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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1485579Erstellt: 25. Oktober 2026

Potassium Carbonate → tert-Butyl (1-pyridazin-3-ylpiperidin-4-yl)carbamate

https://huagongshe.com/reaction/1485579

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktCesium fluorideHCID 25953—
Edukt4-(N-Boc-amino)piperidineHCID 723833—
Edukt3-BromopyridazineHCID 13126699—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkttert-Butyl (1-pyridazin-3-ylpiperidin-4-yl)carbamateHCID 8662587135,4%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

The reaction mixture of tert-butyl piperidin-4-ylcarbamate (250 mg, 1.25 mmol), 3-bromopyridazine (258 mg, 1.62 mmol), CsF (37.9 mg, 0.25 mmol), and K2CO3 (518 mg, 3.74 mmol) in DMSO (12.5 mL) was heated at 100° C. for 20 h. Water and DCM were poured into the mixture, and the separated aqueous layer was extracted with DCM, the combined organic layers were dried over Na2SO4, filtered, concentrated in vacuo. The residue was purified by column chromatography (Hexane:EtOAc=1:1) to give tert-butyl 1-(pyridazine-3-yl)piperidin-4-ylcarbamate (123 mg, 35%) as a pale yellow solid. 1H-NMR (CDCl3, Varian 400 MHz) δ 1.45 (9H, s), 1.92-2.12 (2H, m), 3.03-3.17 (2H, m), 3.55-3.80 (2H, m), 4.25-4.38 (2H, m), 4.52 (1H, brs), 6.92 (1H, d, J=9.2 Hz), 7.20 (1H, dd, J=4.4, 9.2 Hz), 8.56 (1H, d, J=4.4 Hz). NH peak was not observed. m/z=279.06 [M+1]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09422298B2
Quelldatensatzuspto-grants-2016_08
ORD IDord-23525637b4f04fb6a18f2c15dd65498f
Quellennotizuspto-grants-2016_08