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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28765Generated: October 25, 2026

Gabapentin → Boc-Asp(OMe) Gabapentin

https://huagongshe.com/reaction/28765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGabapentinHCID 3446—
ReactantN-HydroxysuccinimideHCID 80170—
ReactantSodium BicarbonateHCID 516892—
Reactant(2S)-2-{[(tert-butoxy)carbonyl]amino}-4-methoxy-4-oxobutanoic acidHCID 10977771—
SolventAcetonitrileHCID 6342—
ProductBoc-Asp(OMe) GabapentinHCID 13172701398%

Reaction Steps

To a solution of Boc-Asp(OMe)-OH (5 g, 20 mmol) in acetonitrile (100 mL) was added N-hydroxysuccinimide (2.53 g, 22 mmol) and N,N-dicyclohexylcarbodiimide (4.5 g, 22 mmol). The reaction was stirred at ambient temperature for 4 h. The reaction mixture was filtered directly into an aqueous solution (100 mL) of gabapentin (3.77 g, 22 mmol) and sodium hydrogencarbonate (1.85 g, 22 mmol) and the resulting mixture stirred at ambient temperature for 16 h. The reaction was concentrated under reduced pressure, the residue dissolved in ethyl acetate/diethyl ether (1:1, 300 mL) and washed with 0.1M aqueous potassium hydrogensulfate (2×500 mL). The organic phase was separated, dried over Na2SO4, filtered, and concentrated to dryness under reduced pressure to afford Boc-Asp(OMe)-Gabapentin as a white solid (7.8 g, 19.5 mmol, 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420002B2
Source datasetuspto-grants-2008_09
ORD IDord-a5352857d5b9435d9c482e161179277d
Source noteuspto-grants-2008_09