Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 69252175 | HCID 69252175 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 69252172 | HCID 69252172 | — |
Reaction Steps
Cyclopentyl methyl 2-(6-aminopyridin-3-ylmethyl)-2-(1-cyclopentyl-1H-imidazol-4-yl)malonate (0.30 g; 0.57 mmol) was dissolved in absolute ethanol (5 ml). At 0° C., ethanolic HCl was added. The reaction solution was left to stand at 10° C. for 48 h. It was then concentrated under reduced pressure and the residue was taken up in 2N HCl. It was heated in a microwave (3×4 min; 180° C.). This was followed by washing with EA, and the aqueous phase was neutralized with 1N NaOH and then freeze-dried. The residue was taken up in methanol and filtered twice through a cartridge (C18). Concentration of the filtrate under reduced pressure resulted in 0.10 g of 3-(6-aminopyridin-3-yl)-2-(1-cyclopentyl-1H-imidazol-4-yl)-propionic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710232B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-8eafa7900ad7443fa7274a416eec0618 |
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| Source note | uspto-grants-2014_04 |
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