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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 80986Erstellt: 23. Oktober 2026

Diisopropylethylamine → Benzyl 4-({2-[(tert-butoxycarbonyl)amino]ethyl}[(4-chlorophenyl)methyl]carbamoyl)piperazine-1-carboxylate

https://huagongshe.com/de/reaction/80986

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt4-Cbz-piperazine-1-carbonyl ChlorideHCID 19358568—
EduktHCID 67134877HCID 67134877—
LösungsmittelDichloromethaneHCID 6344—
ProduktBenzyl 4-({2-[(tert-butoxycarbonyl)amino]ethyl}[(4-chlorophenyl)methyl]carbamoyl)piperazine-1-carboxylateHCID 5341658338%

Reaktionsschritte

Benzyl 4-(chlorocarbonyl)piperazine-1-carboxylate (233 mg, 0.83 mmol) was added at room temperature to a solution of tert-butyl 2-(4-chlorobenzylamino)ethylcarbamate (235 mg, 0.83 mmol) and Hunig's base (0.2 mL, 1.2 mmol, 1.5 eq.) in dichloromethane (1.6 mL). The reaction was allowed to stir overnight. The reaction mixture was then concentrated to the crude product, which was purified by flash column chromatography to afford benzyl 4-((2-(tert-butoxycarbonylamino)ethyl)(4-chlorobenzyl)carbamoyl)piperazine-1-carboxylate as foam (167 mg, 38%). MS (ESI) m/e (M+H+) 531.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846683B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-2c2b8616e830401d9e43f583e9e50b89
Quellennotizuspto-grants-2014_09