HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonic Acid → 4-Carbamoylimidazolium 5-olate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonic Acid | HCID 7371 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | 2-Aminopropanediamide | HCID 96457 | — |
| Reactant | Hydroxybenzenesulfonic acid | HCID 15619088 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Benzenesulfonic Acid | HCID 7371 | — |
| Product | 4-Carbamoylimidazolium 5-olate | HCID 124343 | 82% |
Reaction Steps
Into a suspension of benzenesulfonic acid salt of 2-aminomalonamide [4] (1.20 g; 4.37 mmol) prepared above and benzenesulfonic acid monohydrate (81 mg; 0.46 mmol) in dry ethanol (100 ml) was added trimethyl orthoformate (1.9 ml; 17.4 mmol), and was refluxed for 2 hours under an argon atmosphere. The resulting white suspension was stirred overnight at room temperature and the precipitates were collected by filtration to give colorless benzenesulfonic acid salt of SM-108 (1.02 g; 3.58 mmol; yield 82%), which was identical with that obtained in Example 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08664405B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-89a35ac613174ff7ba10406a8b3ea7f5 |
| Source note | uspto-grants-2014_03 |