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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 401493Erstellt: 26. Oktober 2026

Potassium Carbonate → Tert-butyl 4-(6-(2-amino-5-bromonicotinoyl)pyridin-2-yl)-1,4-diazepane-1-carboxylate

https://huagongshe.com/reaction/401493

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktTert-butyl 1,4-diazepane-1-carboxylateHCID 2756058—
Edukt(2-Amino-5-bromopyridin-3-yl)(6-fluoropyridin-2-yl)methanoneHCID 57690795—
LösungsmittelDimethylformamideHCID 6228—
ProduktTert-butyl 4-(6-(2-amino-5-bromonicotinoyl)pyridin-2-yl)-1,4-diazepane-1-carboxylateHCID 5769060159%

Reaktionsbedingungen

Temperatur95 °C

Reaktionsschritte

A mixture of (2-amino-5-bromopyridin-3-yl)(6-fluoropyridin-2-yl)methanone (190 mg, 0.64 mmol), 1-Boc-homopiperazine (0.14 ml, 0.70 mmol) and potassium carbonate (310 mg, 2.24 mmol) in dimethylformamide (4 ml) was heated at 95° C. for 48 hours. The reaction mixture was cooled down to room temperature and concentrated in vacuo. The residue was slurried in EtOAc and K2CO3 was filtered off. The mother liquors were concentrated in vacuo. The resulting residue was purified on silica gel by flash column chromatography (ISCO Companion|, 12 g column, 0-20% EtOAc/Petrol) to give the title compound as a yellow solid (180 mg, 59% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08741931B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-776fe7358e5843018ec47bbae2422edb
Quellennotizuspto-grants-2014_06