Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711770Generated: October 31, 2026

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

https://huagongshe.com/reaction/711770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl isocyanateHCID 78210—
Reactant2-Amino-4,5-dimethyl-thiophene-3-carbonitrileHCID 290236—
Solvent1,4-DioxaneHCID 31275—
ProductN-(3-cyano-4,5-dimethylthiophen-2-ylcarbamoyl)benzamideHCID 5745690284.7%

Reaction Steps

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+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181276B2
Source datasetuspto-grants-2015_11
ORD IDord-7930b066c1c841afb27051a523767858
Source noteuspto-grants-2015_11