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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 228152Erstellt: 23. Oktober 2026

2-Methoxybenzaldehyde → 6-{4-[2-(2-Methoxy-benzylamino)-ethyl]-phenoxy}-nicotinamide

https://huagongshe.com/de/reaction/228152

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-MethoxybenzaldehydeHCID 8658—
EduktSodium borohydrideHCID 4311764—
Edukt6-[4-(2-Amino-ethyl)-phenoxy]-nicotinamideHCID 59730017—
LösungsmittelMethanolHCID 887—
Produkt6-{4-[2-(2-Methoxy-benzylamino)-ethyl]-phenoxy}-nicotinamideHCID 5973039685,4%

Reaktionsschritte

Add three-angstrom molecular sieves to a stirred solution of 6-[4-(2-amino-ethyl)-phenoxy]-nicotinamide (0.1000 g, 0.3887 mmol) (compound of example 33), 2-methoxybenzaldehyde (0.047 mL, 0.39 mmol), and methanol (5 mL). Agitate the reaction for 18 h on a platform shaker at room temperature. Add sodium borohydride and agitate for 1 h at room temperature. Filter to remove the molecular sieves and load the reaction mixture directly onto a 10 g prepacked SCX cartridge. Flush with methanol (150 mL) and elute the product off the SCX cartridge with 2 M ammonia in methanol (50 mL). Concentrate on a rotary evaporator to give 0.1253 g (85%) of 6-{4-[2-(2-methoxy-benzylamino)-ethyl]-phenoxy}-nicotinamide: HPLC (30/70 to 90/10 ACN/(0.1% TFA in water) Zorbax SB-Phenyl Column 4.6 mm×15 cm×5 micron: Retention time: 4.14 minutes, Purity: 97.9%; mass spectrum (ion spray): m/z=378.1 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07560463B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-b3acef7e9e4a4039970a72a40a2eb3ff
Quellennotizuspto-grants-2009_07