Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 70175750 | HCID 70175750 | — |
| Product | HCID 70174515 | HCID 70174515 | — |
Reaction Steps
8.8 g of (3R,4R)-1-benzoyl-4-[3-(6-methoxyquinolin-4-yl)propyl]piperidine-3-carboxylic acid were heated, with stirring, in 200 cm3 of 5N aqueous hydrochloric acid at a temperature in the region of 100° C. for 48 hours. The reaction mixture was concentrated under reduced pressure (5 kPa) at a temperature in the region of 50° C. The residue was taken up in 100 cm3 of acetone. The mixture was concentrated under reduced pressure (5 kPa) at a temperature in the region of 60° C. This operation was repeated an additional two times. The residue was finally triturated in 100 cm3 of acetone until it crystallized. After filtering off the crystals and drying in a desiccator under reduced pressure (10 kPa), 7.2 g of (3R,4R)-4-[3-(6-methoxyquinolin4-yl)propyl]piperidine-3-carboxylic acid hydrochloride were obtained in the form of a beige solid melting at approximately 270° C. (melting with softening).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06403610B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-e2aeb6f299ac49fe8d5e926e2e89b8b6 |
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| Source note | uspto-grants-2002_06 |
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