HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclobutanone → Tert-butyl 4-(4-(1-cyanocyclobutylamino)phenyl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclobutanone | HCID 14496 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | tert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylate | HCID 11011301 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl 4-(4-(1-cyanocyclobutylamino)phenyl)piperazine-1-carboxylate | HCID 67132054 | 84% |
Reaction Steps
Trimethylsilyl cyanide (0.3 g, 3 mmol) was added dropwise to a mixture of 43a (0.415 g, 1.5 mmol), cyclobutanone (0.21 g, 3 mmol) and sodium sulfate (1 g) in dichloromethane (5 ml). The mixture was stirred for 15 hours. After filtration to eliminate sodium sulfate, the medium was concentrated under vacuum to obtain a brown liquid which was subjected to chromatography (dichloromethane:acetone, 75:25) to yield 43b (0.448 g, 1.26 mmol, 84%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07709517B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-9a187d1afed64627b25c50988e892a7e |
| Source note | uspto-grants-2010_05 |