HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559827Generated: October 25, 2026
2-Aminothiazole → 1-(2-Phenoxyphenyl)-5-(thiazol-2-yl)biuret
https://huagongshe.com/reaction/559827
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Benzenamine, 2-phenoxy- | HCID 75899 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Isocyanatocarbonyl chloride | HCID 119708 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2-Phenoxyphenyl)-5-(thiazol-2-yl)biuret | HCID 59733035 | 55.3% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08063081B2 |
|---|
| Source dataset | uspto-grants-2011_11 |
|---|
| ORD ID | ord-d34249aca5d74c04a60c3bc5072a013a |
|---|
| Source note | uspto-grants-2011_11 |
|---|