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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2266403Erstellt: 25. Oktober 2026

5-Cyclopropyl-1,3,4-thiadiazol-2-amine → 5-Chloro-N-{2-[4-(5-cyclopropyl-[1,3,4]thiadiazol-2-ylsulfamoyl)-phenyl]-ethyl}-2-methoxy-benzamide

https://huagongshe.com/reaction/2266403

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-Cyclopropyl-1,3,4-thiadiazol-2-amineHCID 717021—
Edukt4-(2-((5-Chloro-2-methoxyphenyl)formamido)ethyl)benzene-1-sulfonyl chlorideHCID 4454576—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelPyridineHCID 1049—
Produkt5-Chloro-N-{2-[4-(5-cyclopropyl-[1,3,4]thiadiazol-2-ylsulfamoyl)-phenyl]-ethyl}-2-methoxy-benzamideHCID 5758681842,2%

Reaktionsbedingungen

Temperatur115 °C

Reaktionsschritte

1.1 g 4-[2-(5-Chloro-2-methoxy-benzoylamino)-ethyl]-benzenesulfonyl chloride, 483 mg 5-Cyclopropyl-[1,3,4]thiadiazol-2-ylamine and 35.0 mg 4-dimethylaminopyridine were dissolved in 5 ml pyridine and stirred under microwave irradiation at 115° C. for two hours. The pyridine was removed in vacuo and the residue coevaporated three times with portions of 20 ml toluene. The residue was purified by RP-HPLC to obtain 590 mg 5-Chloro-N-{2-[4-(5-cyclopropyl-[1,3,4]thiadiazol-2-ylsulfamoyl)-phenyl]-ethyl}-2-methoxy-benzamide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07858647B2
Quelldatensatzuspto-grants-2010_12
ORD IDord-f84d6dbf280d4bed969e5300335db827
Quellennotizuspto-grants-2010_12