HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methyl-4-(4-nitro-3-(piperidin-1-yl)phenyl)piperazine → 4-(4-Methylpiperazin-1-yl)-2-(piperidin-1-yl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methyl-4-(4-nitro-3-(piperidin-1-yl)phenyl)piperazine | HCID 2885704 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(4-Methylpiperazin-1-yl)-2-(piperidin-1-yl)aniline | HCID 68679696 | 88.5% |
Reaction Steps
1-(5-Fluoro-2-nitro-phenyl)-piperidine (100 mg, 0.44 mmol) was treated with N-methylpiperizine (3 mL) and heated to 80° C. overnight. The reaction was diluted with EtOAc (10 mL), washed with water (2×10 mL), dried (Na2SO4) and concentrated in vacuo to afford 118 mg (88%) of 1-methyl-4-(4-nitro-3-piperidin-1-yl-phenyl)-piperazine as an oil. The 1-methyl-4-(4-nitro-3-piperidin-1-yl-phenyl)-piperazine (22 mg, 0.07 mmol) was stirred with 13 mg 5% Pd—C in 1 mL of MeOH under H2 for 2 h. The mixture was filtered through SiO2, eluting with 10% MeOH—CHCl3, and the solvent was concentrated in vacuo to give 17 mg (86%) of the title compound as a white solid. Mass spectrum (ESI, m/z): Calcd. for C16H26N4, 275.22 (M+H), found 275.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07705042B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-5e116b00b61b4ce28e5987071748db15 |
| Source note | uspto-grants-2010_04 |