HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 598912Erstellt: 25. Oktober 2026
2-Aminothiazole → 1-(2-Phenoxyphenyl)-5-(thiazol-2-yl)biuret
https://huagongshe.com/reaction/598912
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Aminothiazole | HCID 2155 | — |
| Edukt | Benzenamine, 2-phenoxy- | HCID 75899 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | Isocyanatocarbonyl chloride | HCID 119708 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-(2-Phenoxyphenyl)-5-(thiazol-2-yl)biuret | HCID 59733035 | 55,3% |
Reaktionsschritte
To a solution of 2-phenoxyaniline (0.46 g, 2.50 mmol) in tetrahydrofuran (20 ml) was added diisopropylethylamine (0.89 ml, 5.00 mmol) and the solution was cooled to −30° C., then N-(chlorocarbonyl)isocyanate (0.3 ml, 3.75 mmol) was slowly added. The mixture was then allowed to warm up to the room temperature during 30 min. 2-Aminothiazole (0.375 g, 3.75 mmol) was added to the reaction mixture and stirred at room temperature for 6 hours. The reaction mixture was concentrated under reduced pressure to afford crude product, which was purified by silica gel chromatography (hexanes:ethyl acetate from 80:20 to 30:70) to afford title compound (0.49 g, 55%) as pale yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07897628B2 |
|---|
| Quelldatensatz | uspto-grants-2011_03 |
|---|
| ORD ID | ord-3dac87a570b6488e8231d9879114e80b |
|---|
| Quellennotiz | uspto-grants-2011_03 |
|---|