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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 78373Erstellt: 25. Oktober 2026

2-Aminomethyl-1-ethylpyrrolidine → 3-(4-Nitrophenoxy)benzoic acid

https://huagongshe.com/reaction/78373

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Aminomethyl-1-ethylpyrrolidineHCID 117295—
Edukt3-(4-Nitrophenoxy)benzoic acidHCID 767919—
Produkt3-(4-Nitrophenoxy)benzoic acidHCID 767919—
Produkt4-(3-(N-((1-methylpyrrolidinyl)methyl)carbamoyl)phenoxy)-1-nitrobenzeneHCID 23614564—

Reaktionsschritte

Entry 64: 4-(3-Carboxyphenoxy)-1-nitrobenzene was synthesized according to Method A13, Step 2. 4-(3-Carboxyphenoxy)-1-nitrobenzene was coupled with 2-aminomethyl-1-ethylpyrrolidine according to Method A13, Step 3 to give 4-(3-(N-((1-methylpyrrolidinyl)methyl)carbamoyl)phenoxy)-1-nitrobenzene. According to Method A13 Step 4, 4-(3-(N-((1-methylpyrrolidinyl)methyl)carbamoyl)phenoxy)-1-nitrobenzene was reduced to 4-(3-(N-((1-methylpyrrolidinyl)methyl)carbamoyl)phenoxy)aniline. According to Method C1a, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(3-(N-((1-methylpyrrolidinyl)methyl)carbamoyl)phenoxy)aniline to afford the urea.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841330B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-c5cc83a89151498694fca1031a7db691
Quellennotizuspto-grants-2014_09