HuagongsheHuagongshe Chemistry Print Report · For research reference only
Gabapentin → Piperidinium 1-{(1-Methyl-2-(Ethoxycarbonyl)-3-Ethoxy-3-Oxoprop-1-enyl)aminomethyl}-1-C yclohexane Acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Gabapentin | HCID 3446 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 1,3-Diethyl 2-acetylpropanedioate | HCID 136365 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Piperidinium 1-{(1-Methyl-2-(Ethoxycarbonyl)-3-Ethoxy-3-Oxoprop-1-enyl)aminomethyl}-1-C yclohexane Acetate | HCID 22272000 | — |
Reaction Steps
Diethyl acetylmalonate (202 mg, 1 mmol), gabapentin (171 mg, 1 mmol), and piperidine (99 μL, 1 mmol) were mixed in anhydrous ethanol (10 mL). After heating under reflux for 16 h, the solvent was removed under reduced pressure to give the title compound with purity greater than 90%. 1H NMR (CDCl3, 400 MHz): δ 1.28 (t, J=7.2 Hz, 6H), 1.38-1.64 (m, 12H), 1.75 (m, 4H), 1.96 (s, 3H), 2.23 (s, 2H), 2.99 (m, 4H), 3.24 (d, J=5.2 Hz, 2H), 4.20 (q, J=7.2 Hz, 4H), 4.35 (s, br, 2H), 7.79 (t, J=5.2 Hz, 1H). MS (ESI) m/z 354.38 (M−H−).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06972341B2 |
| Source dataset | uspto-grants-2005_12 |
| ORD ID | ord-1a8aa56f66064928a9b65ba53021205d |
| Source note | uspto-grants-2005_12 |