Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259442Generated: November 1, 2026

Pregabalin → Pregabalin Impurity 25

https://huagongshe.com/reaction/1259442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPregabalinHCID 5486971—
ReactantEthyl 5-methylhex-2-enoateHCID 6436900—
ReactantEthyl 5-methyl-3-(nitromethyl)hexanoateHCID 14463328—
SolventNitromethaneHCID 6375—
ProductPregabalin Impurity 25HCID 24938718—

Reaction Steps

In Synthesis 1989, 953 a synthesis of rac.-Pregabalin, starting from (E)-5-methyl-hex-2-enoic acid ethyl ester, which was converted with nitromethane into 5-methyl-3-nitromethyl-hexanoic acid ethyl ester, has been reported. Subsequent catalytic hydrogenation followed by saponification leads to rac.-Pregabalin. Recently an enzymatic hydrolysis of this racemic nitro ester was carried out (Tetrahedron Asymmetry 2008, 19, 945). With enzyme Novozyme 435 enantiomerically enriched (S)-5-methyl-3-nitromethyl-hexanoic acid could be obtained in a good selectivity if the conversion was stopped at 30%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466297B2
Source datasetuspto-grants-2013_06
ORD IDord-909f1483f5ff4107b88b28915ed07aa4
Source noteuspto-grants-2013_06