HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 3-[(Aminocarbonyl)amino]-5-(3-hydroxyphenyl)-2-thiophenecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Trimethylsilyl isocyanate | HCID 70696 | — |
| Reactant | 3-Amino-5-(3-methoxyphenyl)-2-thiophenecarboxamide | HCID 9964869 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-[(Aminocarbonyl)amino]-5-(3-hydroxyphenyl)-2-thiophenecarboxamide | HCID 9965424 | — |
Reaction Steps
3-Amino-5-(3-methoxyphenyl)-2-thiophenecarboxamide (0.5 g), trimethylsilylisocyanate (2 mL), dimethylformamide (2 mL) and dichloromethane were heated at reflux for 3 days. After cooling the solid was filtered off, suspended in dichloromethane (100 mL) and treated with boron tribromide (5 mL of a 1M solution in dichloromethane). After 3 days. methanol (50 mL) was added. After 1 h, the solvent was evaporated and the residue was triturated with 2M hydrochloric acid. The title urea was filtered off (0.35 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07358376B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-cd440d8d0d8f4e91977ddd3af6825c5c |
| Source note | uspto-grants-2008_04 |