Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1696103Erstellt: 25. Oktober 2026

1,2,4-Thiadiazol-5-amine--hydrogen chloride (1/1) → 4-(2-Oxo-4-(2,2,2-trifluoroacetyl)piperazin-1-yl)-n-(1,2,4-thiadiazol-5-yl)benzenesulfonamide

https://huagongshe.com/reaction/1696103

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2,4-Thiadiazol-5-amine--hydrogen chloride (1/1)HCID 22014543—
EduktHCID 59465974HCID 59465974—
LösungsmittelPyridineHCID 1049—
Produkt4-(2-Oxo-4-(2,2,2-trifluoroacetyl)piperazin-1-yl)-n-(1,2,4-thiadiazol-5-yl)benzenesulfonamideHCID 5946640248%

Reaktionsschritte

Synthesized according to general procedure 12, method A. The reaction was set up with 1,2,4-Thiadiazol-5-ylamine hydrochloride (0.56 g, 4.0 mmol), anhydrous pyridine (3.5 mL), and 4-(2-oxo-4-(2,2,2-trifluoroacetyl)piperazin-1-yl)benzene-1-sulfonyl chloride (1.5 g, 4.0 mmol). The dark oil was purified via silica gel chromatography using 5% MeOH in CH2Cl2 followed by a second purification on silica gel using 80% EtOAc in hexanes to obtain the desired sulfonamide as a white solid (0.73 g, 1.92 mmol, 48% yield). LC/MS (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)), m/z: M+1 obs=436.1; tR=2.27 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08163720B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-d6c00f8373474349ae3194d58c284a01
Quellennotizuspto-grants-2012_04