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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167822Generated: November 2, 2026

Cyanamide → 2-(4-Aminosulfonylphenyl)amino-4-amino-thiazole-5-carbonitrile

https://huagongshe.com/reaction/1167822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanamideHCID 9864—
ReactantBromoacetonitrileHCID 11534—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant4-IsothiocyanatobenzenesulfonamideHCID 521359—
SolventAcetonitrileHCID 6342—
Product2-(4-Aminosulfonylphenyl)amino-4-amino-thiazole-5-carbonitrileHCID 2299391849.4%

Reaction Steps

To a solution of 4-(aminosulfonyl)phenylisothiocyanate (1.12 g, 5.0 mmol) and cyanamide (0.23 g, 5.5 mmol) in acetonitrile (50 ml) was added DBU (0.83 g, 5.5 mmol), and the resulting mixture was stirred at room temperature for 60 minutes. To the reaction mixture was added bromo-acetonitrile (0.66 g, 5.5 mmol) followed by DBU (0.83 g, 5.5 mmol) 30 minutes afterward. The reaction mixture was stirred overnight at room temperature, the solvent was removed at the reduced pressure, and the residue was dissolved in EtOAc (200 ml). The EtOAc solution was washed with 0.1 N HCl (150 ml×3) and brine and dried with MgSO4 and concentrated. The residue was purified by silica gel chromatography (EtOAc) to provide 0.73 g (48%) of 2-(4-aminosulfonylphenyl)amino-4-amino-thiazole-5-carbonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620828B2
Source datasetuspto-grants-2003_09
ORD IDord-a846c747fc21416ebcf8cc3c852d28d7
Source noteuspto-grants-2003_09