HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrobenzaldehyde → 1,1-Dimethylethyl (2R)-2-methyl-4-[(4-nitrophenyl)methyl]-1-piperazinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrobenzaldehyde | HCID 541 | — |
| Reactant | (R)-tert-butyl 2-methylpiperazine-1-carboxylate hydrochloride | HCID 45072184 | — |
| Reactant | 1,1-Dimethylethyl (2S)-2-methyl-4-[(4-nitrophenyl)methyl]-1-piperazinecarboxylate | HCID 59262204 | — |
| Product | 1,1-Dimethylethyl (2R)-2-methyl-4-[(4-nitrophenyl)methyl]-1-piperazinecarboxylate | HCID 59262157 | — |
Reaction Steps
The title compound was prepared from 4-nitrobenzaldehyde and 1,1-dimethylethyl (2R)-2-methyl-1-piperazinecarboxylate hydrochloride using a method similar to that described for D1 in Description 1. MS (ES+): 280.2, 236.3, no molecular ion (MH+) observed
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700599B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-fdec3d1203b742de8dff1db72887c06c |
| Source note | uspto-grants-2010_04 |