Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 54098214 | HCID 54098214 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 54445967 | HCID 54445967 | 82.9% |
Reaction Steps
678 mg of 6-(L-lysylamino) 3-heptenedioic acid prepared as in Example 9 were dissolved at ambient temperature in 70 ml of ethanol and 2.1 ml of N hydrochloric acid and then 140 mg of palladium on active carbon were added, followed by hydrogenation under 1100 millibars for an hour and a half. The residue, after filtering, was evaporated to dryness, rinsed with ethanol then with water, dried and concentrated to dryness under reduced pressure. The residue was dissolved in water, and the pH was adjusted to 6 with ammonium hydroxide. The mixture was purified by passing through Dowex 50 W×8 ion-exchange resin and eluting with water and then with 0.5N ammonia, evaporation to dryness and lyophilized to obtain 566 mg of the expected product with a specific rotation of [α]D =+29°±1.5° (c=0.7% in H2O).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05030715 |
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| Source dataset | uspto-grants-1991_07 |
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| ORD ID | ord-58b04b9734e2483f9741f015fe207c66 |
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| Source note | uspto-grants-1991_07 |
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