HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pregabalin → Pregabalin Impurity 25
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pregabalin | HCID 5486971 | — |
| Reactant | Ethyl 5-methylhex-2-enoate | HCID 6436900 | — |
| Reactant | Ethyl 5-methyl-3-(nitromethyl)hexanoate | HCID 14463328 | — |
| Solvent | Nitromethane | HCID 6375 | — |
| Product | Pregabalin Impurity 25 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08466297B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-909f1483f5ff4107b88b28915ed07aa4 |
| Source note | uspto-grants-2013_06 |