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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1991396Generated: October 26, 2026

Gabapentin → Boc-Asp(OMe) Gabapentin

https://huagongshe.com/reaction/1991396

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 μL) 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 numberUS07645797B2
Source datasetuspto-grants-2010_01
ORD IDord-f67849de4d7149c1919aa0f53f817fe8
Source noteuspto-grants-2010_01