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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29605Erstellt: 23. Oktober 2026

(2-Amino-5-chloro-phenyl)-(6-methyl-pyridin-3-yl)methanone → 3-{4-[4-Chloro-2-(6-methyl-pyridine-3-carbonyl)-phenylsulfamoyl]-phenyl}-propionic acid methyl ester

https://huagongshe.com/de/reaction/29605

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(2-Amino-5-chloro-phenyl)-(6-methyl-pyridin-3-yl)methanoneHCID 22327305—
EduktMethyl 3-[4-(chlorosulfonyl)phenyl]propanoateHCID 23158517—
Produkt3-{4-[4-Chloro-2-(6-methyl-pyridine-3-carbonyl)-phenylsulfamoyl]-phenyl}-propionic acid methyl esterHCID 10322607—

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)-(6-methyl-pyridin-3-yl)-methanone and 3-(4-Chlorosulfonyl-phenyl)-propionic acid methyl ester and purified by HPLC. 1H NMR (CDCl3) δ 9.66 (br s, 1H, NH), 8.34 (d, 1H, J=2.2 Hz), 7.75 (d, 1H, J=8.8 Hz), 7.72 (d, 1H, J=8.0 Hz, J=2.2 Hz), 7.56 (d, 2H, J=8.4 Hz), 7.51 (dd, 1H, J =8.8 Hz, J=2.2 Hz), 7.32 (d 1H, J=2.2 Hz), 7.26 (d, 1H, J=7 Hz), 7.09 (d, 2H, J=8.4 Hz), 3.65 (s, 3H), 2.97(t, 2H, J=7.6 Hz), 2.66 (s, 3H), 2.51 (t, 2H, J=7.6 Hz). MS: m/z 473 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07420055B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-ae256ad3b0b9401da6875972c652d264
Quellennotizuspto-grants-2008_09