HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → N-(2-Cyano-4-phenylphenyl)sulfamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | N-(2-cyano-4-bromophenyl)sulfamide | HCID 67402187 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Water 1,2-dimethoxyethane | HCID 18180031 | — |
| Product | N-(2-Cyano-4-phenylphenyl)sulfamide | HCID 67400461 | — |
Reaction Steps
In a 2 mL microwave vial, phenyl boronic acid (75 mg, 0.6 mmol), N-(2-cyano-4-bromophenyl)sulfamide (Example 83b) (137 mg, 0.5 mmol), and potassium carbonate (400 mg, 1.5 mmol) were dissolved in DME/Water mixture (1.5 mL, DME/Water 4:1). The solution was degassed by bubbling N2 gas into the reaction solution for 5 minutes and Palladium tetrakis triphenylphospine (25 mg, 0.025 mmol) was added. The reaction was placed in a microwave reactor for 5 minutes at 150° C. The crude reaction was dissolved in water and washed with ethyl acetate. The aqueous solution was evaporated under vacuum to give N-(2-Cyano-4-phenylphenyl)sulfamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08633186B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-3dc0644542a34810bc4b05796c461dcd |
| Source note | uspto-grants-2014_01 |