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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 38139Erstellt: 25. Oktober 2026

Oxalyl chloride → N-[(5-chloro(2-thienyl))sulfonyl]-N'-[4-(5-chloro-1,3-dioxobenzo [c]azolidin-2-yl)-3-methylphenyl]ethane-1,2-diamide

https://huagongshe.com/reaction/38139

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxalyl chlorideHCID 65578—
EduktN-(4-Amino-o-tolyl)-4-chlorophthalimideHCID 93991—
Edukt5-Chlorothiophene-2-SulfonamideHCID 1241301—
ProduktN-[(5-chloro(2-thienyl))sulfonyl]-N'-[4-(5-chloro-1,3-dioxobenzo [c]azolidin-2-yl)-3-methylphenyl]ethane-1,2-diamideHCID 2080025744%

Reaktionsschritte

A 200 mg (1.0 mmol) of 5-chlorothiophenesulfonamide was slurried in 0.5 mL of oxalyl chloride and refluxed for 6 h. The solvent was removed in vacuo and 36 mg of the resulting solid was dissolved in 240 μL acetonitrile and treated with 40 mg (0.14 mmol) 2-(4-amino-2-methylphenyl)-5-chlorobenzo[c]azoline-1,3-dione. After stirring for 1 h, the solvent was removed and the residue was purified by RP-HPLC to give 33 mg (44%) of the titled compound. ES-MS (M+H)+=538(2Cl).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524721B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-9ec4754677b44b32a431031ad2edb79d
Quellennotizuspto-grants-2013_09