HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiourea → HCID 22413713, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | HCID 10847027 | HCID 10847027 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22413713 | HCID 22413713 | 61.7% |
Reaction Steps
A suspension of 2-acetamidomethyl-5-chloroacetyl-3-methylfuran (24.8 g) and thiourea (8.2 g) in ethanol (250 ml) was stirred at room temperature for 2 hours. The resulting precipitate was collected by filtration and then dissolved in water (200 ml). The mixture was alkalized with an aqueous potassium carbonate solution. The resulting precipitate was collected by filtration to afford 4-(5-acetylaminomethyl-4-methylfuran-2-yl)-2-aminothiazole (16.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05512588 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-0c895d5b01104be187a751a883af90f6 |
| Source note | uspto-grants-1996_04 |