Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 78371Erstellt: 24. Oktober 2026

2-Morpholinoethylamine → 3-(4-Nitrophenoxy)benzoic acid

https://huagongshe.com/de/reaction/78371

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-MorpholinoethylamineHCID 408285—
Edukt3-(4-Nitrophenoxy)benzoic acidHCID 767919—
Produkt3-(4-Nitrophenoxy)benzoic acidHCID 767919—
ProduktN-[2-(4-morpholinyl)ethyl]-3-(4-nitrophenoxy)benzamideHCID 66745649—

Reaktionsschritte

Entry 61: 4-(3-Carboxyphenoxy)-1-nitrobenzene was synthesized according to Method A13, Step 2. 4-(3-Carboxyphenoxy)-1-nitrobenzene was coupled with 4-(2-aminoethyl)morpholine according to Method A13, Step 3 to give 4-(3-(N-(2-morpholinylethyl)carbamoyl)phenoxy)-1-nitrobenzene. According to Method A13 Step 4, 4-(3-(N-(2-morpholinylethyl)carbamoyl)phenoxy)-1-nitrobenzene was reduced to 4-(3-(N-(2-morpholinylethyl)carbamoyl)phenoxy)aniline. According to Method C1a, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(3-(N-(2-morpholinylethyl)carbamoyl)phenoxy)aniline to afford the urea.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841330B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-4b915e102afe45c180e79fc45a756656
Quellennotizuspto-grants-2014_09