HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419395Generated: October 31, 2026
HCID 59452626, compound → HCID 59452728, compound
https://huagongshe.com/reaction/419395
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 59452626 | HCID 59452626 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59452728 | HCID 59452728 | 63.4% |
Reaction Steps
To 1-[3-(methyloxy)-4-nitrophenyl]-4-{1-[2-(methylsulfonyl)ethyl]-4-piperidinyl}piperazine (1.18 g, 2.76 mmol) in EtOAc (100 mL) and EtOH (25 mL) was added Pd on carbon in one portion. The mixture was stirred at rt under H2 (1 atm.) until complete by TLC. The reaction was filtered through Celite® and concentrated. Purification by flash chromatography provided the title compound of step F (0.690 g, 1.75 mmol, 63%). 1H NMR (400 MHz, DMSO-d6) δ ppm 1.31-1.42 (m, 2H), 1.75 (d, J=11.4 Hz, 2H), 1.86-1.97 (m, 2H), 2.15 (tt, J=11.3, 3.9 Hz, 1H), 2.54-2.59 (m, 4H), 2.65 (t, J=6.8 Hz, 2H), 2.88-2.94 (m, 6H), 3.00 (s, 3H), 3.25 (t, J=6.8 Hz, 2H), 3.71 (s, 3H), 4.18 (br. s., 2H), 6.25 (dd, J=8.4, 2.6 Hz, 1H), 6.46 (d, J=2.6 Hz, 1H), 6.49 (d, J=8.4 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08093239B2 |
|---|
| Source dataset | uspto-grants-2012_01 |
|---|
| ORD ID | ord-8f9520eb857c4566aa46a0235301c1a2 |
|---|
| Source note | uspto-grants-2012_01 |
|---|