HuagongsheHuagongshe Chemistry Print Report · For research reference only
(S)-tert-Butyl 2,4-dibenzylpiperazine-1-carboxylate → 1,1-Dimethylethyl (2S)-2-(phenylmethyl)-1-piperazinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (S)-tert-Butyl 2,4-dibenzylpiperazine-1-carboxylate | HCID 22884141 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | 1,1-Dimethylethyl (2S)-2-(phenylmethyl)-1-piperazinecarboxylate | HCID 17750441 | — |
Reaction Steps
The title compound was prepared according to the procedure described in Example 2, Step C, except using 1-tert-butoxycarbonyl-2(S),4-dibenzylpiperazine (4.78 g, 11.3 mmol) and 10% palladium on carbon (1.04 g). The title compound was obtained as an oil. NMR (300 MHz, CD3OD) δ 7.25 (5H, m), 4.35 (1H, m), 4.00 (1H, d, J=12 Hz), 2.7-3.3 (7H, m), 1.25 (9H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05736539 |
| Source dataset | uspto-grants-1998_04 |
| ORD ID | ord-72949014fd5c48669a27eb5d4127551f |
| Source note | uspto-grants-1998_04 |