Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Gabapentin hydrochloride | HCID 6453919 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Gabapentin | HCID 3446 | — |
Reaction Steps
In this Example, gabapentin hydrochloride was dissolved in 130 ml of dry isopropanol at 25° C. Then 1.1 grams of active carbon was added and the suspension was heated to 40° C. and maintained at this temperature for 2 hours. The suspension was filtered at 40° C. and the filter cake was then washed twice, each time with an additional 15 ml of isopropanol. The washings were added to the already separated solution of gabapentin hydrochloride in isopropanol. After half an hour of mixing at 25° C., 19.5 grams of tributylamine was added during half an hour and the mixing was continued for two hours at the same temperature. The formed gabapentin base was separated from the suspension by filtration and washed with 23 ml of methanol to give gabapentin crude. After reslurry as in Example 1B gabapentin pure was obtained at a yield of 58.8% and chloride anion content of 7 ppm Cl−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06531509B2 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-c8598b15ddfa41c08c4519ec94850dac |
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| Source note | uspto-grants-2003_03 |
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