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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 68759Erstellt: 25. Oktober 2026

4-Iodobenzoic acid → 4-[Cyclopropyl-(4-iodo-benzoyl)-amino]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/68759

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Iodobenzoic acidHCID 12085—
EduktDiisopropylethylamineHCID 81531—
EduktO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Edukttert-Butyl 4-(cyclopropylamino)piperidine-1-carboxylateHCID 2769591—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-[Cyclopropyl-(4-iodo-benzoyl)-amino]-piperidine-1-carboxylic acid tert-butyl esterHCID 68290220—

Reaktionsschritte

2-(1H-Benzotriazol-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (2.67 g) is added to a solution of 4-iodo-benzoic acid (2.06 g) and ethyldiisopropylamine (2.88 mL) in N,N-dimethylformamide (15 mL) at room temperature. The solution is stirred for 10 min prior to the addition of 4-cyclopropylamino-piperidine-1-carboxylic acid tert-butyl ester (2.00 g). The resulting mixture stirred at room temperature overnight. The mixture is concentrated in vacuo and the residue is mixed with water and ethyl acetate. The organic phase is separated, washed with water and aqueous NaHCO3 solution, dried, and the solvent is evaporated. The crude product is used for the next reaction step without further purification. LC (method 5): tR=2.32 min; Mass spectrum (ESI+): m/z=471 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822471B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-464cde27ee4d4693b998c15da72b5346
Quellennotizuspto-grants-2014_09