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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 133738Erstellt: 25. Oktober 2026

n-(2-Fluoro-4-hydroxyphenyl)acetamide → (2S)-3-(4-Acetylamino-3-fluorophenoxy)-2-hydroxy-2-methyl-N-(3-methyl-4-nitrophenyl)propionamide

https://huagongshe.com/reaction/133738

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktn-(2-Fluoro-4-hydroxyphenyl)acetamideHCID 190616—
Edukt(2R)-3-bromo-2-hydroxy-2-methyl-N-(3-methyl-4-nitrophenyl)propionamideHCID 59903827—
Produkt(2S)-3-(4-Acetylamino-3-fluorophenoxy)-2-hydroxy-2-methyl-N-(3-methyl-4-nitrophenyl)propionamideHCID 67526766—

Reaktionsschritte

(2S)-3-(4-Acetylamino-3-fluorophenoxy)-2-hydroxy-2-methyl-N-(3-methyl-4-nitrophenyl)propionamide was prepared according to the method B as described in Example 3e starting from 4-acetylamino-3-fluorophenol and N-[3-methyl-4-(nitro)phenyl]-(2R)-3-bromo-2-hydroxy-2-methylpropanamide. 1H NMR (DMSO-d6): 1.42 (3H, s), 2.02 (3H, s), 2.53 (3H, s), 3.97 (1H, d, J=9.7 Hz), 4.21 (1H, d, J=9.7 Hz), 6.23 (1H, bs), 6.72 (1H, m), 6.90 (1H, m), 7.56 (1H, m), 7.88 (1H, dd, J=9.0 Hz and 2.2 Hz), 7.93 (1H, d, J=2.2 Hz), 8.03 (1H, d, J=9.0 Hz), 9.51 (1H, s), 10.15 (1H, bs).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07390923B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-54a11b4223dc4a479215c80b33c67d28
Quellennotizuspto-grants-2008_06