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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 602087Erstellt: 25. Oktober 2026

Potassium Carbonate → N-[1-(2-Cyclopropyl-1-methylethyl)piperidin-4-yl]-6-(3-fluorophenyl)nicotinamide

https://huagongshe.com/reaction/602087

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt1-Cyclopropylpropan-2-oneHCID 537025—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt6-(3-fluorophenyl)-N-(piperidin-4-yl)nicotinamideHCID 67267906—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelEthanolHCID 702—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-[1-(2-Cyclopropyl-1-methylethyl)piperidin-4-yl]-6-(3-fluorophenyl)nicotinamideHCID 59743699—

Reaktionsschritte

To a solution of 1-cyclopropylpropan-2-one (0.2 mL, 0.08 mmol in 1:1 THF:DMSO) was added 6-(3-fluorophenyl)-N-(piperidin-4-yl)nicotinamide (in 1:1 THF:DMSO, 0.2 mL, 0.08 mmol), sodium triacetoxyborohydride dispersion (0.33 mL, 2.5 eq, in 1:1 THF:DMSO) and glacial acetic acid (0.01 mL). The reaction mixture was stirred at room temperature for 16-24 h and then aqueous K2CO3 (3 M, 0.2 mL) and ethanol (0.55 mL) was added. The reaction was shaken for 30 min and then the mixture was filtered and the filtrate concentrated and the residue purified by RP-HPLC to give the desired product. LC/MS=382.4 (M+H) observed, 382.23 expected.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07902373B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-3768ad9dae2347b9ab440a2bbb884ccf
Quellennotizuspto-grants-2011_03