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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29600Erstellt: 24. Oktober 2026

(2-Amino-5-chloro-phenyl)-(2-methyl-pyridin-3-yl)-methanone → 3-(4-[4-Chloro-2-(2-methyl-pyridine-3-carbonyl)-phenylsulfamoyl]-phenyl)-propionic acid methyl ester

https://huagongshe.com/de/reaction/29600

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(2-Amino-5-chloro-phenyl)-(2-methyl-pyridin-3-yl)-methanoneHCID 22327321—
EduktMethyl 3-[4-(chlorosulfonyl)phenyl]propanoateHCID 23158517—
Produkt3-(4-[4-Chloro-2-(2-methyl-pyridine-3-carbonyl)-phenylsulfamoyl]-phenyl)-propionic acid methyl esterHCID 10027807—

Reaktionsschritte

The title compound was prepared according to the general procedure for the synthesis of N-Aryl-benzenesulfonamides previously described using (2 amino-5-chloro-phenyl)-(2-methyl-pyridin-3-yl)-methanone and 3-(4-Chlorosulfonyl-phenyl)-propionic acid methyl ester and purified by HPLC. 1H-NMR (CDCl3) δ 10.75 (br s, 1H, NH), 8.64 (dm, 1H, J=4.8 Hz), 7.79 (dd, 1H, J=9.2 Hz, J=1.1 Hz), 7.75 (d, 2H, J=7.3 Hz), 7.49 (dm, 1H,J=9.2 Hz), 7.1-7.3 (m, 5H), 3.65 (s, 3H), 2.97(t, 2H, J=7.6 Hz), 2.61 (t, 2H, J=7.6 Hz), 2.35 (s, 3H). MS: m/z 473 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07420055B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-391c4fec674349d6bc9dbb6fd0e54d75
Quellennotizuspto-grants-2008_09