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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 130740Erstellt: 26. Oktober 2026

Benzylamine → 6-(4-((Benzylamino)methyl)phenoxy)nicotinamide

https://huagongshe.com/reaction/130740

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzylamineHCID 7504—
EduktSodium borohydrideHCID 4311764—
Edukt6-(4-Formylphenoxy)pyridine-3-carboxamideHCID 56851422—
LösungsmittelMethanolHCID 887—
Produkt6-(4-((Benzylamino)methyl)phenoxy)nicotinamideHCID 44434949—

Reaktionsschritte

Combine 6-(4-Formyl-phenoxy)-nicotinamide (0.097 g, 0.4 mmol) in 5 mL of methanol with benzylamine (0.4 mmol), and 1 g of 3 {acute over (Å)} molecular sieves. Stir for 18 h. Add sodium borohydride (0.076 g, 2 mmol), and stir for 18 h. Flush the reactions down through a 5 g SCX column, first wash with 1:1 chloroform/methanol, then collect washes with 1:1 chloroform/2 M ammonia in methanol. Adsorb the collected material on silica, then purify via a ISCO® Combiflash 16× system (use a 10 g silica cartridge, and elute with 98:2:0.2 chloroform/ethanol/ammonium hydroxide, gradient to 90:10:1 chloroform/ethanol/ammonium hydroxide). 1H NMR (DMSO-d6): 8.58 (d, 1H), 8.22 (m, 1H), 8.0 (s, 1H), 7.46 (s, 1H), 7.27-7.38 (m, 6H), 7.20 (m, 1H) 7.02-7.08 (m, 3H), 3.67-3.68 (d, 4H). TLC Rf (90:10:1 chloroform/ethanol/ammonium hydroxide): 0.31.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07381719B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-1034da02824748b49c6038c43d83125b
Quellennotizuspto-grants-2008_06