HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262896Generated: November 2, 2026
Dimethylformamide → Tert-butyl 4-(4-phenyl-1,3-thiazol-2-yl)piperazine-1-carboxylate
https://huagongshe.com/reaction/2262896
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 2-Chloro-4-phenylthiazole | HCID 2761359 | — |
| Solvent | Water | HCID 962 | — |
| Product | Tert-butyl 4-(4-phenyl-1,3-thiazol-2-yl)piperazine-1-carboxylate | HCID 68777857 | — |
Reaction Steps
A mixture of 2-chloro-4-phenyl-1,3-thiazole (1.16 g, 5.92 mmol), 1-(tert-butoxycarbonyl)-piperazine (3.30 g, 17.8 mmol), potassium carbonate (817 mg, 5.92 mmol) and N,N-dimethylformamide (20 ml) was stirred at 120° C. for 2 hours, poured to water, which was extracted with ethyl acetate. The extract was washed with water, dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=7:3) to give the desired product as a solid. The resulting solid was recrystallized from a mixed solvent of hexane and ethyl acetate to yield 1.43 g (70.1%) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07851473B2 |
|---|
| Source dataset | uspto-grants-2010_12 |
|---|
| ORD ID | ord-f6708f12a54e4d34a6c9fa1c793c85af |
|---|
| Source note | uspto-grants-2010_12 |
|---|