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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1828168Erstellt: 26. Oktober 2026

N,O-Dimethylhydroxylamine → 2-Oxo-1-phenyl-2,3-dihydro-1H-benzoimidazole-5-carboxylic Acid Methoxy-methyl-amide

https://huagongshe.com/reaction/1828168

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,O-DimethylhydroxylamineHCID 14232—
Edukt3-Amino-4-phenylamino-benzoic acidHCID 773821—
Edukt4-Anilino-3-nitrobenzoic acidHCID 3824366—
EduktBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Oxo-1-phenyl-2,3-dihydro-1H-benzoimidazole-5-carboxylic Acid Methoxy-methyl-amideHCID 86587985—

Reaktionsschritte

To a stirred solution of 3-amino-4-phenylamino-benzoic acid (prepared from 3-nitro-4-phenylamino-benzoic acid as described in the general procedure, 2.04 gm, 8.94 mmol) in THF (25 mL) was added carbonyl diimidazole (3.62 gm, 22.34 mmol). After stirring for 1 hour at room temperature, N,O-dimethylhydroxyl amine (1.31 gm, 13.41 mmol) was added in one portion. Stirring was continued at room temperature for an additional 2 hours after which time the reaction was determined to be complete by LC-MS. The THF was removed in vacuo and the residue was diluted with water and extracted with methylene chloride three times. The combined methylene chloride extracts were dried over anhydrous sodium sulfate and concentrated in vacuo to afford 2.23 gm of the title compound as a tan solid which was used without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07056918B2
Quelldatensatzuspto-grants-2006_06
ORD IDord-700ef45fd088435ebd1e9349334f1ba8
Quellennotizuspto-grants-2006_06