HuagongsheHuagongshe Chemistry Print Report · For research reference only
Gabapentin → Gabapentin Enacarbil
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Gabapentin | HCID 3446 | — |
| Reactant | [(1-Isobutanoyloxyethoxy)carbonyloxy]succinimide | HCID 66743414 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | Gabapentin Enacarbil | HCID 9883933 | 101.2% |
Reaction Steps
To a solution of gabapentin (6.8 g, 0.04 mole) in water (40 mL) is added a solution of [(1-isobutanoyloxyethoxy)carbonyloxy]succinimide (10 g, 0.036 mol) in acetonitrile (40 mL) over a period of 30 minutes. The reaction is stirred at ambient temperature for 3 hours. The reaction mixture is diluted with methyl tert-butyl ether (200 mL), washed with water (2×100 mL) and brine (50 mL). The organic phase is separated, dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo to afford the title compound as a white solid (12 g, quantitative).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08026279B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-2850feb1ba9f46dd99853ed56947bc4b |
| Source note | uspto-grants-2011_09 |