Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767289Generated: October 26, 2026

Ammonium formate → Gabapentin Enacarbil

https://huagongshe.com/reaction/1767289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantAllyl 1-{[(alpha-Isobutanoyloxyethoxy)carbonyl]aminomethyl}-1-Cyclohexane AcetateHCID 9999163—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductGabapentin EnacarbilHCID 9883933—

Reaction Steps

To a stirred suspension of ammonium formate (3.4 g, 54 mmol) in ethanol (34 mL), was added compound (15) (10 g, 27 mmol) together with 10% Pd/C (1 g) under a nitrogen atmosphere. After one hour, the reaction mixture was filtered and the catalyst washed with ethanol (2×10 mL). The filtrates were combined and evaporated. The crude product was dissolved in diethyl ether (150 mL) and the organic phase was washed with 2N HCl (100 mL), water (100 mL) and brine (100 mL). The ether layer was dried over anhydrous sodium sulfate and concentrated to give a viscous liquid that crystallized upon standing. The product was recrystallized using 1:10 ethyl acetate:heptane (100 mL) to give the product (11) as a white, crystalline solid (7.9 g, 88%), m.p 63–64° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07232924B2
Source datasetuspto-grants-2007_06
ORD IDord-2f6a36ef9d804b6f8ca88b24d51148a4
Source noteuspto-grants-2007_06