HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl 4-(Isopropylcarbamoyl)piperazine-1-carboxylate → N-Isopropylpiperazine-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl 4-(Isopropylcarbamoyl)piperazine-1-carboxylate | HCID 86719361 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-Isopropylpiperazine-1-carboxamide | HCID 16740267 | 130.4% |
Reaction Steps
To a solution of benzyl 4-(isopropylcarbamoyl)piperazine-1-carboxylate (3, 3.94 g, 12.9 mmol) in methanol (100 mL) was added 10% Pd/C (50% wet, 0.400 g) and the mixture was stirred under 1 atmosphere of hydrogen for 16 h. After this time, the mixture was filtered through Celite and the filtrate concentrated to afford the title compound (2.88 g, >99%): 1H NMR (300 MHz, CD3OD) δ 4.00-3.80 (m, 1H), 3.45-3.35 (m, 4H), 2.88-2.78 (m, 4H), 1.13 (d, J=6.5 Hz, 6H); Multimode MS m/z 172 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09278940B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-f64017b7a1b545a3a8b4402028b3b5a5 |
| Source note | uspto-grants-2016_03 |