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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 69880Erstellt: 24. Oktober 2026

1,2-Dichloroethane → Tert-butyl 1-(3-(3-amino-6-bromopyrazine-2-carboxamido)pyridin-4-yl)piperidin-3-ylcarbamate

https://huagongshe.com/de/reaction/69880

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
EduktHOAtHCID 181649—
Edukt3-Amino-6-bromopyrazine-2-carboxylic acidHCID 18521600—
EduktTert-butyl 1-(3-aminopyridin-4-yl)piperidin-3-ylcarbamateHCID 67130164—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
ProduktTert-butyl 1-(3-(3-amino-6-bromopyrazine-2-carboxamido)pyridin-4-yl)piperidin-3-ylcarbamateHCID 86669179—

Reaktionsschritte

A solution containing 1 eq each of tert-butyl 1-(3-aminopyridin-4-yl)piperidin-3-ylcarbamate, 3-amino-6-bromopyrazine-2-carboxylic acid, HOAT and EDC in DMF, at a concentration of 0.5 M, was stirred for 60 hours. The solution was diluted with EtOAc and was washed with H2O (4×), NaCl(sat.), was dried over MgSO4, was filtered and the volatiles were removed in vacuo. After purification by silica gel chromatography (EtOAc eluant), tert-butyl 1-(3-(3-amino-6-bromopyrazine-2-carboxamido)pyridin-4-yl)piperidin-3-ylcarbamate was obtained (78%). LCMS (m/z): 492.2 (MH+); LC Rt=2.68 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822497B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-9592b42608d044f0b3167cbee937b637
Quellennotizuspto-grants-2014_09