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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyanamide | HCID 9864 | — |
| Reactant | Bromoacetonitrile | HCID 11534 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 4-Isothiocyanatobenzenesulfonamide | HCID 521359 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(4-Aminosulfonylphenyl)amino-4-amino-thiazole-5-carbonitrile | HCID 22993918 | 49.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06620828B2 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-a846c747fc21416ebcf8cc3c852d28d7 |
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| Source note | uspto-grants-2003_09 |
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