HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 1,2,4-Thiadiazol-5-amine--hydrogen chloride (1/1) | HCID 22014543 | — |
| Edukt | HCID 59465974 | HCID 59465974 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | 4-(2-Oxo-4-(2,2,2-trifluoroacetyl)piperazin-1-yl)-n-(1,2,4-thiadiazol-5-yl)benzenesulfonamide | HCID 59466402 | 48% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08163720B2 |
| Quelldatensatz | uspto-grants-2012_04 |
| ORD ID | ord-d6c00f8373474349ae3194d58c284a01 |
| Quellennotiz | uspto-grants-2012_04 |