HuagongsheHuagongshe Chemistry Print Report · For research reference only
Gabapentin → HCID 71737521, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Gabapentin | HCID 3446 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Methyl 1-cyano-4-hydroxy-7-phenoxyisoquinoline-3-carboxylate | HCID 89812860 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | HCID 71737521 | HCID 71737521 | — |
Reaction Steps
Methyl 1-cyano-4-hydroxy-7-phenoxyisoquinoline-3-carboxylate (30 mg, 0.09 mmol), gabapentin (96 mg, 0.56 mmol, TCI) and sodium methoxide (28 mg, 0.53 mmol) were suspended in 2-methoxyethanol (3 mL). The resulting mixture was heated to reflux for 3 hours and then cooled to room temperature. The solvent was removed in vacuo and the residue was dissolved in H2O (15 mL) and EtOAc (15 mL). To the stirred mixture was added 1 N hydrochloric acid until pH was 1. The layers were separated and the aqueous layer was extracted twice with EtOAc. The combined organic layers were dried over MgSO4, concentrated, and purified by flash chromatography (0-50% EtOAc/hexanes with 0.5% formic acid) to give the title compound in 11 mg. MS: (−) m/z 458.00 (M-1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09409892B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-d72e24c4ef2b477387502da53bd2f2b5 |
| Source note | uspto-grants-2016_08 |