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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1356151Erstellt: 24. Oktober 2026

2-(Benzenesulfonyl)-3-phenyloxaziridine → 2-Amino-4-methanesulfinyl-6-phenoxy-pyrimidine-5-carbonitrile

https://huagongshe.com/de/reaction/1356151

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(Benzenesulfonyl)-3-phenyloxaziridineHCID 320405—
Edukt2-Amino-4-methylsulfanyl-6-phenoxy-pyrimidine-5-carbonitrileHCID 18507391—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Amino-4-methanesulfinyl-6-phenoxy-pyrimidine-5-carbonitrileHCID 1850734427%

Reaktionsschritte

To a stirred suspension of 950 mg (3.68 mmol) 2-amino-4-methylsulfanyl-6-phenoxy-pyrimidine-5-carbonitrile in 20 ml dichloromethane was added 3.84 g (14.7 mmol) 3-phenyl-2-(phenylsulfonyl)oxaziridine and stirring continued for 24 hours at room temperature. The reaction mixture was then concentrated in vacuo and the residue resuspended in ether/hexane and filtered to afford 270 mg (27%) 2-amino-4-methanesulfinyl-6-phenoxy-pyrimidine-5-carbonitrile as a light yellow crystalline solid. ES-MS m/e (%): 275 (M+H+, 100).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06586441B2
Quelldatensatzuspto-grants-2003_07
ORD IDord-33282ad0247142cab6529b07968f00c5
Quellennotizuspto-grants-2003_07