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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 346491Erstellt: 24. Oktober 2026

Sodium Iodide → 5-Chloro-3-[(phenylthio)methyl]-1,2,4-thiadiazole

https://huagongshe.com/de/reaction/346491

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktThiophenolHCID 7969—
EduktSodium CarbonateHCID 10340—
Edukt5-Chloro-3-(chloromethyl)-1,2,4-thiadiazoleHCID 332610—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt5-Chloro-3-[(phenylthio)methyl]-1,2,4-thiadiazoleHCID 21081458—

Reaktionsschritte

1.05 eq of NaI were dissolved in dry acetone. 1 eq of 5-chloro-3-(chloromethyl)-1,2,4-thiadiazole, 1.03 eq of the thiophenol and 1 eq of Na2CO3 were added and the reaction mixture was stirred at ambient temperature for 2 hours. The reaction mixture was diluted with EtOAc and water. The organic phase was washed with an aqueous solution of Na2SO3 (sat), dried over MgSO4 and evaporated in vacuo. Preparative HPLC purification gave the 5-chloro-3-[(phenylthio)methyl]-1,2,4-thiadiazole. This was subsequently dissolved in 95% ethanol and conc. NH3 (aq) was added. In some cases acetonitrile was added in order to completely dissolve the starting material. The mixture was transferred to a microwave tube and run in the microwave at 150° C. for 5 min. the reaction was quenched with water and the desired 3-arylthiomethyl-5-amino-1,2,4-thiadiazole worked up and purified using standard procedures.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07173030B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-111ed844a99d4345a191b2cd24b48c9b
Quellennotizuspto-grants-2007_02