HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101211Generated: October 30, 2026
Sodium Bicarbonate → 2-[(Aminocarbonyl)amino]-5-[4-formylphenyl]thiophene-3-carboxamide
https://huagongshe.com/reaction/2101211
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Formylphenylboronic Acid | HCID 591073 | — |
| Reactant | 5-Bromo-2-ureidothiophene-3-carboxamide | HCID 11184626 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-[(Aminocarbonyl)amino]-5-[4-formylphenyl]thiophene-3-carboxamide | HCID 21914326 | 44.7% |
Reaction Steps
2-[(Aminocarbonyl)amino]-5-bromothiophene-3-carboxamide (11.75 g) was stirred in DME (500 ml) and saturated aqueous sodium bicarbonate solution (100 ml), and 4-formylphenyl boronic acid (10 g) was added. The flask was flushed with argon and tetrakis-(triphenylphosphine)palladium(0) (5.1 g) was then added. The reaction was stirred at 90° C. for 2 h, then cooled and evaporated under reduced pressure. The residue was treated with DCM (200 ml) and 2N sodium hydroxide solution (100 ml), and stirred for 20 min. The resulting solid was then isolated by filtration and purified by trituration with ethanol (100 ml), giving the product as a pale green solid (5.75 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07572826B2 |
|---|
| Source dataset | uspto-grants-2009_08 |
|---|
| ORD ID | ord-b66632cd96044e95b05907e89d5e4266 |
|---|
| Source note | uspto-grants-2009_08 |
|---|