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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 384698Erstellt: 25. Oktober 2026

Triethylamine → Benzyl 4-((5-bromo-2-pivalamidopyridin-4-ylamino)methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/384698

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt4-Aminomethyl-1-N-Cbz-piperidineHCID 21955499—
EduktN-(5-bromo-4-chloropyridin-2-yl)-2,2-dimethylpropanamideHCID 59613421—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
ProduktBenzyl 4-((5-bromo-2-pivalamidopyridin-4-ylamino)methyl)piperidine-1-carboxylateHCID 5961349287,2%

Reaktionsbedingungen

Temperatur210 °C

Reaktionsschritte

Two capped microwave reaction vials each containing a solution of N-(5-bromo-4-chloropyridin-2-yl)pivalamide (0.55 g, 1.89 mmol), benzyl 4-(aminomethyl)piperidine-1-carboxylate (1.07 g, 2 eq.) and triethylamine (0.80 mL, 3 eq.) in NMP (3.8 mL) were heated at 210° C. by microwave irradiation for 1.5 hr and then allowed to cool. The contents of the two vials were combined and partitioned between EtOAc (15 mL) and sat. NaHCO3 (150 mL). The organic layer was retained whilst the aqueous was further extracted with EtOAc (15 mL). The organic extracts were combined, washed with brine (50 mL), dried (MgSO4) and concentrated. The crude material was purified by chromatography on a 40+M Biotage silica column, eluting with a gradient of EtOAc in dichloromethane, to give the title compound as a clear oil (0.83 g, 43%)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08367658B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-a00b10751029486d80d9e3dfdd8c6e3b
Quellennotizuspto-grants-2013_02