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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 62691Erstellt: 24. Oktober 2026

Triphosgene → Tert-butyl 4-((3-(2-nitro-5-(thiophen-2-yl)phenyl)ureido)methyl)piperidine-1-carboxylate

https://huagongshe.com/de/reaction/62691

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphosgeneHCID 94429—
Edukt1-Boc-4-(aminomethyl)piperidineHCID 736817—
Edukt2-Nitro-5-(thiophen-2-yl)anilineHCID 23656428—
LösungsmittelDichloromethaneHCID 6344—
ProduktTert-butyl 4-((3-(2-nitro-5-(thiophen-2-yl)phenyl)ureido)methyl)piperidine-1-carboxylateHCID 7100732025%

Reaktionsschritte

To a solution of 2-nitro-5-(thiophen-2-yl)aniline (0.60 g, 2.72 mmol, 1.0 equiv.) in dichloromethane at 0° C. were added TEA (5 mL, 35.4 mmol, 13 equiv.) and triphosgene (0.81 g, 2.72 mmol, 1.0 equiv.). The mixture was warmed to room temperature and stirred 3 h. The reaction was then cooled to 0° C. and tert-butyl 4-(aminomethyl)piperidine-1-carboxylate (0.88 g, 4.09 mmol, 1.5 equiv.) was then added slowly. The reaction mixture was slowly warmed to room temperature and stirred for 2 h. The reaction was diluted with dichloromethane, washed with water and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated. The crude residue was purified by column chromatography (silica gel, EtOAc/hexanes) to afford tert-butyl 4-((3-(2-nitro-5-(thiophen-2-yl)phenyl)ureido)methyl)piperidine-1-carboxylate (0.31 g, 25% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09447030B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-265b362c21ef42d69879b38d34beb98d
Quellennotizuspto-grants-2016_09