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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44395Generated: October 30, 2026

Benzoyl isocyanate → Tert-butyl 5-(3-benzoylureido)-4-cyano-3-methylthiophene-2-carboxylate

https://huagongshe.com/reaction/44395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl isocyanateHCID 78210—
ReactantHCID 18445366HCID 18445366—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductTert-butyl 5-(3-benzoylureido)-4-cyano-3-methylthiophene-2-carboxylateHCID 5745693384.2%

Reaction Steps

To a solution of tert-butyl 5-amino-4-cyano-3-methylthiophene-2-carboxylate (example 64b) (16 g, 67.14 mmol) in dioxane (200 mL), was added benzoyl isocyanate (10 g, 67.14 mmol). The reaction mixture was stirred at rt overnight, and upon completion was diluted with EtOAc, washed with NaHCO3, water, brine, dried over MgSO4, filtered and concentrated to yield tert-butyl 5-(3-benzoylureido)-4-cyano-3-methylthiophene-2-carboxylate (21.78 g, 84%) as a brown solid. 1H NMR (400 MHz, DMSO-d6) δ1.54 (s, 9H), 3.58 (s, 3H), 7.58 (t, J=7.5 Hz, 2H), 7.71 (t, J=7.5 Hz, 1H), 7.88 (d, J=7.5 Hz, 1H), 8.05 (d, J=7.5 Hz, 2H), 12.25 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541421B2
Source datasetuspto-grants-2013_09
ORD IDord-ead60eac00644ee3a37bc708d3093910
Source noteuspto-grants-2013_09