Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 131723278 | HCID 131723278 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | HCID 70172163 | HCID 70172163 | — |
Reaction Steps
A solution of 0.2 g of methyl (3R,4R)-4-[3-(R,S)-fluoro-3-(6-methoxyquinolin-4-yl)propyl]-1-[2-(2-thienylthio)ethyl]piperidine-3-carboxylate in 3 cm3 of 6N aqueous hydrochloric acid was heated with stirring at a temperature in the region of 100° C. for 7 hours and then evaporated under reduced pressure (5 kPa) at a temperature in the region of 50° C. The residue obtained was stirred in 10 cm3 of diisopropyl ether. The crystals which resulted therefrom were filtered off, washed with 2 times 5 cm3 of diisopropyl ether, and dried under reduced pressure (13 Pa) at a temperature in the region of 60° C. 0.22 g of (3R,4R)-4-[3-(R,S)-fluoro-3-(6-methoxyquinolin-4-yl)propyl]-1-[2-(2-thienylthio)ethyl]piperidine-3-carboxylic acid dihydrochloride were obtained in the form of a solid with a beige color melting with softening at a temperature in the region of 140° C.
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-a026272103784df9870f53edeb791f71 |
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| Source note | uspto-grants-2002_06 |
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