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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 383616Erstellt: 25. Oktober 2026

Nitrogen → N-(3-Amino-phenyl)-3-(3,4,5-trimethoxy-phenyl)-propionamide

https://huagongshe.com/reaction/383616

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrogenHCID 947—
EduktN-(3-Nitro-phenyl)-3-(3,4,5-trimethoxy-phenyl)-propionamideHCID 9411047—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
ProduktN-(3-Amino-phenyl)-3-(3,4,5-trimethoxy-phenyl)-propionamideHCID 1622505499%

Reaktionsschritte

(The following reaction is done in an N2 atmosphere.) Dissolve N-(3-Nitro-phenyl)-3-(3,4,5-trimethoxy-phenyl)-propionamide (89) (100 mg, 0.28 mmol) in MeOH (4.5 mL) and add Pd on carbon (10% (w/w) Pd content, 29.5 mg, 0.028 mmol) followed by NH4CO2H (175 mg, 2.77 mmol) at rt. Degas the reaction mixture carefully (flush with N2) and stir it for 75 min at rt. Filtrate reaction mixture through a short pad of celite and remove solvent. Treat residue with EtOAc, filtrate again through a short pad of celite and remove solvent to obtain N-(3-Amino-phenyl)-3-(3,4,5-trimethoxy-phenyl)-propionamide (90) (91 mg, 99%) as a white solid. No further purification. 1H NMR (400 MHz, CD3OD): 2.65 (t, 2H, J=7.5 Hz); 2.98 (t, 2H, J=7.5 Hz); 3.75 (s, 3H); 3.82 (s, 6H); 6.50 (dd, 1H, J1=8.0 Hz, J2=2.0 Hz); 6.58 (s, 2H); 6.80 (dd, 1H, J=8.0 Hz, J2=2.0 Hz); 7.02-7.07 (m, 1H); 7.04 (t, 1H, J=8.0 Hz).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08367677B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-9ede8fb8e0f041c595165695f309931d
Quellennotizuspto-grants-2013_02