Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | (S)-5-methyl-3-nitromethyl-hexanoic acid ethyl ester | HCID 29984078 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Water | HCID 962 | — |
| Product | Pregabalin | HCID 5486971 | 61% |
Reaction Steps
150 g of (S)-5-methyl-3-nitromethyl-hexanoic acid ethyl ester (VIII, R1=ethyl; assay: 97.2%) were suspended in 300 mL of H2O. KOH (90.1.g, assay 86.1%, 2.05 eq.) was added. The initially turbid reaction mixture became clear which indicated that the reaction was nearly completed. After complete conversion (determined by HPLC) NH4-formate and Pd/C were added. The reaction mixture was stirred until complete conversion was observed. The solution was filtered and then concentrated to about 250 g under reduced pressure and 400 mL of 2-propanol were added. At a temperature of 45° C. acetic acid was added until a pH of 7.0 was reached. Pregabalin started to crystallize. Within about 60 minutes the reaction mixture was cooled down to 10° C. Stirring was continued for 1 hour, then the product was isolated by filtration. The filter cake was washed with 90 mL of a 1:1 mixture of cold H2O/2-propanol. After drying, 65 g of substantially pure pregabalin (purity 97.9%) were obtained (yield: 61%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546112B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-d6a39975a66949c7a147349cb1adb027 |
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| Source note | uspto-grants-2013_10 |
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