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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1269777Erstellt: 27. Oktober 2026

Ammonium formate → N-methyl-N-piperidin-4-yl-1H-indazole-5-carboxamide

https://huagongshe.com/reaction/1269777

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium formateHCID 2723923—
EduktN-(1-benzylpiperidin-4-yl)-N-methyl-1H-indazole-5-carboxamideHCID 22933863—
KatalysatorPalladiumHCID 23938—
LösungsmittelEthanolHCID 702—
ProduktN-methyl-N-piperidin-4-yl-1H-indazole-5-carboxamideHCID 2293351277%

Reaktionsschritte

Ammonium formate (400 mg) and 10%-Pd/C (80 mg) were added to a solution of the N-(1-benzylpiperidin-4-yl)-N-methyl-1H-indazole-5-carboxamide (435.1 mg, 1.25 mmol) obtained in Example 318 in ethanol (10 ml) at room temperature, and the resulting mixture was refluxed for 2 hours. The reaction mixture was filtered by the use of Celite, and the filtrate was concentrated and the resulting residue was purified by a silica gel column chromatography (eluent: chloroform/methanol (1%-aqueous ammonia)) to obtain N-methyl-N-piperidin-4-yl-1H-indazole-5-carboxamide (247 mg, 77%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07199147B2
Quelldatensatzuspto-grants-2007_04
ORD IDord-34e6e0b633e6476a8dd86e3e4ab6ba50
Quellennotizuspto-grants-2007_04