HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419425Generated: October 30, 2026
Ethyl Acetate → 4-{4-[4-(2-Fluoroethyl)-1-piperazinyl]-1-piperidinyl}-2,5-bis(methyloxy)aniline
https://huagongshe.com/reaction/419425
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1-{1-[2,5-Bis(methyloxy)-4-nitrophenyl]-4-piperidinyl}-4-(2-fluoroethyl)piperazine | HCID 59452919 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-{4-[4-(2-Fluoroethyl)-1-piperazinyl]-1-piperidinyl}-2,5-bis(methyloxy)aniline | HCID 59452685 | — |
Reaction Steps
1-{1-[2,5-Bis(methyloxy)-4-nitrophenyl]-4-piperidinyl}-4-(2-fluoroethyl)piperazine (1.36 g, 3.43 mmol) was taken up in EtOH (50 mL) and EtOAc was added to help with solubility. The catalyst, 5% sulfided platinum on carbon (140 mg) was added. The reaction was placed on a Fischer-Porter Hydrogenator under 50 psi of H2 gas and was allowed to stir at rt overnight. The catalyst was filtered off and the filtrate was concentrated in vacuo to give the title compound of step F without further purification (1.2 g, 95%). 1H NMR (400 MHz, DMSO-d6) δ ppm 6.42 (s, 1H), 6.28 (s, 1H), 4.53 (t, J=4.9 Hz, 1H), 4.41 (t, J=4.9 Hz, 1H), 4.31 (s, 2H), 3.63 (s, 3H), 3.61 (s, 3H), 3.15 (s, 2H), 2.57 (t, J=4.8 Hz, 1H), 2.49-2.51 (m, 1H), 2.45-2.48 (m, 6H), 2.42 (d, J=13.4 Hz, 4H), 2.17 (t, J=11.3 Hz, 1H), 1.73 (d, J=11.0 Hz, 2H), 1.46 (qd, J=11.7, 3.5 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08093239B2 |
|---|
| Source dataset | uspto-grants-2012_01 |
|---|
| ORD ID | ord-08ac9a82f39f4629a6a97bf2acdeec01 |
|---|
| Source note | uspto-grants-2012_01 |
|---|