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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1528341Erstellt: 27. Oktober 2026

Potassium Iodide → (Z)-N-[(2-amino-1,3-thiazol-4-yl)methoxy]benzenecarboximidoyl cyanide

https://huagongshe.com/reaction/1528341

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktCesium carbonateHCID 10796—
Edukt2-Thiazolamine, 4-(chloromethyl)-, hydrochloride (1:1)HCID 73228—
EduktN-Hydroxybenzimidoyl cyanideHCID 5464219—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelAcetonitrileHCID 6342—
Produkt(Z)-N-[(2-amino-1,3-thiazol-4-yl)methoxy]benzenecarboximidoyl cyanideHCID 8944388290%

Reaktionsschritte

To a solution of (2Z)-(hydroxyimino)(phenyl)acetonitrile (2.5 g, 17.10 mmol, 1 eq.) in 100 ml of acetonitrile and 10 ml DMF was added 4-(chloromethyl)-1,3-thiazol-2-amine hydrochloride (3.79 g, 20.52 mmol, 1.2 eq.) followed by potassium iodide (283 mg, 1.71 mmol, 0.1 eq.) and caesium carbonate (13.37 g, 41.05 mmol, 2.4 eq.). The reaction was stirred overnight at room temperature. The solvent was then evaporated and the residue dissolved in EtOAc (100 ml). The organic layer was washed with H2O and dried over MgSO4 then concentrated. (2Z)-{[(2-amino-1,3-thiazol-4-yl)methoxy]imino}(phenyl)acetonitrile (4 g, 90% yield, only 1 oxime isomer) was obtained as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09090600B2
Quelldatensatzuspto-grants-2015_07
ORD IDord-b941f558737340e3a36bf5c68caf4ba2
Quellennotizuspto-grants-2015_07