspto-grants-2016_09