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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 130741Erstellt: 25. Oktober 2026

Sodium borohydride → 6-{4-[(2-Cyclopentyl-ethylamino)-methyl]-phenoxy}-nicotinamide

https://huagongshe.com/reaction/130741

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium borohydrideHCID 4311764—
Edukt2-CyclopentylethanamineHCID 5305650—
Edukt6-(4-Formylphenoxy)pyridine-3-carboxamideHCID 56851422—
LösungsmittelMethanolHCID 887—
Produkt6-{4-[(2-Cyclopentyl-ethylamino)-methyl]-phenoxy}-nicotinamideHCID 5973026152,2%

Reaktionsschritte

Combine 6-(4-formyl-phenoxy)-nicotinamide (0.61 g, 2.54 mmol) with 2-Cyclopentyl-ethylamine (0.38 g, 3.3 mmol), 2 g of 3 {acute over (Å)} molecular sieves, and 10 mL of methanol. Stir for 18 h under nitrogen. Add sodium borohydride (0.5 g, 13.2 mmol), and stir for 24 h. Filter through Celite, remove the solvent in vacuo. Partition the residue between water (50 mL) and ethyl acetate (100 mL). Dry the organic phase (sodium sulfate), filter, and concentrate in vacuo. Adsorb on silica, and purify on an ISCO® 100 g system (eluting with 95:5:0.5 to 90:10:1 chloroform/ethanol/ammonium hydroxide) to afford 0.45 g of product. HPLC retention time: 5.93 min (98.7% purity), ESMS (M+): 340.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07381719B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-84f3d6a721274a9d824451f4301ec669
Quellennotizuspto-grants-2008_06