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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 524988Erstellt: 25. Oktober 2026

Sodium Thiosulfate → 1-Amino-N-phenyl-1H-imidazole-2-carboxamide

https://huagongshe.com/reaction/524988

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ThiosulfateHCID 24477—
EduktSodium hydrideHCID 24758—
EduktDiphenylphosphinamideHCID 853560—
EduktN-phenyl-1H-imidazole-2-carboxamideHCID 2822525—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-Amino-N-phenyl-1H-imidazole-2-carboxamideHCID 2110435276%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

0.430 g (10.75 mmol) of sodium hydride (60% dispersion in mineral oil) was added to a 0° C. cooled solution of N-phenyl-1H-imidazole-2-carboxamide (1.55 g, 8.27 mmol) in DMF (50 mL). The mixture was stirred at 0° C. for 30 minutes and 2.70 g (11.57 mmol) of DPPONH2 (P,P-diphenylphosphinic amide, available from Sigma Aldrich®, cat. no. 5994-87-6) were added portionwise. A thick suspension formed and additional 100 mL of DMF were added. The mixture was stirred at room temperature for 3 hours and then it was poured into 150 mL of a saturated aqueous solution of sodium thiosulphate and extracted with ethyl acetate. The combined organic layer was dried over sodium sulphate, filtered and concentrated. The crude product was purified by flash chromatography (20% to 40% AcOEt/Hexanes) to yield 1.27 g (76% yield) of the title compound as a pale yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09340547B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-d0cc1334dd974c8cafb4870783af19a5
Quellennotizuspto-grants-2016_05