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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1467963Erstellt: 25. Oktober 2026

Acetic Acid → Tert-butyl 4-((6-bromopyridin-3-yl)amino)piperidine-1-carboxylate

https://huagongshe.com/reaction/1467963

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt6-Bromopyridin-3-amineHCID 642811—
Edukttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
EduktSodium triacetoxyborohydrideHCID 5049666—
Lösungsmittel1,1-DichloroethaneHCID 6365—
LösungsmittelEthyl AcetateHCID 8857—
ProduktTert-butyl 4-((6-bromopyridin-3-yl)amino)piperidine-1-carboxylateHCID 8660214062%

Reaktionsschritte

To a mixture of tert-butyl 4-oxopiperidine-1-carboxylate (1.15 g, 5.78 mmol) and 6-bromopyridin-3-amine (0.5 g, 2.89 mmol) in dichloroethane (20 mL), acetic acid (8 mL, 2.89 mmol) was added and the contents were stirred at room temperature for 3 h. Sodium triacetoxy borohydride (1.225 g, 5.78 mmol) was added and the contents were stirred at room temperature for 12 h. The reaction was diluted with ethyl acetate and washed with brine; the organic layer was separated and concentrated in vacuo. The resulting residue was purified by flash column chromatography to give tert-butyl 4-((6-bromopyridin-3-yl)amino)piperidine-1-carboxylate (0.638 g, 62%); MS: 357.1 (M+1)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09000175B2
Quelldatensatzuspto-grants-2015_04
ORD IDord-095a9df2de08454da67543e86e1307a9
Quellennotizuspto-grants-2015_04