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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1929382Erstellt: 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/1929382

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—
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 dimethylfonmamide (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
PatentnummerUS08188071B2
Quelldatensatzuspto-grants-2012_05
ORD IDord-151ccf1347bc48faa50a3c82a186443d
Quellennotizuspto-grants-2012_05