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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711664Generated: October 30, 2026

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

https://huagongshe.com/reaction/711664

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) δ 1.54 (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 numberUS09181276B2
Source datasetuspto-grants-2015_11
ORD IDord-770e92b35c44427e96ca10a149fe00e9
Source noteuspto-grants-2015_11