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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 988622Erstellt: 26. Oktober 2026

2-Bromo-4-chloroaniline → 2-[(4-Boc-piperazin-1-ylcarbonyl)amino]-5-chlorobromobenzene

https://huagongshe.com/reaction/988622

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Bromo-4-chloroanilineHCID 70110—
EduktDiisopropylethylamineHCID 81531—
EduktTriphosgeneHCID 94429—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-[(4-Boc-piperazin-1-ylcarbonyl)amino]-5-chlorobromobenzeneHCID 21906538191,1%

Reaktionsschritte

To a stirring solution of triphosgene (2.7 g, 9.0 mmol) in dichloromethane (100 mL) was added, dropwise via an addition funnel, a solution of 2-bromo-4-chloroaniline (5 g, 24.2 mmol) and N,N-diisopropylethylamine (6.9 g, 53.2 mmol) in dichloromethane (50 mL). After complete addition and an additional hour, a solution of N-Boc-piperazine (5 g, 26.6 mmol) in dichloromethane (50 mL) was added. After stirring overnight, the solvent was removed in vacuo and the residue was partitioned between ethyl acetate and water. The organic phase was separated and washed consecutively with 1 M citric acid, brine, sat. aq sodium bicarbonate and finally with brine, then dried with MgSO4, filtered and concentrated in vacuo. The residue was then dissolved in a minimal amount of chloroform and chromatographed over silica gel, eluting with 20% ethyl acetate in hexanes followed by 30% ethyl acetate in hexanes. The product containing fractions were combined and concentrated in vacuo and the resulting solid was suspended in diethyl ether, sonicated and then filtered and dried in vacuo to give 7.2 g (71%) of a white powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06635657B1
Quelldatensatzuspto-grants-2003_10
ORD IDord-d7e4e3d9262843f78eda677a727a6669
Quellennotizuspto-grants-2003_10