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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 471634Erstellt: 24. Oktober 2026

Benzoyl isocyanate → N-(3-cyano-4,5-dimethylthiophen-2-ylcarbamoyl)benzamide

https://huagongshe.com/de/reaction/471634

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl isocyanateHCID 78210—
Edukt2-Amino-4,5-dimethyl-thiophene-3-carbonitrileHCID 290236—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktN-(3-cyano-4,5-dimethylthiophen-2-ylcarbamoyl)benzamideHCID 5745690284,7%

Reaktionsschritte

To a solution of 2-amino-4,5-dimethylthiophene-3-carbonitrile (1680 g, 11.04 mol) in 1,4-dioxane (42 L) was added benzoylisocyanate (1624 g, 11.04 mol). The reaction mixture was then stirred at room temperature under nitrogen overnight. The resulting precipitate was collected by filtration, washed with 1,4-dioxane (3×1.7 l) and heptane (3×1.7 L), and dried under vacuum overnight to give N-(3-Cyano-4,5-dimethylthiophen-2-ylcarbamoyl)benzamide as a white solid (2800 g, 84.7% yield). 1H NMR (400 MHz, DMSO-d6) δ 2.10 (s, 3H), 2.24 (s, 3H), 7.52-7.56 (m, 2H), 7.64-7.69 (m, 1H), 8.01-8.03 (m, 2H), 11.57 (brs, 1H), 12.05 (brs, 1H). MS 300 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08633186B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-2a967f5d6e1a4e03a619985ce60fc982
Quellennotizuspto-grants-2014_01